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"Defek tulang luas belum memiliki solusi memuaskan walaupun dengan kemajuan teknik operasi dan agen biologis terbaru. Penggunaan sel punca mesenkimal (SPM) menunjukkan proliferasi dan diferensiasi minimal pasca implantasi. Sekretom dapat menjadi alternatif SPM sebagai produk siap pakai dengan efek osteoinduktor yang poten. Penelitian ini bertujuan untuk mengetahui efek sekretom pada penyembuhan defek luas tulang panjang pada tikus Sprague Dawley (SD) secara radiologis dan histologis. Sebanyak 60 ekor tikus SD dibagi menjadi 5 kelompok yaitu kontrol, SPM, sekretom, SPM+sekretom, dan SPM+sekretom+BMP-2. Setelah 2 dan 4 minggu, dilakukan pemeriksaan radiologis dengan skor RUST (Radiographic Union Score for Tibial) dan histomorfometri dengan Image J (total kalus, area penulangan, tulang rawan, fibrosis, dan void). Pada berbagai pasase dan waktu, BMP-2 hanya terdapat dalam kadar yang sangat kecil di dalam sekretom. Pemberian sekretom lebih superior pada kelompok lain secara radiologis dan histomorfometris pada setiap waktu. Pemberian sekretom mengandung banyak faktor pertumbuhan dan sitokin yang dapat mempercepat dan meningkatkan penyembuhan tulang. Implantasi SPM xenogenik dapat memperpanjang proses inflamasi pada dan kombinasinya dengan sekretom memberikan efek toksistas terhadap penyembuhan tulang Sekretom, baik digunakan secara tunggal maupun kombinasi dengan SPM dan BMP-2 merupakan agen osteoinduktor baru yang poten dalam perbaikan tulang pada model tikus dengan defek tulang luas.

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Critical sized defect (CSD) has been a problem despite advanced surgical techniques and new biologic agent. Recent literatures have shown that bone marrow derived Mesenchymal Stem Cell (BM-MSC) proliferate and differentiate only in a small amount upon implantation. Meanwhile secretome which previously was considered as waste product during MSC culture, may now presents considerable advantages over living cells in terms of potency, manufacturing, storage, cost, and potential as a ready-to-go osteoinductor agent. The study aimed to determine the effect of secretome in the healing of CSD SD (Sprague Dawley) rat by radiographic and histologic analysis. A total of 60 SD-rat were divided into 5 groups including, control (normal saline), MSC, secretome, MSC+secretome, MSC+secretome+BMP-2. After 2 and 4 weeks, RUST (Radiographic Union Score for Tibia) and histomorphometric (callus, osseous, cartilage, fibrous and void area) evaluation using Image J are compared. Secretome group is superior to other group significantly in all parameters at all time. Implantation of xenogenic MSC might prolong the inflammation phase of bone healing while the MSC+secretome group suggest the toxicity effect decreasing the bone formation area. Secretome, whether used solely or combined with BM-MSC and BMP-2, is a novel, potent bone-healing agent for CSD in rat models."

"Latar Belakang: Penatalaksanaan defek tulang dengan terapi regeneratif seperti penggunaan sekretom berpotensi mengatasi kekurangan, seperti morbiditas donor, dari pencangkokan tulang autologus. Namun hingga saat ini belum ada penelitian yang meneliti perbedaan kemampuan pertumbuhan tulang dari sekretom asal sel punca tali pusat, jaringan lemak, dan sumsum tulang. Metode: Penelitian ini adalah penelitian eksperimental hewan menggunakan 63 tikus, dibagi menjadi 5 kelompok besar, yaitu kelompok sekretom sel punca mesenkimal (SPM) asal tali pusat, jaringan lemak, sumsum tulang, kontrol tanpa tindakan, dan kontrol dengan hidroksiapatit. Setiap tikus dioperasi sesuai dengan tindakannya, kelompok perlakuan diberi perlakuan sekretom yang sesuai dan hidroksiapatit dan kemudian kalus yang terbentuk diperiksa 2 minggu kemudian. Pemeriksaan luaran menggunakan histopatologi, berupa histomorfometri (area penulangan, fibrosis dan kartilago) dan pulasan immunohistokimia Bone Morphonegetic Protein (BMP)-2, dan pemeriksaan Enzyme Linked Immunoabsorbent Assay (ELISA) protein Indian Hedgehog (Ihh). Hasil: Kelompok yang mendapatkan sekretom asal SPM jaringan lemak memiliki area penulangan terbanyak, sedangkan kedua kelompok kontrol terendah (p<0,001), kelompok sekretom asal SPM sumsum tulang memiliki area kartilago terbanyak (p=0,134), dan kedua kelompok kontrol memiliki area fibrosa terbanyak (p=0,198). Skor BMP-2 tertinggi tampak pada kelompok sekretom asal SPM adiposa dan paling rendah pada kelompok kontrol (p<0.001). Kadar protein Ihh secara bermakna paling tinggi pada kelompok sekretom asal SPM sumsum tulang, dan paling rendah pada kelompok kontrol (p<0.001)Kesimpulan: Sekretom memiliki kemampuan osteogenitas, dengan sekretom asal SPM jaringan adiposa yang memiliki kemampuan penulangan tertinggi pada tikus dengan defek tulang kritis, dibandingkan dengan kelompok sekretom lainnya dan kelompok yang tanpa diberikan tindakan

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Introduction: The management of bone defects with regenerative therapy using a secretome, for example, is promising and potentially may outweigh the shortcoming of autologous bone graft therapy such as donor morbidity. However, not many studies have compared the differences in the capabilities of bone growth from secretome derived from umbilical cord, adipose and bone marrow stem cell.

Methods: This research is an experimental animal study using 63 rats. A total of 63 rats were divided into 5 major groups (umbilical cord, adipose, bone marrow stem cell secretomes, control without treatment, and control with hydroxyapatite). Each mice was treated accordingly and the harvesting was done after 2 weeks. All samples were examined histopathologically using histomorphometry (ossification, fibrosis, and cartilage area) and Bone Morphogenetic Protein (BMP)-2 immunohistochemistry staining and Enzyme Linked Immunoabsorbent Assay (ELISA) Indian Hedgehog (Ihh) protein

Results: The percentage of ossification area was significantly highest in the adipose stem cell secretome group, and the lowest in both control group (p<0.001). The highest percentage of cartilage area was seen in the bone marrow stem cell secretome group (p=0.134) and the highest percentage of fibrous area was seen in both control group (p=0.198). The highest BMP-2 score was seen in the adipose stem cell secretome group and the lowest was in the control group (p<0.001). Level of Ihh protein was significantly highest in the bone marrow stem cell group group and lowest in the control group (p<0.001)

Conclusion: Secretome had osteogenic inducing ability, with adipose stem cell-derived secretomes having the highest bone density in mice with critical bone defects, compared to the other secretome groups and the control group."

"Diabetes melitus (DM) menyebabkan gangguan saraf autonom, sensorik, dan motorik, terutama di kaki dan pergelangan kaki yang menyebabkan perubahan postur kaki dan deformitas. Artritis pergelangan kaki penyandang DM mengakibatkan gangguan fungsional sehingga artrodesis merupakan suatu opsi tata laksana pembedahan. Sayangnya, gangguan metabolik DM mengakibatkan komplikasi yang tak jarang yakni non-union. Terapi sel dan derivatnya merupakan opsi terapi regeneratif untuk meningkatkan kesembuhan tulang.Pembuatan model artritis hewan DM dengan injeksi streptozotosin (STZ), diet tinggi lemak (HFD), dan injeksi complete freud adjuvant (CFA) dilanjutkan studi eksperimental in vivo dengan fokus hasil augmentasi fusi dengan granul hidroksiapatit (HA), sel punca mesenkimal asal tali pusat (SPM-TP), dan sekretom jaringan adiposa (JA). Sebanyak 16 sampel kaki dibagi menjadi 3 kelompok: kontrol negatif (kelompok 1), kontrol positif yang diberikan autologous bone graft (kelompok 2), dan perlakuan yang diberikan HA, SPM-TP, dan sekretom-JA (kelompok 3). Dilakukan evaluasi parameter klinis, radiologis, profil histomorfometris, dan ekspresi biomarker di subjek model artritis DM tikus Sprague Dawley (SD).Status DM tercapai setelah induksi STZ dengan rerata kadar glukosa 421 ± 27,16 mg/dL. Kelompok artritis menunjukkan perubahan diameter ankle yang bermakna dibanding kontrol serta perubahan radiologis sendi pergelangan kaki. Artritis berat (skor 3) ditemukan di mayoritas (80%) sampel kelompok 1 yang merupakan kontrol negatif (hanya induksi DM). Kelompok perlakuan menunjukkan skor artritis terendah serta osifikasi di sisi anterior tibiotalar. Terdapat perbedaan bermakna osteokalsin (p = 0,017) dan gen chordin (p = 0,003) antara ketiga kelompok.Simpulan: Model artritis DM pada tikus SD berhasil dibuat dengan injeksi STZ dan HFD serta induksi artritis kronik dengan injeksi CFA di sendi pergelangan kaki selama 4 minggu. Pemberian SPM-TP, sekretom JA, dan granul HA menunjukkan skor artritis yang lebih rendah. Namun, pemberian ketiga bahan tersebut tidak menghasilkan gambaran fusi yang lebih baik, serta tidak meningkatkan kadar osteokalsin, namun menghasilkan jumlah chordin (protein inhibisi BMP) yang lebih kecil dibandingkan baku standar.

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Diabetes mellitus (DM) can cause disturbances in the autonomic, sensory, and motor nerves, particularly in the feet and ankles, eventually leading to changes in foot posture and specific deformities. The advancement of management using stem cells and their secretome has shown promising outcomes. A model of DM arthritis can be created by inducing experimental animals with streptozotocin (STZ). In the DM arthritis model, the evaluation of ankle arthrodesis augmented with umbilical cord mesenchymal stem cell (MSC-Uc) and adipose tissue secretome (Secretome-AD) can be carried out to observe the existing outcomes.

This study is divided into two stages wherein the first stage involves creating an arthritis model in DM animals. The study utilizes a pretest-posttest design to measure clinical and laboratory parameters before and after treatment. Subsequently, the second stage involves an in vivo experimental study focusing on the outcomes of fusion augmentation with MSC-Uc, secretom-AD, and HA granule. The second stage of the study includes assessments using single-blinding methods for clinical, radiological, histomorphometric profile, and biomarker expression in the SD rat model of DM arthritis.

DM status was achieved after STZ injection, with an average glucose level of 421 ± 27.16 mg/dL. The final diameter averages in groups 1 – 3, which were not induced with arthritis (9.64 ± 0.49 mm), significantly differed from group 4 (12.50 ± 0.87 mm, p = 0.003) and 5 (11.85 ± 0.74 mm, p = 0.037). The arthritis groups showed radiological changes in the ankle joint. After modeling, there was a significant increase in fasting blood glucose compared to pre-modeling measurements. Severe arthritis (score 3) was found in the majority (80%) of samples in group 1, which served as the negative control (DM induction only). Anova test results for the IHC parameter showed significant differences (p = 0.017) in osteocalcin and chordin gene (p = 0.003) among the three groups.

Conclusion: A model of DM arthritis in SD rats was successfully created by STZ and HFD induction, followed by the induction of chronic arthritis with CFA injection in the ankle joint for 4 weeks. The administration of MSC-Uc, secretome-AD, and HA granule indicated lower arthritis scores. However, the administration of these three substances did not produce a better fusion picture, nor did it increase osteocalcin levels, but it resulted in a smaller amount of chordin (BMP inhibition protein) compared to the standard."

"Pendahuluan: Efek hiperglikemik dan produk Advanced Glycation Endproduct (AGE) dari diabetes mellitus (DM) sering dikaitkan dengan komplikasi muskuloskeletal seperti neuropati perifer dan tendinopati Achilles pada regio pergelangan kaki. Hal ini beresiko menimbulkan efek lanjutan berupa perubahan struktur berjalan, kekakuan sendi hingga luka tukak telapak kaki. Tatalaksana tendinopati DM hingga saat ini terbatas pada pengurangan gejala lanjutan tanpa meningkatkan proses regenerasi tendon, sehingga dibutuhkan penelitian untuk menilai efek terapi dari sekretom dan eksosom SPM dalam hal perbaikan struktur tendon. Hal ini diwakili oleh penggunaan hewan coba tikus SD yang telah terinduksi menjadi tendinopati DM. Metode: Studi ini melibatkan fase studi pilot pertama, kedua, dan penelitian utama. Tikus SD diperoleh dan diberikan diet tinggi lemak (HFD) dan pemberian larutan fruktosa 55% selama delapan minggu. Diabetes diinduksi menggunakan injeksi streptozotocin (STZ) intraperitoneal berbagai dosis. Studi pilot pertama bertujuan untuk menentukan volume cairan yang dapat diinjeksikan ke area peritendon. Sementara itu, studi pilot kedua bertujuan untuk mengidentifikasi dosis STZ yang efektif. Dalam fase penelitian utama, tikus diabetes menerima injeksi lokal eksosom, sekretom, atau kombinasinya. Setelah perawatan, tikus dieutanasia, dan tendon Achilles dianalisis secara histopatologi dan imunohistokimia. Hasil dan Diskusi: Studi pilot pertama menyimpulkan bahwa 0,8 ml merupakan volume cairan optimal yang dapat diinjeksikan ke area peritendon. Sementara itu, studi pilot kedua menunjukkan bahwa setelah 8 minggu HFD, pemberian fruktosa, dan injeksi STZ, kelompok STZ 26 mg/kg memiliki kadar glukosa 220,54 ± 9,11 mg/dL, dan kelompok STZ 30mg/kg memiliki 213,88 ± 8,99 mg/dL dengan perbedaan paling signifikan dalam skor Bonar diamati di kelompok STZ 30mg/kg, hal ini menunjukkan keberhasilan induksi hewan coba. Pada penelitian utama setelah pemberian sekretom, eksosom, atau kombinasi, kadar TGF-β dan IL-6 dan skor Bonar tidak menunjukkan perbedaan signifikan antar kelompok. Analisis pasca intervensi mengungkapkan perbedaan signifikan dalam kadar IL-6 dan Col-1, dimana pada kelompok perlakuan terdapat penurunan IL-6 yang signifikan pada hari ke-14 dan peningkatan Col-1 yang signifikan pada hari ke-21 dibandingkan dengan kelompok kontrol. Kesimpulan: Penelitian ini menunjukkan bahwa kombinasi diet HFD, pemberian fruktosa, dan dosis injeksi STZ 30 mg/kg efektif menciptakan hewan model tendinopati DM. Skor Bonar yang tinggi pada kelompok STZ mengindikasikan kerusakan tendon signifikan. TGF-β dan IL-6 tidak menunjukkan perbedaan signifikan antar kelompok, namun IL-6 meningkat pada hari ke-14 dan Col-1 pada hari ke-21 pada kelompok intervensi secara signifikan, menunjukkan potensi terapi eksosom dan sekretom pada penyembuhan tendon.

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Introduction: The hyperglycemic effects and Advanced Glycation Endproduct (AGE) of diabetes mellitus (DM) are often associated with musculoskeletal complications such as peripheral neuropathy and Achilles tendinopathy in the region of the legs and ankles. It is one of the risks of developing advanced negative effects such as changes in walking structure, stiffness of the joints to ulcer wounds on the the ankle. The management of DM tendinopathy to date is limited to reducing advanced symptoms without enhancing tendon regeneration process, therefore, further research is needed to assess the therapeutic effects of MSC secretomes and exosomes in terms of tendon structure improvement. It is represented by the use of SD rats induced into DM

tendinopathy.

Methods: This study involves two pilot study phases and the main research. SD mice were obtained and given a high-fat diet (HFD) and given 55% fructose solution foreight weeks. Diabetes is induced by injection of streptozotocin (STZ). The first phase of the pilot study aims to determine the volume of liquid injected into the peritendon area, and the second phase aims to identify an effective dose of STZ to induce DM. In the main study, diabetic mice received local injections of exosomes, secretomes, or a combination of them. After treatment, the rats were euthanazied, and the Achilles tendon was analysed histopathologically and immunohistochemically.

Results and Discussion: The first pilot study concluded that 0.8 ml was the optimal fluid volume that could be injected into the peritendon area. Meanwhile, the second pilot study showed that after 8 weeks of HFD, fructose administration, and injection of STZ, the STZ 26 mg/kg group had a glucose level of 220.54 ± 9.11 mg/dL, and the STZ 30 mg/kg group had 213.88 ± 8.99 mg/dL with the most significant difference in Bonar score was observed in the STZ 30mg/kg group, this indicates successful induction of experimental animals. In the main study after administering secretome, exosome, or a combination of the two, the levels of TGF-β and IL-6 and the Bonar score did not show significant differences between groups. Post-intervention analysis revealed significant differences in IL-6 and Col-1 levels, in which the treatment group there was a significant decrease in IL-6 on day 14 and a significant increase in Col-1 on day 21 compared to the control group.

Conclusion: This study shows that a combination of HFD, fructose administration, and STZ 30mg/kg are effective in creating animal model for diabetic Achilles tendinopathy. A high Bonar score in the STZ group indicates significant tendon damage. TGF-β and IL-6 did not show significant differences between the groups, but IL-6 increased on day 14 and Col-1 on day 21 in the intervention groups significantly, indicating the potential for exosome and secretome therapy on tendon healing.

Keyword: diabetic Achilles tendinopathy, Sprague Dawley rats, exosome and secretome combination, bone marrow mesenchymal stem cel"

"Pendahuluan: Penelitian in vitro menggambarkan inferioritas osteogenesis SPM adiposa dibandingkan dengan SPM sumsum tulang. Sebaliknya, penelitian in vivo menunjukkan kemiripan potensi osteogenik keduanya. penelitian ini mencoba mengetahui perbedaan kapasitas osteogenik antara keduanya dengan mengukur ekspresi Bone Morphogenetic Protein (BMP)-2 dan BMP Reseptor II, juga proses penyembuhan tulang dengan pengukuran histomorfometri.Metode: Delapan belas tikus Sprague dawley (SD) dilakukan defek tulang femur 5mm. Tikus dibagi tiga kelompok yang terdiri dari kontrol, implantasi SPM sumsum tulang + Hydroxypatite, dan implantasi SPM adiposa + Hydroxypatite. Tikus dikorbankan pada minggu kedua kemudian penilaian histomorfometri kuantitatif dilakukan dengan Image-J. Paramater yang diukur adalah luas total kalus, % area penulangan, % area kartilago, dan % area fibrosis. Dilakukan penilaian imunohistokimia menggunakan intensitas pewarnaan dan skor Imunoreaktivitas (IRS).Hasil: Kelompok SPM sumsum tulang menunjukkan ekspresi BMPR II lebih tinggi dibandingkan kelompok lainnya. Ekspresi BMPR II dianalisis dan didapatkan hasil yang signifikan (p= 0,04) dengan median 4.00 ± 2.75. Kelompok SPM sumsum tulang dan adiposa juga menunjukkan proses penyembuhan tulang yang lebih baik dibandingkan kelompok kontrol (p = 0,001). Tidak ada perbedaan yang signifikan antara SPM sumsum tulang dan SPM adiposa yang diukur pada % total area kalus (p = 1.000),% area penulangan (p = 1.000),% kartilago (p = 0,493) dan % fibrosis (p = 0,128).Diskusi: SPM adiposa memiliki kemampuan penyembuhan tulang yang serupa dengan SPM sumsum tulang. Growth factor dan reseptornya penting namun bukan satu-satunya faktor penyembuhan tulang.

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Introduction: In vitro studies describe inferior osteogenesis of Adiposes to Bone Marrow Mesenchymal Stem Cell (MSC). Contrary, in vivo studies showing the resemblance of osteogenic potential between both groups. This study tries to investigate the difference of osteogenic capacity between BMSCs and ASCs by quantifying the expression of Bone Morphogenetic Protein (BMP)-2 and BMP receptor (BMPR) II also the bone healing process by histomorphometry measurement.Methods: Eighteen Sprague dawley (SD) rats were induced with 5mm femoral bone defect, then divided into three groups that consist of Control, Implementation of BMSC+Hydroxypatite, and Implementation of ASC+Hydroxypatite. They were sacrificed after 2 weeks, then performed histomorphometry assessment with Image-J. The measured paramater were total area of callus, % of osseous area, % of cartilage area, and % of fibrotic area. The immunohistochemistry measurement performed by staining intensity and immunoreactivity score (IRS).Results: The BMSC group showed higher expression of BMPR II compare to others. The expression of BMPR II was analyzed statistically and showed significant result (p=0.04) with median 4.00 ± 2.75. Both BMSC and ASC group have significantly better bone healing process compared with control group (p=0,001). There are no significant differences between ASC and BMSC measured in %total callus area (p=1.000), %Osseous area (p=1.000), %Cartilage area (p=0.493) and % Fibrous area (p=0.180). Discussions: ASC bone healing ability are similar to BMSC. Growth factor and its receptor are important but not sole contributing factor for bone healing."

"ABSTRAK Pendahuluan. Kesulitan dalam tatalaksana defek tulang yang luas merupakan salah satu tantangan dewasa ini. Selain tatalaksananya yang kompleks juga dapat memberikan dampak jangka panjang negatif yang berat. Penggunaan BMP-2 dalam tatalaksana fraktur dengan defek tulang yang luas memegang peranan penting. BMP-2 berperan pada proses osteogenesis dan chondrogenesis dan menghambat osteoclastogenesis melalui RANKL signaling. Penelitian ini bertujuan untuk mengetahui efek dari perbedaan dosis BMP-2 terhadap penyembuhan fraktur dengan defek tulang yang luas. Metode. Penelitian dilakukan di Laboratorium Animal Gizi di FKUI dan Laboratorium Patologi Anatomi FKUI-RSCM, pada bulan Juli hingga September 2015. Desain penelitian adalah randomized post test control group. Sejumlah 25 ekor tikus putih Sprague Dawley dengan usia 3-4 bulan dan berat badan antara 250 ? 350 gram, dibagi secara acak menjadi kelompok kontrol hidroksiapatit (HA) saja dan kelompok kombinasi HA + BMP-2 1 μg/ml, HA + BMP-2 5 μg/ml, HA + BMP-2 10 μg/ml, HA + BMP-2 20 µg/ml. Tiap kelompok dilakukan tindakan berupa frakturisasi dengan defek tulang 10mm pada femur kanan dan dilakukan fiksasi interna dengan menggunakan intramedullary k-wire ukuran 1,4 mm secara retrograd. Setelah 6 minggu dilakukan penilaian secara histomorfometri, radiologis dan Scanning Electron Microscope (SEM). Hasil. Berdasarkan hasil penelitian secara histomorfometri ditemukan terdapat perbedaan rerata total area kalus yang bermakna diantara kelompok penelitian (p<0,001),terdapat perbedaan bermakna rerata area penulangan antara kelompok kontrol dengan kelompok 1 μg/ml, 5 μg/ml, 10 μg/ml, 20 μg/ml (masing-masing p=0,009, p=0,016, p=0,009 dan p=0,016), terdapat perbedaan bermakna rerata area kartilago antara kelompok kontrol dengan kelompok 1 μg/ml, 5 μg/ml, 10 μg/ml, 20 μg/ml (masing-masing p=0,009, p=0,009, p=0,009 dan p=0,028), terdapat perbedaan bermakna rerata area fibrosis antara kelompok kontrol dengan kelompok 1 μg/ml dengan kelompok kontrol dan 10 μg/ml(masing-masing p=0,047 dan p=0,009).Secara radiologis dengan RUST score didapatkan perbedaan bermakna antara kelompok kontrol dengan kelompok 1 μg/ml, 5 μg/ml, 10 μg/ml, 20 μg/ml (masing-masing p=0,005, p=0,006, p=0,005 dan p=0,006). Dengan SEM didapatkan gambaran kalus yang lebih homogen dan padat pada kelompok 10μg/ml dibandingkan dengan 5 μg/ml dan 20 μg/ml. Kesimpulan: Pemberian BMP-2 dapat menstimulasi proses penyembuhan fraktur pada defek tulang luas (critical bone defect) yang bermakna secara statistik, histomorfometri, radiologis maupun secara kualitatif dengan SEM. Terdapat dosis optimal dalam pemberian BMP-2.ABSTRACT Introduction: Difficulties in the management of extensive bone defects is one of today's challenges. It is not only complex treatment but also can provide long-term negative severe effects. The use of BMP-2 in the treatment of fractures with extensive bone defect plays an important role. BMP-2 plays a role in the process of osteogenesis and chondrogenesis and inhibits osteoclastogenesis via the RANKL signaling. This study aims to determine the effect of differences in doses of BMP-2 on the healing of the fracture with extensive bone defects. Methods: The study was conducted at the Laboratory of Animal Nutrition at the Faculty of Medicine University of Indonesia (FMUI) in July until September 2015. The study design was randomized posttest control group. A number of 25 Sprague Dawley rats aged 3-4 months and bodyweight between 250-350 grams, were randomly divided into a control group of hydroxyapatite (HA) alone and HA+BMP-2 1 µg / ml, HA+BMP -2 5 ug / ml, HA + BMP-2 10 µg / ml, HA + BMP-2 20 ug / ml. Each group carried out fracturization with 10mm bone defect in right femur and internal fixation by using intramedullary K-wire size of 1.4 mm retrograde. After 6 weeks we did histomorfometri assessment, radiological and Scanning Electron Microscope (SEM). Results: Based on the research results histomorfometrcally found there are differences in the mean total area of ​​callus significantly between the study group (p <0.001), there were significant differences in the mean area of ​​woven bone between the control group with group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 ug / ml (respectively p = 0.009, p = 0.016, p = 0.009 and p = 0.016), there were significant differences in the average area of ​​the cartilage between the control group with group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 ug / ml (respectively p = 0.009, p = 0.009, p = 0.009 and p = 0.028), there were significant differences in the average area of ​​fibrosis between the control group with group 1 ug / ml in the control group and 10 mg / ml (respectively -masing p = 0.047 and p = 0.009) .In radiologist assessment with RUST scores obtained significant differences between the control group and group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 µg / ml (respectively p = 0.005 , p = 0.006, p = 0.005 and p = 0.006). SEM features with callus more homogeneous and dense in the group of 10μg / mL compared with 5 ug / ml and 20 µg / ml. Conclusion: Administration of BMP-2 could stimulate the process of fracture healing in large bone defects (critical bone defect) which was statistically significant with histomorfometri assestment, radiological and qualitatively with the SEM. There is an optimal dose in the administration of BMP-2.;Introduction: Difficulties in the management of extensive bone defects is one of today's challenges. It is not only complex treatment but also can provide long-term negative severe effects. The use of BMP-2 in the treatment of fractures with extensive bone defect plays an important role. BMP-2 plays a role in the process of osteogenesis and chondrogenesis and inhibits osteoclastogenesis via the RANKL signaling. This study aims to determine the effect of differences in doses of BMP-2 on the healing of the fracture with extensive bone defects. Methods: The study was conducted at the Laboratory of Animal Nutrition at the Faculty of Medicine University of Indonesia (FMUI) in July until September 2015. The study design was randomized posttest control group. A number of 25 Sprague Dawley rats aged 3-4 months and bodyweight between 250-350 grams, were randomly divided into a control group of hydroxyapatite (HA) alone and HA+BMP-2 1 µg / ml, HA+BMP -2 5 ug / ml, HA + BMP-2 10 µg / ml, HA + BMP-2 20 ug / ml. Each group carried out fracturization with 10mm bone defect in right femur and internal fixation by using intramedullary K-wire size of 1.4 mm retrograde. After 6 weeks we did histomorfometri assessment, radiological and Scanning Electron Microscope (SEM). Results: Based on the research results histomorfometrcally found there are differences in the mean total area of ​​callus significantly between the study group (p <0.001), there were significant differences in the mean area of ​​woven bone between the control group with group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 ug / ml (respectively p = 0.009, p = 0.016, p = 0.009 and p = 0.016), there were significant differences in the average area of ​​the cartilage between the control group with group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 ug / ml (respectively p = 0.009, p = 0.009, p = 0.009 and p = 0.028), there were significant differences in the average area of ​​fibrosis between the control group with group 1 ug / ml in the control group and 10 mg / ml (respectively -masing p = 0.047 and p = 0.009) .In radiologist assessment with RUST scores obtained significant differences between the control group and group 1 ug / ml, 5 µg / ml, 10 µg / ml, 20 µg / ml (respectively p = 0.005 , p = 0.006, p = 0.005 and p = 0.006). SEM features with callus more homogeneous and dense in the group of 10μg / mL compared with 5 ug / ml and 20 µg / ml. Conclusion: Administration of BMP-2 could stimulate the process of fracture healing in large bone defects (critical bone defect) which was statistically significant with histomorfometri assestment, radiological and qualitatively with the SEM. There is an optimal dose in the administration of BMP-2."

"[ABSTRAKLatar Belakang: Kebutuhan bahan pengganti tulang pada bidang bedah mulut dan maksilofasial semakin meningkat. Metode guided bone regeneration (GBR) yaitu suatu metode penambahan volume tulang dengan memungkinkan terjadinya pertumbuhan jaringan tulang yang selektif dalam suatu ruang, dimana pertumbuhan sel-sel tulang tersebut dijaga oleh suatu bahan (membran). Berkembangnya bahan biokomposit yang diketahui secara fakta bahwa pada penggunaan satu bahan saja tidak dapat digunakan untuk memenuhi seluruh kebutuhan pada penggunaan bahan implan pada biomedikal. Pada penelitian ini dibuat suatu komposit membran yang terdiri dari perpaduan bahan polivinilalkohol (PVA) + kolagen + hidroksiapatit. Kompositmembran (PVA-Kolagen-HA) diaplikasikan pada defek mandibular tikus Sprague-Dawley. Tujuan: Mengkaji penggunaan komposit membran (PVA-Kolagen- Hidroksiapatit) dalam regenerasi defek tulang mandibula pada hewan coba tikus perlakuan dibandingkan dengan hewan coba tikus kontrol dengan menilai sel osteoblas, sel radang dan angiogenesis.Metode Penelitian: 40 ekor tikus jantan jenis Sprague-Dawley usia 8-10 minggu dengan berat badan rata-rata 225 ± 25 gram. Tikus dibagi atas kelompok kontrol dan kelompok perlakuan dengan masing-masing berjumlah 20 ekor tikus. Dilakukan pembuatan defek pada angulus mandibular kiri tikus. Pada tikus kontrol tidak diaplikasi dengan komposit membran sedangkan pada kelompok perlakuan diaplikasi dengan komposit membran (PVA-Kolagen-HA). Kelompok kontrol dan kelompok perlakuan dengan komposit membran diamati sel osteoblas, sel radang dan angiogenesis melalui preparat histopatologi pada interval waktu hari ke-3, hari ke-7, hari ke-10, hari ke-14 dan hari ke-21. Hasil: Terdapat perbedaan bermakna (p<0,01) terhadap jumlah sel osteoblas, jumlah sel radang dan angiogenesis antara kelompok kontrol dan kelompok perlakuan dengan komposit membran (PVA-Kolagen-Hidroksiapatit). Terdapat perbedaan bermakna (p<0,01) antara jumlah sel osteoblas, jumlah sel radang dan angiogenesis terhadap interval waktu (3 hari, 7 hari, 10 hari, 14 hari dan 21 hari). Kesimpulan: Penggunaan komposit membran (PVA-Kolagen-Hidroksiapatit) mempercepat regenerasi tulang mandibular pada hewan coba tikus Sprague?Dawley.

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ABSTRACTBackground: The need of alternative bone substance in oral and maxillofacial surgery has increased. Guided bone regeneration method (GBR) is one of bone adding volume method by making the bone tissue regeneration to occur selectively in a room where the growth of bone cells are protected by a particular substance (membrane). It has been known that the developing biocomposite substance is cannot be achieved from only a single substance to recover all the requirements needed in the use of biomedic implant. In this study, a composite membrane consist of combination of polivinilalcohol material (PVA) + collagen + hydroxyapatite was made. Composite membrane applied on the mandibular defect of Sprague-Dawley rats.Objective: To evaluate the use of compocite membrane (PVA-Collagen-Hydroxyapatite) for regeneration of mandibular defect in animal testing (rats) comparing with group control of animal testing by observing the osteoblas, membrane (PVA-Collagen-HA) applied only in rats of testing group. The appearance of osteoblasts, inflammation cells, and angiogenesis were evaluated histopathologically on interval of 3rd, 7th, 10th, 14th and 21st day after application of composite membrane. Result: There are significant differences (p<0,01) in the number of osteoblast cells, inflammation cells and angiogenesis between the control group and the group applied with composite membrane (PVA-Collagen-Hydroxyapatite) on interval of determined days (day 3, day 7, day 10, day 14 and day 21st). Conclusion: Use of composite membrane (PVA-Collagen-Hydroxy) accelerates the mandibular bone regeneration of animal testing Sprague-Dawley rats.;Background: The need of alternative bone substance in oral and maxillofacial surgery has increased. There are many ways can be done to add bone volume.Guided bone regeneration method (GBR) is one of bone adding volume method bymaking the bone tissue regeneration to occur selectively in a room where thegrowth of bone cells are protected by a particular substance (membrane). It hasbeen known that the developing biocomposite substance is cannot be achieved fromonly a single substance to recover all the requirements needed in the use ofbiomedic implant. In this study, a composite membrane consist of combination ofpolivinilalcohol material (PVA) + collagen + hydroxyapatite was made. Compositemembrane applied on the mandibular defect of Sprague-Dawley rats.Objective: To evaluate the use of compocite membrane (PVA-CollagenHydroxyapatite)for regeneration of mandibular defect in animal testing (rats)comparing with group control of animal testing by observing the osteoblas,inflammation cells and angiogenesis.Method: 40 male Sprague-Dawley rats aged 8-10 months with weight ofapproximately 225 ± 25 grams were divided into two groups. First twenty rats weretreated as control group and another twenty rats for testing group. Defecation onleft angulus mandibula was done for all groups and composite membrane (PVACollagen-HA)appliedonlyinratsoftestinggroup.Theappearanceofosteoblasts,inflammationcells,andangiogenesiswereevaluatedhistopathologicallyonintervalof3rd,7th,10th,14thand21stdayafterapplicationofcompositemembrane.Thisstudywasdoneundercertificationfromtheresearchethicalcommittee.Result:Therearesignificantdifferences(p<0,01)inthenumberofosteoblastcells,inflammationcells and angiogenesis between the control group and the groupapplied with composite membrane (PVA-Collagen-Hydroxyapatite) on interval ofdetermined days (day 3, day 7, day 10, day 14 and day 21st).Conclusion: Use of composite membrane (PVA-Collagen-Hydroxy) accelerates the mandibular bone regeneration of animal testing Sprague-Dawley rats. ;Background: The need of alternative bone substance in oral and maxillofacial surgery has increased. There are many ways can be done to add bone volume.Guided bone regeneration method (GBR) is one of bone adding volume method bymaking the bone tissue regeneration to occur selectively in a room where thegrowth of bone cells are protected by a particular substance (membrane). It hasbeen known that the developing biocomposite substance is cannot be achieved fromonly a single substance to recover all the requirements needed in the use ofbiomedic implant. In this study, a composite membrane consist of combination ofpolivinilalcohol material (PVA) + collagen + hydroxyapatite was made. Compositemembrane applied on the mandibular defect of Sprague-Dawley rats.Objective: To evaluate the use of compocite membrane (PVA-CollagenHydroxyapatite)for regeneration of mandibular defect in animal testing (rats)comparing with group control of animal testing by observing the osteoblas,inflammation cells and angiogenesis.Method: 40 male Sprague-Dawley rats aged 8-10 months with weight ofapproximately 225 ± 25 grams were divided into two groups. First twenty rats weretreated as control group and another twenty rats for testing group. Defecation onleft angulus mandibula was done for all groups and composite membrane (PVACollagen-HA)appliedonlyinratsoftestinggroup.Theappearanceofosteoblasts,inflammationcells,andangiogenesiswereevaluatedhistopathologicallyonintervalof3rd,7th,10th,14thand21stdayafterapplicationofcompositemembrane.Thisstudywasdoneundercertificationfromtheresearchethicalcommittee.Result:Therearesignificantdifferences(p<0,01)inthenumberofosteoblastcells,inflammationcells and angiogenesis between the control group and the groupapplied with composite membrane (PVA-Collagen-Hydroxyapatite) on interval ofdetermined days (day 3, day 7, day 10, day 14 and day 21st).Conclusion: Use of composite membrane (PVA-Collagen-Hydroxy) accelerates the mandibular bone regeneration of animal testing Sprague-Dawley rats. , Background: The need of alternative bone substance in oral and maxillofacial surgery has increased. There are many ways can be done to add bone volume.Guided bone regeneration method (GBR) is one of bone adding volume method bymaking the bone tissue regeneration to occur selectively in a room where thegrowth of bone cells are protected by a particular substance (membrane). It hasbeen known that the developing biocomposite substance is cannot be achieved fromonly a single substance to recover all the requirements needed in the use ofbiomedic implant. In this study, a composite membrane consist of combination ofpolivinilalcohol material (PVA) + collagen + hydroxyapatite was made. Compositemembrane applied on the mandibular defect of Sprague-Dawley rats.Objective: To evaluate the use of compocite membrane (PVA-CollagenHydroxyapatite)for regeneration of mandibular defect in animal testing (rats)comparing with group control of animal testing by observing the osteoblas,inflammation cells and angiogenesis.Method: 40 male Sprague-Dawley rats aged 8-10 months with weight ofapproximately 225 ± 25 grams were divided into two groups. First twenty rats weretreated as control group and another twenty rats for testing group. Defecation onleft angulus mandibula was done for all groups and composite membrane (PVACollagen-HA)appliedonlyinratsoftestinggroup.Theappearanceofosteoblasts,inflammationcells,andangiogenesiswereevaluatedhistopathologicallyonintervalof3rd,7th,10th,14thand21stdayafterapplicationofcompositemembrane.Thisstudywasdoneundercertificationfromtheresearchethicalcommittee.Result:Therearesignificantdifferences(p<0,01)inthenumberofosteoblastcells,inflammationcells and angiogenesis between the control group and the groupapplied with composite membrane (PVA-Collagen-Hydroxyapatite) on interval ofdetermined days (day 3, day 7, day 10, day 14 and day 21st).Conclusion: Use of composite membrane (PVA-Collagen-Hydroxy) accelerates the mandibular bone regeneration of animal testing Sprague-Dawley rats. ]"

"Pendahuluan: Defek tulang kritis merupakan masalah yang menantang bagi ahli bedah ortopedi. Hingga saat ini, belum terdapat konsensus mengenai perlakuan tatalaksana terbaik untuk defek tulang kritis. Di antara berbagai solusi yang diusulkan, recombinant human bone morphogenetic protein-2 (rhBMP-2) adalah osteoinduktor yang paling poten, dan telah menunjukkan hasil yang menjanjikan. Penelitian sebelumnya seringkali menggunakan rhBMP-2 yang didapatkan dari sel ovarium hamster Cina. Namun, rhBMP- 2 yang didapatkan dari sel ovarium hamster Cina ini memiliki berbagai kekurangan seperti biaya tinggi dan hasil produksi yang rendah. Baru-baru ini, rhBMP-2 yang berasal dari Escherichia coli semakin banyak digunakan karena hasil panen yang tinggi dan biaya yang rendah; namun, protein tersebut diekspresikan sebagai badan inklusi, yang memerlukan pemrosesan ekstensif untuk menghasilkan protein bioaktif. Untuk mengatasi kendala-kendala ini, diperlukan metode produksi rhBMP-2 yang efisien. Sampai saat ini, belum terdapat penelitian yang mengevaluasi penggunaan vektor adenovirus untuk transfer gen rhBMP-2 ke sel punca mesenkimal asal jaringan adiposa (SPM-AD) pada model defek tulang kritis pada tikus Sprague-Dawley. Penelitian ini adalah studi eksperimental yang mengevaluasi efektivitas rhBMP-2 yang berasal dari SPM-AD yang direkayasa secara genetik pada model defek tulang kritis pada tikus Sprague-Dawley.Metode: Penelitian ini menggunakan tikus Sprague Dawley sebanyak 36 ekor. Dibuat cacat tulang berdiameter 5 mm terjadi pada diafisis femur pada setiap tikus. Hewan- hewan tersebut dibagi menjadi empat kelompok yang masing-masing kelompok terdiri dari 9 ekor tikus. Kelompok pertama mendapatkan rhBMP-2 yang berasal dari SPM-AD yang dimodifikasi secara genetik dengan granul hidroksiapatit (HA) (kelompok rhBMP- 2), kelompok kedua mendapatkan sekretom SPM-AD dan granul HA (kelompok sekretom AD-MSC), kelompok ketiga mendapatkan granul HA (kelompok HA), dan yang keempat adalah kelompok kontrol. Adenovirus digunakan sebagai vektor transfer gen untuk mentransduksi rhBMP-2 ke SPM-AD. Larutan akhir yang digunakan dalam penelitian ini terdiri dari campuran lisat dan sekretom SPM-AD dengan perbandingan 2:1, dan konsentrasi akhir rhBMP-2 adalah 132,33 pg/mL. Tikus dikorbankan 8 minggu setelah operasi. Tulang femur dipanen dan diperiksa nilai protein Indian hedgehog (Ihh), parameter histomorfometri, dan load to failure.Hasil dan Pembahasan: Selama periode pengamatan, masing-masing terdapat satu, dua, dan dua ekor tikus mati pada kelompok rhBMP-2, HA, dan kontrol. Kelompok rhBMP-2 memiliki protein Ihh lebih tinggi dibandingkan kelompok HA dan kontrol. Kelompok rhBMP-2 juga memiliki total area kalus dan nilai load to failure yang lebih tinggi dibandingkan ketiga kelompok lainnya. Proses penyembuhan yang unggul dari kelompok rhBMP-2 kemungkinan dihasilkan dari sifat rhBMP-2 itu sendiri yang mendorong diferensiasi sel punca mensenkimal menjadi osteoblas, sehingga menghasilkan regenerasi tulang.Kesimpulan: Hasil penelitian ini menunjukkan bahwa penggunaan rhBMP-2 yang berasal dari SPM-AD yang dimodifikasi secara genetik berhasil menatalaksana defek tulang kritis pada tikus Sprague-Dawley.

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Introduction: Critical-sized bone defects (CSBDs) remain challenging problem for orthopaedic surgeons. To date, there are no consensus regarding the best treatment for such entity.

Among various solutions proposed, recombinant human bone morphogenetic

protein-2 (rhBMP-2) is the most potent osteoinductor, and it has shown promising results. Early orthopaedic studies used mammalian cell-derived rhBMP-2, especially Chinese hamster ovary (CHO) cells. However, CHO cell-derived rhBMP-2 presents disadvantages such as high cost and low production yield. Recently, Escherichia coli- derived rhBMP-2 has been increasingly used owing to the high yield and low cost; however, the protein is expressed as inclusion bodies, which need extensive processing involving isolation from cell, solubilization, refolding and purification to produce the bioactive proteins. To overcome these obstacles, an efficient method for producing rhBMP-2 is required. To date, there is no study that has evaluated the use of adenovirus vector for gene transfer of rhBMP-2 to adipose-derived mesenchymal stem cells (AD-

MSCs)

in CSBDs model in Sprague-Dawley rats. This is an experimental study that evaluated the efficacy of rhBMP-2 derived from genetically-modified AD-MSCs in CSBDs model in Sprague-Dawley rats.

Methods: A total of 36 Sprague Dawley rats were examined in this study. A bone defect of 5 mm in diameter was created in femoral diaphysis in each of the rat. The animals were divided into four groups of 9 rats each. The first group received rhBMP-2 derived from genetically-modified AD-MSCs with hydroxyapatite (HA) granules (rhBMP-2 group), the second received AD-MSCs secretome and HA granules (AD-MSCs secretome group), the third received HA granules (HA group), and the fourth was control group. Adenoviruses were used as gene transfer vectors to transduce rhBMP-2 to AD-MSCs. The final solution consisted of AD-MSCs lysate and their secretome with ratio of 2:1, and the concentration of rhBMP-2 was 132.33 pg/mL. The rats were sacrificed 8 weeks after the surgery. The femurs were harvested and submitted for Indian hedgehog (Ihh) protein, histomorphometric parameters, and load to failure analyses.

Results and Discussion: During the observation period, one, two, and two rats died in the rhBMP-2, HA, and control groups, respectively. The rhBMP-2 group had higher Ihh protein compared to HA and control groups. The rhBMP-2 group also had higher callus total area, and load to failure value compared to the other three groups. The superior healing process from the rhBMP-2 group might be due to the property of rhBMP-2 itself which promotes differentiation of mesenchymal stem cells into osteoblasts, resulting in bone regeneration.

Conclusion: The results of this study indicate that the use of rhBMP-2 derived from genetically-modified AD-MSCs could successfully treat CSBDs in Sprague-Dawley rats."

"Pendahuluan: Defek tulang kritis adalah hilangnya struktur tulang yang melebihi ukuran kritis kemampuan tulang untuk beregenerasi. Pencangkokan tulang autologus sebagai terapi standar diperlukan pada defek tulang yang luas. Namun, hal ini dikaitkan dengan berbagai morbiditas. Penggunaan eksosom dari sel punca mesenkimal tali pusat (SPM- TP) dan PRF cukup menjanjikan dan berpotensi menjadi alternatif untuk mencapai penyembuhan defek tulang kritis.Metode: Penelitian ini merupakan penelitian eksperimental post-test only control group design dengan menggunakan 30 ekor tikus Sprague Dawley yang berusia 8-12 minggu dengan berat badan sekitar 250-300 gram. Tikus-tikus tersebut kemudian dibagi menjadi 5 kelompok perlakuan, yaitu hidroksiapatit (HA) dan cangkok tulang (kelompok I), HA, cangkok tulang, dan PRF (kelompok II), HA, cangkok tulang, dan eksosom dari UC-MSC (kelompok III), HA, cangkok tulang, PRF, dan eksosom dari UC-MSC (kelompok IV), serta HA, PRF, dan eksosom dari UC-MSC (kelompok V). Pada setiap tikus, defek tulang femur 5mm dibuat dan difiksasi secara internal menggunakan ulir kawat K 1,0-1,2 mm. Pada minggu keempat masa tindak lanjut, pemeriksaan RT-PCR dilakukan untuk menilai kadar BMP-2 dan chordin, serta pemeriksaan histomorfometri untuk mengukur persentase area osifikasi, area fibrosis, dan area void. Analisis statistik dilakukan dengan menggunakan uji ANOVA satu arah dan uji post-hoc untuk menentukan signifikansi hasil.Hasil: Pada pemeriksaan RT-PCR, ekspresi gen BMP-2 tertinggi ditemukan pada kelompok I (1,0 - 1,5; median 1,2), diikuti oleh kelompok II (0,2 - 1,2; median 0,5), kelompok IV (0,3 - 0,7; median 0,4), kelompok III dan kelompok V. Sementara itu, ekspresi gen chordin tertinggi terdapat pada kelompok III (0 - 50), diikuti oleh kelompok lainnya dengan nilai yang sama. Namun, analisis deskriptif menunjukkan tidak ada korelasi yang signifikan antara tingkat BMP-2 dan chordin pada defek tulang kritis, dengan nilai p masing-masing 0,096 dan 0,690. Analisis statistik menunjukkan hasil yang signifikan untuk BMP-2 (p = 0,017) sementara chordin (p = 0,269) dan analisis histomorfometri untuk area osifikasi, fibrosis, dan inflamasi kronis (jaringan granulasi), dan area kosong tidak menunjukkan signifikansi statistik (p = 0,591, p = 0,581, p = 0,196).Diskusi: Penggunaan PRF dan eksosom dari SPM-TP secara terpisah menunjukkan hasil yang berbeda, dimana PRF menunjukan hasil yang baik pada osteogenesis daneksosom dari SPM-TP menunjukan hasil lebih tinggi dalam pembentukan jaringan fibrosis, dan inflamasi kronis (jaringan granulasi). Pada beberapa penelitian, PRF terbukti meningkatkan kadar BMP-2 dan diferensiasi osteoblas, sehingga mempercepat proses osteogenesis. Namun, penggunaan eksosom dan PRF secara bersamaan belum diteliti pengaruhnya terhadap defek tulang kritis. Dalam penelitian ini, hasil yang berlawanan ditemukan daripada hasil yang diharapkan, dengan kadar BMP-2 yang relatif rendah pada kelompok perlakuan kombinasi dibandingkan dengan kelompok lain, dan adanya peningkatan kadar chordin pada kelompok perlakuan kombinasi. Hal ini menunjukkan bahwa kombinasi PRF dan eksosom dari SPM-TP dapat menghasilkan efek negatif pada osteogenesis.Kesimpulan: Secara terpisah, PRF telah terbukti memiliki efek positif pada osteogenesis, sedangkan eksosom dari SPM-TP menunjukan hasil lebih tinggi dalam pembentukan jaringan fibrosis, dan inflamasi kronis (jaringan granulasi). Kombinasi keduanya dalam penelitian ini, tidak memberikan efek positif terhadap regenerasi defek tulang kritis.

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Introduction: Critical bone defect is a loss of bone structure that exceeds the critical size of the bone's ability to regenerate. Autologous bone grafting as the standard therapy is needed in extensive bone defects. However, it is associated with various morbidities. The use of exosome from umbilical cord mesenchymal stem cell (UC-MSC) and PRF is promising and has the potential to be an alternative to achieve healing of critical bone defects.

Methods: This study was an experimental post-test only control group design using 30 Sprague Dawley rats aged 8-12 weeks, weighing about 250-300 grams. They were then divided into 5 treatment groups, namely hydroxyapatite (HA) and bone graft (group I), HA, bone graft, and PRF (group II), HA, bone graft and exosome from UC-MSC (group III), HA, bone graft, PRF, and exosome from UC-MSC (group IV), and HA, PRF, and exosome from UC-MSC (group V). In each rat, a 5mm femoral bone defect was created and internally fixated using a 1.0-1.2 mm K-wire threaded. At the fourth week of follow- up, RT-PCR examination was performed to assess BMP-2 and chordin levels, as well as histomorphometry examination to measure the percentages of ossification area, fibrotic area, and void area. Statistical analysis was conducted using one-way ANOVA and post- hoc tests to determine the significance of the results.

Results: In the RT-PCR examination, the highest BMP-2 gene expression was found in group I (1.0 - 1.5; median 1.2), followed by group II (0.2 - 1.2; median 0.5), group IV (0.3 - 0.7; median 0.4), group III and group V. Meanwhile, chordin gene expression was highest in group III (0 - 50), followed by the other groups with similar values. However, descriptive analysis showed no significant correlation between BMP-2 and chordin levels in critical bone defects, with p values of 0.096 and 0.690 each. Statistical analysis showed significant results for BMP-2 (p = 0.017) while chordin (p = 0.269) and histomorphometry analysis for ossification, fibrotic, and void area showed no statistical significance (p = 0.591, p = 0.581, p = 0.196, respectively).

Discussion: The use of PRF and exosomes from SPM-TP separately showed different results, where PRF showed good results in osteogenesis and exosomes from SPM-TP showed higher results in fibritic tissue formation. However, the use of both exosomes and PRF together has not been studied for their effect on critical bone defects. In this study, the opposite results were found instead of the expected results. This may indicate that the combination of PRF and exosome from UC-MSC could possibly yield a negative effect on osteogenesis.

Conclusion: The combination of PRF and exosome from UC-MSC did not yield positive effect on the outcomes examined in this study."

"ABSTRAKLatar belakang: Cidera saraf perifer sebagai keluaran dari post operatif hingga saat ini belum ditangani dengan maksimal. Penelitian ini ditujukan untuk menentukan potensi dari sekretom pada regenerasi cidera saraf perifer.Metode: Cidera saraf perifer buatan dilakukan pada tikus dengan melakukan diseksi pada saraf sciatic. Evaluasi perbaikan motorik dilakukan mengunakan Sciatic Functional Index (SFI) pada minggu ke enam (SFI 1), minggu ke sembilan (SFI 2), dan minggu ke dua belas (SFI 3). Rasio berat basah antara otot gastrocnemius kanan dan kiri dibandingkan serta dilakukan histomorphometry saraf sciatic pada tiap kelompok.Hasil: Kelompok III menunjukan SFI 1 yang lebih baik dibandingkan kelompok I (p=0.017). Kelompok I dan III menunjukan perbedaan SF2 yang signifikan dibandingkan dengan kelompok II dan IV (p<0.001). Rasio tertinggi dari otot gastrocnemius ditemukan pada kelompok I dan III, yang bernilai 0.65 ± 0.059 dan 0.67 ± 0.179 (p<0.001). Pada histomorphometry, akson termyelinisasi paling banyak ditemukan pada kelompok I dan III, yang bernilai p<0.001.Kesimpulan: Sekretom sel punca mesenkimal korda umbilikalis dapat digunakan sebagai terapi baru untuk menggantikan autograf pada penanganan kerusakan saraf perifer.

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ABSTRACTBackground: Currently, the post-surgical outcome of peripheral nerve injury has not been optimal. The purpose of this research is to determine the potency of secretome in peripheral nerve injury regeneration.Method: The mice had artificially-induced peripheral nerve injury, which was created by dissecting the sciatic nerve. Sciatic Functional Index (SFI) was used to evaluate the motoric recovery on week six (SFI 1), week nine (SFI 2), and week twelve (SFI 3). The mice was sacrificed on week twelve. The wet mass ratios of the right and left gastrocnemius muscle were compared, then the sciatic nerve histomorphometry evaluation was performed on each group.Results: Group III showed a better SFI 1 result than Group I (p=0.017). Group I and III showed significantly better SFI 2 than group II and IV (p<0.001). The highest ratio of gastrocnemius muscle was found in group I and III, which were 0.65 ± 0.059 and 0.67 ± 0.179 (p<0.001). On histomorphometry, the highest number of myelinated axons were found in group I and III, which were p<0.001.Conclusion: Umbilical cord mesenchymal stem cell secretome can be used as a new therapy to replace the autograft in peripheral nerve defect management."