生物
造血
基因组学
干细胞
谱系(遗传)
计算生物学
进化生物学
遗传学
基因
基因组
作者
L. Alexander Liggett,Vijay G. Sankaran
出处
期刊:Cell
[Cell Press]
日期:2020-09-01
卷期号:182 (6): 1384-1400
被引量:121
标识
DOI:10.1016/j.cell.2020.08.030
摘要
Hematopoiesis has long served as a paradigm of stem cell biology and tissue homeostasis. In the past decade, the genomics revolution has ushered in powerful new methods for investigating the hematopoietic system that have provided transformative insights into its biology. As part of the advances in genomics, increasingly accurate deep sequencing and novel methods of cell tracking have revealed hematopoiesis to be more of a continuous and less of a discrete and punctuated process than originally envisioned. In part, this continuous nature of hematopoiesis is made possible by the emergent outcomes of vast, interconnected regulatory networks that influence cell fates and lineage commitment. It is also becoming clear how these mechanisms are modulated by genetic variation present throughout the population. This review describes how these recently uncovered complexities are reshaping our concept of tissue development and homeostasis while opening up a more comprehensive future understanding of hematopoiesis.
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