Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.
Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA; Integrative Biosciences Department, School of Dentistry, Oregon Health & Science University, Portland, OR 97239, USA.
Matrix Biol. 2019 May;78-79:272-283. doi: 10.1016/j.matbio.2018.01.022. Epub 2018 Jan 31.
Adult neurogenesis in mammals is a tightly regulated process where neural stem cells (NSCs), especially in the subgranular zone (SGZ) of the hippocampal dentate gyrus, proliferate and differentiate into new neurons that form new circuits or integrate into old circuits involved in episodic memory, pattern discrimination, and emotional responses. Recent evidence suggests that changes in the hyaluronan (HA)-based extracellular matrix of the SGZ may regulate neurogenesis by controlling NSC proliferation and early steps in neuronal differentiation. These studies raise the intriguing possibility that perturbations in this matrix, including HA accumulation with aging, could impact adult neurogenesis and cognitive functions, and that alterations to this matrix could be beneficial following insults to the central nervous system that impact hippocampal functions.
哺乳动物的成年神经发生是一个受到严格调控的过程,其中神经干细胞(NSCs),特别是在海马齿状回的颗粒下区(SGZ)中,增殖并分化为新的神经元,形成新的回路或整合到参与情景记忆、模式识别和情绪反应的旧回路中。最近的证据表明,SGZ 中基于透明质酸(HA)的细胞外基质的变化可能通过控制 NSC 增殖和神经元分化的早期步骤来调节神经发生。这些研究提出了一个有趣的可能性,即这种基质的扰动,包括随着年龄增长而积累的 HA,可能会影响成年神经发生和认知功能,并且这种基质的改变可能对中枢神经系统受到影响海马功能的损伤后有益。