Valny Martin, Honsa Pavel, Kriska Jan, Anderova Miroslava
Department of Cellular Neurophysiology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Department of Cellular Neurophysiology, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Biochem Pharmacol. 2017 Oct 1;141:42-55. doi: 10.1016/j.bcp.2017.05.008. Epub 2017 May 15.
NG2 cells represent one of the most proliferative glial cell populations in the intact mammalian central nervous system (CNS). They are well-known for their ability to renew themselves or to generate new oligodendrocytes during development as well as in adulthood, therefore also being termed oligodendrocyte progenitor cells. Following CNS injuries, such as demyelination, trauma or ischemia, the proliferative capacity of NG2 cells rapidly increases and moreover, their differentiation potential broadens, as documented by numerous reports also describing their differentiation into astrocytes or even neurons. Here, we summarize the current knowledge about NG2 cells proliferation, their fate plasticity during embryogenesis as well as in postnatal CNS under physiological and pathological conditions, with the main emphasis on the role of various signaling molecules, growth factors, hormones or even neurotransmitters on the fate potential of NG2 cells.
NG2细胞是完整哺乳动物中枢神经系统(CNS)中增殖能力最强的胶质细胞群体之一。它们以在发育过程以及成年期自我更新或产生新的少突胶质细胞的能力而闻名,因此也被称为少突胶质细胞前体细胞。中枢神经系统损伤后,如脱髓鞘、创伤或缺血,NG2细胞的增殖能力迅速增强,此外,其分化潜能也会扩大,许多报告都证明了这一点,这些报告还描述了它们分化为星形胶质细胞甚至神经元的情况。在这里,我们总结了目前关于NG2细胞增殖、它们在胚胎发育过程中以及出生后中枢神经系统在生理和病理条件下的命运可塑性的知识,主要强调各种信号分子、生长因子、激素甚至神经递质对NG2细胞命运潜能的作用。