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首页> 外文期刊>Biomaterials >The osteogenic differentiation of adult bone marrow and perinatal umbilical mesenchymal stem cells and matrix remodelling in three-dimensional collagen scaffolds.
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The osteogenic differentiation of adult bone marrow and perinatal umbilical mesenchymal stem cells and matrix remodelling in three-dimensional collagen scaffolds.

机译:成年骨髓和围产期脐带间充质干细胞的成骨分化和三维胶原蛋白支架的基质重塑。

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摘要

Adult human mesenchymal stem cells from bone marrow (BM-MSC) represent a promising source for skeletal regeneration. Perinatal MSC from Wharton's Jelly of the umbilical cord (UC-MSC) are expected to possess enhanced differentiation capacities due to partial expression of pluripotency markers. For bone tissue engineering, it is important to analyse in vitro behaviour of stem cell/biomaterial hybrids concerning in vivo integration into injured tissue via migration, matrix remodelling and differentiation. This study compares the cell-mediated remodelling of three-dimensional collagen I/III gels during osteogenic differentiation of both cell types. When activated through collagen contact and subjected to osteogenic differentiation, UC-MSC differ from BM-MSC in expression and synthesis of extracellular matrix (ECM) proteins as shown by histology, immunohistochemistry, Western Blot analysis and realtime-RT-PCR. The biosynthetic activity was accompanied in both cell types by the ultrastructural appearance of hydroxyapatite/calcium crystals and osteogenic gene induction. Following secretion of matrix metalloproteinases (MMP), both MSC types migrated into and colonised the collagenous matrix causing matrix strengthening and contraction. These results indicate that UC-MSC and BM-MSC display all features needed for effective bone fracture healing. The expression of ECM differs in both cell types considerably, suggesting different mechanisms for bone formation and significant impact for bone tissue engineering.
机译:来自骨髓的成人间充质干细胞(BM-MSC)代表了骨骼再生的有希望的来源。由于多能性标记物的部分表达,来自沃顿脐带果冻(UC-MSC)的围产期MSC有望具有增强的分化能力。对于骨组织工程,分析干细胞/生物材料杂种的体外行为与通过迁移,基质重塑和分化体内整合到受损组织中有关,这一点很重要。这项研究比较了两种细胞类型的成骨分化过程中三维胶原蛋白I / III凝胶的细胞介导重塑。当通过胶原蛋白接触激活并经历成骨分化时,UC-MSC与BM-MSC在细胞外基质(ECM)蛋白的表达和合成方面有所不同,如组织学,免疫组织化学,蛋白质印迹分析和实时RT-PCR所示。在两种细胞类型中,生物合成活性都伴随着羟基磷灰石/钙晶体的超微结构出现和成骨基因诱导。基质金属蛋白酶(MMP)分泌后,两种MSC类型都迁移到胶原基质中并在其中定殖,从而引起基质增强和收缩。这些结果表明,UC-MSC和BM-MSC具有有效的骨折愈合所需的所有功能。在两种细胞类型中,ECM的表达都存在显着差异,表明骨骼形成的机制不同,并且对骨骼组织工程的影响很大。

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