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干细胞中的同源框基因:维持细胞特性与分化调控

HOX genes in stem cells: Maintaining cellular identity and regulation of differentiation.

作者信息

Steens Jennifer, Klein Diana

机构信息

Institute for Cell Biology (Cancer Research), Medical Faculty, University of Duisburg-Essen, Essen, Germany.

出版信息

Front Cell Dev Biol. 2022 Sep 13;10:1002909. doi: 10.3389/fcell.2022.1002909. eCollection 2022.

Abstract

Stem cells display a unique cell type within the body that has the capacity to self-renew and differentiate into specialized cell types. Compared to pluripotent stem cells, adult stem cells (ASC) such as mesenchymal stem cells (MSCs) and hematopoietic stem cells (HSCs) exhibit restricted differentiation capabilities that are limited to cell types typically found in the tissue of origin, which implicates that there must be a certain code or priming determined by the tissue of origin. HOX genes, a subset of homeobox genes encoding transcription factors that are generally repressed in undifferentiated pluripotent stem cells, emerged here as master regulators of cell identity and cell fate during embryogenesis, and in maintaining this positional identity throughout life as well as specifying various regional properties of respective tissues. Concurrently, intricate molecular circuits regulated by diverse stem cell-typical signaling pathways, balance stem cell maintenance, proliferation and differentiation. However, it still needs to be unraveled how stem cell-related signaling pathways establish and regulate ASC-specific HOX expression pattern with different temporal-spatial topography, known as the HOX code. This comprehensive review therefore summarizes the current knowledge of specific ASC-related HOX expression patterns and how these were integrated into stem cell-related signaling pathways. Understanding the mechanism of HOX gene regulation in stem cells may provide new ways to manipulate stem cell fate and function leading to improved and new approaches in the field of regenerative medicine.

摘要

干细胞在体内呈现出一种独特的细胞类型,具有自我更新和分化为特定细胞类型的能力。与多能干细胞相比,成体干细胞(ASC),如间充质干细胞(MSC)和造血干细胞(HSC),表现出有限的分化能力,仅限于通常在其起源组织中发现的细胞类型,这意味着必定存在由起源组织决定的某种编码或启动机制。HOX基因是同源框基因的一个子集,编码转录因子,通常在未分化的多能干细胞中受到抑制,在此作为胚胎发育过程中细胞身份和细胞命运的主要调节因子出现,并在整个生命过程中维持这种位置身份,以及确定各个组织的各种区域特性。同时,由多种典型干细胞信号通路调节的复杂分子回路,平衡着干细胞的维持、增殖和分化。然而,干细胞相关信号通路如何建立和调节具有不同时空拓扑结构的ASC特异性HOX表达模式(即HOX编码),仍有待阐明。因此,这篇综述总结了目前关于特定ASC相关HOX表达模式的知识,以及这些模式如何整合到干细胞相关信号通路中。了解干细胞中HOX基因的调控机制可能为操纵干细胞命运和功能提供新方法,从而在再生医学领域带来改进和新的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34aa/9514042/ef558d055cf0/fcell-10-1002909-g001.jpg

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