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胎儿和成人造血干细胞的层次组织。

Hierarchical organization of fetal and adult hematopoietic stem cells.

作者信息

Babovic Sonja, Eaves Connie J

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency and University of British Columbia, 675 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3.

Terry Fox Laboratory, British Columbia Cancer Agency and University of British Columbia, 675 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3.

出版信息

Exp Cell Res. 2014 Dec 10;329(2):185-91. doi: 10.1016/j.yexcr.2014.08.005. Epub 2014 Aug 13.

Abstract

Mammalian hematopoiesis is a hierarchically organized process in which all types of mature blood cells are continuously generated from more primitive cells that lack any morphological evidence of differentiation. However, it is now accepted that this morphologically homogeneous precursor population consists of multiple distinct subsets of cells. The most primitive of these are defined by their ability to produce similarly undifferentiated progeny through many cell divisions, in addition to generating cells with activated differentiation programs. The term hematopoietic stem cell (HSC) is now conventionally restricted to cells with this long-term self-sustaining ability. Nevertheless, clonal tracking studies have revealed significant heterogeneity in the behavior of such stringently defined HSCs. Moreover, superimposed on the heterogeneous behavior that can be elicited from the HSCs present at any given time during development are additional differences that distinguish HSCs at different times both before and after birth. The latter include changes in the representation of HSCs that display specific differentiation programs, as well as changes in their turnover and self-renewal control. Here, we summarize recent studies characterizing these developmental changes, some of the mechanisms that control them, and their potential relevance to understanding age-associated differences in leukemia as well as normal hematopoiesis.

摘要

哺乳动物造血是一个层次有序的过程,在此过程中,所有类型的成熟血细胞都由缺乏任何分化形态学证据的更原始细胞持续产生。然而,现在人们认识到,这个形态学上均一的前体细胞群体由多个不同的细胞亚群组成。其中最原始的细胞通过多次细胞分裂产生同样未分化的子代细胞,此外还能产生具有激活分化程序的细胞,以此来定义。造血干细胞(HSC)这个术语现在通常局限于具有这种长期自我维持能力的细胞。然而,克隆追踪研究揭示了这类严格定义的造血干细胞行为存在显著异质性。此外,在发育过程中任何给定时间存在的造血干细胞所引发的异质性行为之上,还有其他差异区分出生前后不同时间的造血干细胞。后者包括显示特定分化程序的造血干细胞比例变化,以及它们更新和自我更新控制的变化。在这里,我们总结了近期描述这些发育变化的研究、控制它们的一些机制,以及它们在理解白血病中与年龄相关的差异以及正常造血方面的潜在相关性。

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