利基
造血
胎儿
电流(流体)
干细胞
国家(计算机科学)
造血干细胞
生物
细胞生物学
计算机科学
怀孕
遗传学
工程类
生态学
电气工程
算法
作者
Harsh Agrawal,Shubham Haribhau Mehatre,Satish Khurana
标识
DOI:10.1016/j.exphem.2024.104585
摘要
Hematopoietic development goes through a number of embryonic sites that host hematopoietic progenitor and stem cells with function required at specific developmental stages. Among embryonic sites, the fetal liver (FL) hosts definitive hematopoietic stem cells (HSCs) capable of engrafting adult hematopoietic system and supports their rapid expansion. Hence, this site provides an excellent model to understand the cellular and molecular components of the machinery involved in HSC-proliferative events, leading to their overall expansion. It has been unequivocally established that extrinsic regulators orchestrate events that maintain HSC function. Although most studies on extrinsic regulation of HSC function are targeted at adult bone marrow (BM) hematopoiesis, little is known about how FL HSC function is regulated by their microniche. This review provides the current state of our understanding on molecular and cellular niche factors that support FL hematopoiesis.
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