• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2024, Vol. 26 ›› Issue (6): 818-824.DOI: 10.3969/j.issn.1671-2587.2024.06.018

• 综述 • 上一篇    下一篇

mTOR通路在调控造血干细胞自我更新和分化中的研究进展*

王嘉琪1, 肖军2, 李翠莹1,2   

  1. 1河北北方学院,河北张家口 075000;
    2空军军医大学空军特色医学中心输血科,北京 100142
  • 收稿日期:2024-07-01 出版日期:2024-12-20 发布日期:2024-12-20
  • 通讯作者: 李翠莹,主要从事临床输血及免疫血液学研究工作,(E-mail)licuiying2013@qq.com。
  • 作者简介:王嘉琪,主要从事临床检验诊断学及临床输血学研究工作,(E-mail)15832303086@163.com。
  • 基金资助:
    *本课题受空军军医大学效能提升项目(No.2021HKYX15)、空军特色医学中心青年人才项目(No.22BJQN009)资助

Research Progress of mTOR Pathway in Regulating Self-renewal and Differentiation of Hematopoietic Stem Cells

WANG Jiaqi1, XIAO Jun2, LI Cuiying1,2   

  1. 1Graduate School of Hebei North University, Zhangjiakou, Hebei Province 075000;
    2Department of Blood Transfusion, Air Force Medical Center, Beijing 100142
  • Received:2024-07-01 Online:2024-12-20 Published:2024-12-20

摘要: 哺乳动物雷帕霉素靶蛋白(mammalian target of rapamycin, mTOR)是一种丝/苏氨酸蛋白激酶,在调节细胞的生长、增殖中起着重要的作用。mTOR复合体通过磷酸化激活下游底物S6K1、4E-BP等调节细胞生长、增殖、蛋白质代谢等等,同样mTOR信号通路在造血系统中也发挥重要作用,其整合多种信号对造血干细胞的静止、自我更新和多向分化三个过程起调节作用,本文系统介绍相关信号分子及蛋白如何通过影响mTOR信号通路并进一步影响造血干细胞发挥功能。

关键词: 造血干细胞, mTOR信号通路, 造血分化, 自我更新, 恶性造血

Abstract: The mammalian target of rapamycin (mTOR) is a serine/threonine protein kinase that plays an important role in regulating cell growth, proliferation.The mTOR complex regulates cell growth, proliferation, protein metabolism by phosphorylating and activating downstream substrates such as S6K1, 4E-BP, etc. The mTOR signalling pathway similarly plays an important role in the haematopoietic system, integrating multiple signals to regulate the three processes of haematopoietic stem cell quiescence, self-renewal and multidirectional differentiation.This article systematically describes how relevant signalling molecules and proteins affect the mTOR signalling pathway and further influence haematopoietic stem cell function.

Key words: Haematopoietic stem cells, mTOR signalling pathway, Haematopoietic differentiation, Self-renewal, Malignant haemopoiesis

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