首页> 美国卫生研究院文献>The Journal of Veterinary Medical Science >Independent chondrogenic potential of canine bone marrow-derived mesenchymal stem cells in monolayer expansion cultures decreases in a passage-dependent pattern
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Independent chondrogenic potential of canine bone marrow-derived mesenchymal stem cells in monolayer expansion cultures decreases in a passage-dependent pattern

机译:单层扩增培养物中犬骨髓间充质干细胞的独立成软骨潜力以传代依赖性方式降低

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摘要

Although chondroinductive growth factors are considered necessary for chondrogenesis of bone marrow-derived mesenchymal stem cells (BMSC), independent and spontaneous chondrogenesis has been previously demonstrated in adult horses, bovine calves and adult human BMSC. Surprisingly, adult canine BMSC under similar culture conditions previously failed to demonstrate chondrogenesis. The present study evaluated independent chondrogenic potential of BMSC sourced from three young dogs in the absence of known chondroinductive factors. BMSC were culture expanded in 10% DMEM up to third passage (P3). At each passage, the phenotype of BMSC was evaluated by RT-PCR gel electrophoresis and qPCR. BMSC exhibited a chondrogenic phenotype in the absence of dexamethasone and TGF-β1 as verified by the expression of Sox-9, type II collagen and aggrecan. Sox-9 was significantly downregulated (P<0.05) from P1−P3 compared to P0 while type II and X collagen, and aggrecan were significantly downregulated at P3 compared to P0. There was a significant (P<0.01) negative correlation between passaging and Sox-9, type II collagen and aggrecan gene expression. These results indicate that independent chondrogenic potential and phenotype retention of BMSC decreases in a passage-dependent pattern. Therefore, caution should be exercised for future experiments evaluating the chondrogenic potential of BMSC after extensive expansion cultures in 10% DMEM.
机译:尽管软骨诱导生长因子被认为是骨髓源性间充质干细胞(BMSC)软骨形成所必需的,但先前已在成年马,牛犊和成年人类BMSC中证明了独立和自发的软骨形成。令人惊讶的是,成年犬BMSC在相似的培养条件下以前未能证明软骨形成。本研究评估了在缺乏已知软骨诱导因子的情况下,来自三只幼犬的BMSC的独立软骨形成潜力。在10%DMEM中将BMSC培养扩增至第三代(P3)。在每次传代中,通过RT-PCR凝胶电泳和qPCR评估BMSC的表型。 BMSC在没有地塞米松和TGF-β1的情况下表现出软骨形成的表型,这一点已通过Sox-9,II型胶原和蛋白聚糖的表达得到证实。与P0相比,Sox-9从P1-P3显着下调(P <0.05),而II型和X型胶原和聚集蛋白聚糖在P3上与P0相比显着下调。传代与Sox-9,II型胶原和聚集蛋白聚糖基因表达之间存在显着(P <0.01)负相关。这些结果表明,BMSC的独立成软骨潜力和表型保留率以传代依赖性方式降低。因此,在10%DMEM中大量扩增培养后,评估未来BMSC软骨形成潜力的实验应谨慎行事。

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