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在没有添加生长因子的情况下,细胞凋亡的抑制可使多能造血细胞系实现分化和发育。

Suppression of apoptosis allows differentiation and development of a multipotent hemopoietic cell line in the absence of added growth factors.

作者信息

Fairbairn L J, Cowling G J, Reipert B M, Dexter T M

机构信息

Cancer Research Campaign Department of Experimental Haematology, Paterson Institute for Cancer Research, Christie Hospital, Manchester, England.

出版信息

Cell. 1993 Sep 10;74(5):823-32. doi: 10.1016/0092-8674(93)90462-y.

Abstract

In the absence of growth factors, hemopoietic cells die rapidly by the process of apoptosis. Transfection of the human bcl-2 gene into an interleukin-3 (IL-3)-dependent, multipotent hemopoietic cell line allowed these cells to survive in the absence of IL-3, both in serum-containing and serum-deprived conditions, and this survival was accompanied by multilineage differentiation. Moreover, single cell experiments showed that differentiation could occur in the absence of cell division. While these data do not rule out the possibility that growth factors can influence the lineage choice of multipotent cells, they suggest that exposure to growth factors may not be obligatory for the differentiation of stem cells. The data also support the hypothesis that differentiation is intrinsically determined and that the role of the hemopoietic growth factors is enabling rather than inductive.

摘要

在缺乏生长因子的情况下,造血细胞通过凋亡过程迅速死亡。将人类bcl-2基因转染到依赖白细胞介素-3(IL-3)的多能造血细胞系中,使这些细胞在含血清和无血清条件下均能在无IL-3的情况下存活,并且这种存活伴随着多谱系分化。此外,单细胞实验表明,分化可以在无细胞分裂的情况下发生。虽然这些数据并不排除生长因子可能影响多能细胞谱系选择的可能性,但它们表明,暴露于生长因子可能不是干细胞分化所必需的。这些数据还支持这样一种假说,即分化是内在决定的,造血生长因子的作用是促成而非诱导。

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