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首页> 外文期刊>Current stem cell research & therapy >Amniotic Membrane Transplant for Articular Cartilage Repair: An Experimental Study in Sheep
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Amniotic Membrane Transplant for Articular Cartilage Repair: An Experimental Study in Sheep

机译:羊膜移植修复关节软骨:绵羊的实验研究

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摘要

Purpose: The aim of the present study was to compare the potential for cartilage repair of fresh amniotic membrane (AM), cryopreserved AM and cryopreserved AM previously cultured with bone marrow mesenchymal stem cells (BM-MSCs) in an in vivo sheep animal model. Methods: A full-thickness cartilage defect was surgically produced in 12 adult sheep, in the bearing region of the lateral femoral condyle. The animals were randomized into 4 groups (n=3): no treatment of the defect (G1); filling with fresh AM (G2); with cryopreserved AM previously cultivated with BM-MSCs (G3); with cryopreserved AM alone (G4). Postoperatively, the full load was possible. At two months, the animals were euthanized. The quality of the new synthesized tissue was evaluated with the macroscopic, by using International Cartilage Repair Society (ICRS) scale, and histological analyses, by using O'Driscoll scale. Results: The control samples showed an ICRS grade III (abnormal); while the samples of Groups 2, 3 and 4 reported a grade II (similar to healthy cartilage). The mean value of O'Driscoll scale in the control group (3.3) was significantly lower compared to the treatment groups (G2: 10.7; G3: 8; G4: 11.3) (P < 0.05). No significant differences were found between the experimental groups. Conclusion: AM could be a suitable material for the management of articular cartilage defects. Stem cells within AM demonstrated to be able to differentiate in chondrocytes in vivo. Fresh AM, cryopreserved AM and cryopreserved AM previously cultivated with BM-MSCs showed similar regenerative properties.
机译:目的:本研究的目的是在体内绵羊动物模型中比较先前用骨髓间充质干细胞(BM-MSC)培养的新鲜羊膜(AM),冷冻保存的AM和冷冻保存的AM的软骨修复潜力。方法:通过手术在12只成年绵羊的股骨外侧lateral承窝区域产生全厚度软骨缺损。将动物随机分为4组(n = 3):不治疗缺损(G1);装满新鲜的AM(G2);预先用BM-MSC(G3)培养的低温保存的AM;单独使用冷冻保存的AM(G4)。术后,全负荷是可能的。两个月后,对动物实施安乐死。使用国际软骨修复协会(ICRS)量表,通过宏观评估新合成组织的质量;使用O'Driscoll量表,进行组织学分析。结果:对照样品显示出ICRS III级(异常)。而第2、3和4组的样本报告为II级(类似于健康的软骨)。对照组的O'Driscoll量表的平均值(3.3)显着低于治疗组(G2:10.7; G3:8; G4:11.3)(P <0.05)。实验组之间没有发现显着差异。结论:AM可能是治疗关节软骨缺损的合适材料。 AM中的干细胞被证明能够在体内分化成软骨细胞。新鲜的AM,低温保存的AM和先前用BM-MSC培养的低温保存的AM显示出相似的再生特性。

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