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Efficient expansion of mesenchymal stromal cells from umbilical cord under low serum conditions

机译:低血清条件下脐带间充质基质细胞的有效扩增

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摘要

Background aims Mesenchymal stromal cells (MSC) are of clinical interest for their potential use in regenerative medicine and immunotherapy. Originally derived from bone marrow (BM), MSC have now been isolated from most tissues, including umbilical cord (UC) and UC blood (UCB). If MSC from UC are biologically equivalent to those from BM, they would be attractive as a readily available and non-invasive source for cellular therapies. Methods Sections of UC were separated into vascular and Wharton's jelly (WJ) fractions, which were then digested individually to release MSC that were isolated by plastic adherence in a 10% fetal calf serum (FCS) medium, or a low serum medium designed for multi-potent adult progenitor cells (MAPC). The resulting perivascular (PV) and WJ MSC lines were assayed for expression of characteristic markers and differentiation and immunosuppressive properties. Results MSC lines were readily derived from most UC tested. Cells grown in MAPC medium (MM) tended to be smaller and more elongated and expressed more nestin, but did not differ substantially in their growth rate, expression of other markers and differentiation capacity. All UC lines tested were adipogenic but poorly osteogenic, and were equivalent in their ability to suppress T-cell proliferation induced by phytohemagglutinin (PHA), activation beads and allostimulation. Conclusions UC is a convenient, efficient source of MSC that can be expanded under low serum conditions for application on future studies of tissue regeneration and immunosuppression.
机译:背景目的间充质基质细胞(MSC)在再生医学和免疫疗法中的潜在用途具有临床意义。 MSC最初源自骨髓(BM),现已从大多数组织中分离出来,包括脐带(UC)和UC血液(UCB)。如果来自UC的MSC与来自BM的MSC在生物学上是等效的,它们作为一种容易获得且无创的细胞疗法来源将具有吸引力。方法将UC切片分为血管和沃顿胶质(WJ)馏分,然后分别消化以释放MSC,通过在10%胎牛血清(FCS)培养基或专为多胎牛血清设计的低血清培养基中进行塑料粘附分离潜能成年祖细胞(MAPC)。分析所得的血管周围(PV)和WJ MSC系的特征性标志物的表达以及分化和免疫抑制特性。结果MSC系很容易从大多数测试的UC中获得。在MAPC培养基(MM)中生长的细胞趋向于更小,更细长并且表达更多的巢蛋白,但在它们的生长速度,其他标记物的表达和分化能力上没有实质性差异。所有测试的UC系均具有成脂性,但成骨性差,并且在抑制植物血凝素(PHA),活化珠和同种异体刺激诱导的T细胞增殖方面具有同等的能力。结论UC是一种方便,有效的MSC来源,可在低血清条件下扩增,用于将来的组织再生和免疫抑制研究。

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