CSCR (Wellcome Trust Centre for Stem Cell Research), Tennis Court Road, Cambridge CB2 1QR, UK.
Biochem J. 2012 Jul 1;445(1):1-10. doi: 10.1042/BJ20120401.
Regulation of stem cells is essential for development and adult tissue homoeostasis. The proper control of stem cell self-renewal and differentiation maintains organ physiology, and disruption of such a balance results in disease. There are many mechanisms that have been established as stem cell regulators, such as Wnt or Notch signals. However, the intracellular mechanisms that mediate and integrate these signals are not well understood. A new intracellular pathway that has been reported to be involved in the regulation of many stem cell types is that of p38 MAPK (mitogen-activated protein kinase). In particular, p38α is essential for the proper differentiation of many haematopoietic, mesenchymal and epithelial stem/progenitor cells. Many reports have shown that disruption of this kinase pathway has pathological consequences in many organs. Understanding the extracellular cues and downstream targets of p38α in stem cell regulation may help to tackle some of the pathologies associated with improper differentiation and regulation of stem cell function. In the present review we present a vision of the current knowledge on the roles of the p38α signal as a regulator of stem/progenitor cells in different tissues in physiology and disease.
干细胞的调控对于发育和成人组织稳态至关重要。干细胞自我更新和分化的适当控制维持着器官的生理功能,而这种平衡的破坏会导致疾病。已经确定了许多作为干细胞调节剂的机制,如 Wnt 或 Notch 信号。然而,介导和整合这些信号的细胞内机制尚不清楚。已经有报道称,参与许多干细胞类型调控的一个新的细胞内途径是 p38 MAPK(丝裂原活化蛋白激酶)途径。特别是,p38α 对于许多造血、间充质和上皮干细胞/祖细胞的适当分化是必不可少的。许多报道表明,该激酶途径的破坏会导致许多器官的病理后果。了解 p38α 在干细胞调控中的细胞外线索和下游靶标,可能有助于解决与干细胞功能不当分化和调控相关的一些病理学问题。在本综述中,我们提出了目前关于 p38α 信号作为不同组织中干细胞/祖细胞调节因子在生理和疾病中的作用的认识。