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内皮细胞在小鼠卵黄囊干细胞分化调控中的作用。

Role of endothelium in the control of mouse yolk sac stem cell differentiation.

作者信息

Auerbach R, Wang S J, Yu D, Gilligan B, Lu L S

机构信息

Laboratory of Developmental Biology, University of Wisconsin, Madison 53706, USA.

出版信息

Dev Comp Immunol. 1998 May-Jun;22(3):333-8. doi: 10.1016/s0145-305x(98)00005-6.

Abstract

Studies in our laboratory have shown that as early as day 8.5 of development, mouse yolk sac cells can generate T cells when placed in a thymic microenvironment. At this stage, yolk sac cells can also differentiate into myeloid cells in vitro. B cell differentiation in vitro was achieved with day 9 yolk sac by providing a bone marrow stromal feeder layer. We have now established endothelial cell lines and clones from yolk sacs of day 8-12 mouse embryos. These vary in their ability to support stem cell maintenance and differentiation. Our principal work has been carried out with day 12 cloned endothelial cell lines. One clone supported the > 100 fold expansion of yolk sac hematopoietic stem cells that subsequently could generate B cells, T cells and myeloid cells both in vitro and in vivo. Preliminary experiments with endothelial cells from younger embryos are also described.

摘要

我们实验室的研究表明,早在发育的第8.5天,小鼠卵黄囊细胞置于胸腺微环境中时就能产生T细胞。在此阶段,卵黄囊细胞在体外也能分化为髓系细胞。通过提供骨髓基质饲养层,第9天的卵黄囊在体外实现了B细胞分化。我们现已从小鼠胚胎第8 - 12天的卵黄囊中建立了内皮细胞系和克隆。它们在支持干细胞维持和分化的能力上有所不同。我们的主要工作是用第12天的克隆内皮细胞系进行的。其中一个克隆支持卵黄囊造血干细胞扩增100倍以上,随后这些干细胞在体外和体内都能产生B细胞、T细胞和髓系细胞。文中还描述了用较早期胚胎的内皮细胞进行的初步实验。

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