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The isolation and in situ identification of MSCs residing in loose connective tissues using a niche-preserving organ culture system

机译:保留小生境的器官培养系统分离并原位鉴定散在结缔组织中的MSC

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摘要

Mesenchymal stem cells (MSCs) have been discovered in a multitude of organs, but their distribution and identity are still uncertain Furthermore, loose connective tissue (LCT) is dispersed throughout virtually all organs, but its biological role in tissue homeostasis is unclear Here, we describe a unique organ culture system to explore the omnipresence and in situ identity of MSCs among the LCTs This culture system included the use of the fibrin hydrogel coupled with dynamic culture conditions, using native LCTs obtained from various organs as starting materials This culture allowed MSC outgrowth into the hydrogel to be robustly supported, while maintaining the structural integrity of LCTs during in vitro culture Subcultured outgrown cells fulfilled the minimal requirements for defining MSCs on the basis of clonogenicity, multipotency, and immunophenotypic characteristics In vitro label-retaining assay demonstrated that the numbers of mobilized and proliferated cells in situ increased in the pericapillary region and expressed both MSCs and pericytes markers, indicating that the in situ identity of MSCs represents a certain population of pericapillary pericytes Our results indicate that this culture system affords a unique strategy for both isolating MSCs and recapitulating their niche in LCTs
机译:间充质干细胞(MSCs)已在许多器官中发现,但其分布和身份仍不确定。此外,疏松结缔组织(LCT)几乎遍布所有器官,但其在组织稳态中的生物学作用尚不清楚。描述了一个独特的器官培养系统,以探索LCT中MSC的无处不在和原位身份。该培养系统包括使用纤维蛋白水凝胶以及动态培养条件,使用从各个器官获得的天然LCT作为起始材料。这种培养可以使MSC向外生长到水凝胶中以得到有力的支持,同时在体外培养过程中保持LCT的结构完整性。继代培养的生长细胞满足了基于克隆形成性,多能性和免疫表型特征定义MSC的最低要求。原位动员和增殖细胞的数量增加在毛细血管周围区域表达并表达了MSCs和周细胞标记,表明MSCs的原位身份代表了一定数量的毛细血管周细胞。我们的结果表明,该培养系统为分离MSCs和重现LCT中的生态位提供了独特的策略

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