首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >AGING OF THE SUBVENTRICULAR ZONE NEURAL STEM CELL NICHE: EVIDENCE FOR QUIESCENCE-ASSOCIATED CHANGES BETWEEN EARLY AND MID-ADULTHOOD
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AGING OF THE SUBVENTRICULAR ZONE NEURAL STEM CELL NICHE: EVIDENCE FOR QUIESCENCE-ASSOCIATED CHANGES BETWEEN EARLY AND MID-ADULTHOOD

机译:室下区神经干细胞壁CHE的老化:早期和中期成年患者静默相关变化的证据

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Stem cells can exist in either active or quiescent states. In the aging hippocampus, adult neural stem cells (aNSCs) shift into a quiescent state, contributing to age-related reductions in hippocampal neurogenesis. Here, we focused on the subventricular zone (SVZ) stem cell niche of the adult forebrain, asking to what extent quiescence-associated changes in aNSCs are initiated between early and middle-age. Immunohistochemical and label retention experiments revealed that the overall output of the SVZ stem cell system was already highly decreased in middle-aged mice (12-months-old) compared with young adult mice (2-month-old), as measured by reduced marker expression for multiple neural precursor sub-populations and diminished addition of SVZ-derived neuroblasts to the olfactory bulbs (OBs). These changes were associated with significant cytological aberrations within the SVZ niche, including an overall atrophy of the SVZ and accumulation of large lipid droplets within ependymal cells, which are key support cells of the SVZ niche. Importantly, the reduced output of the middle-aged SVZ stem cell system correlated with quiescence-associated changes in middle-aged aNSCs. Specifically, while tissue culture experiments showed that young adult and middle-aged fore-brains possessed equal numbers of neurosphere-forming aNSCs, the middle-aged neurospheres exhibited differences in their in vitro properties, and middle-aged aNSCs in vivo divided less frequently. These findings demonstrate that aNSCs begin undergoing quiescence-associated changes between early and mid-adulthood in the mouse SVZ, and serve as a useful framework for further studies aimed at defining the early events involved in aging-associated quiescence of aNSCs.
机译:干细胞可以以活跃或静止状态存在。在衰老的海马中,成年神经干细胞(aNSC)转变为静止状态,导致与年龄相关的海马神经发生减少。在这里,我们集中于成年前脑的脑室下区(SVZ)干细胞生态位,询问aNSCs的静止相关变化在多大程度上在早期和中年之间引发。免疫组织化学和标记物保留实验表明,与年轻成年小鼠(2个月大)相比,中年小鼠(12个月大)的SVZ干细胞系统的总产量已经大大降低,这是通过减少标记来测量的表达多个神经前体亚群,并减少了嗅球(OB)中SVZ衍生的成神经细胞的添加。这些变化与SVZ生态位内的明显细胞学畸变有关,包括SVZ的整体萎缩和室管膜细胞内大量脂质液滴的积累,这些细胞是SVZ生态位的关键支持细胞。重要的是,中年SVZ干细胞系统输出的减少与中年aNSC的静止相关变化有关。具体而言,虽然组织培养实验显示,年轻的成年和中年前脑拥有相等数量的神经球形成aNSC,但中年神经球在体外特性上表现出差异,而中年aNSC在体内的分裂频率则较低。这些发现表明,aNSCs在小鼠SVZ的成年早期和成年之间开始经历与静止有关的变化,并为进一步研究提供有用的框架,该研究旨在确定与aNSC的衰老相关的静止所涉及的早期事件。

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