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Tsukushi 对于维持和终末分化小鼠海马神经干细胞是必需的。

Tsukushi is essential for proper maintenance and terminal differentiation of mouse hippocampal neural stem cells.

机构信息

Department of Developmental Neurobiology, Graduate School of Life Sciences, Kumamoto University, Kumamoto, Japan.

Stem Cell-Based Tissue Regeneration Research and Education Unit, Kumamoto University, Kumamoto, Japan.

出版信息

Dev Growth Differ. 2020 Feb;62(2):108-117. doi: 10.1111/dgd.12649. Epub 2020 Jan 26.

Abstract

Secreted proteoglycan molecule Tsukushi (TSK) regulates various developmental processes, such as early body patterning and neural plate formation by interacting with major signaling pathways like Wnt, BMP, Notch etc. In central nervous system, TSK inhibits Wnt signaling to control chick retinal development. It also plays important roles for axon guidance and anterior commissure formation in mouse brain. In the present study, we investigated the role of TSK for the development and proper functioning of mouse hippocampus. We found that TSK expression is prominent at hippocampal regions of early postnatal mouse until postnatal day 15 and gradually declines at later stages. Hippocampal dimensions are affected in TSK knockout mice (TSK-KO) as shown by reduced size of hippocampus and dentate gyrus (DG). Interestingly, neural stem cell (NSC) density at the neural niche of DG was higher in TSK-KO compared with wild-type. The ratio of proliferating NSCs as well as the rate of overall cell proliferation was also higher in TSK-KO hippocampus. Our in vitro study also suggests an increased number of neural stem/progenitor cells residing in TSK-KO hippocampus. Finally, we found that the terminal differentiation of NSCs in TSK-KO was disturbed as the differentiation to neuronal cell lineage was increased while the percentages of astrocytes and oligodendrocytes were decreased. Overall, our study establishes the involvement of TSK in hippocampal development, NSC maintenance and terminal differentiation at perinatal stages.

摘要

分泌型蛋白聚糖分子 Tsukushi(TSK)通过与 Wnt、BMP、Notch 等主要信号通路相互作用,调节各种发育过程,如早期体模式形成和神经板形成。在中枢神经系统中,TSK 抑制 Wnt 信号以控制鸡视网膜发育。它在小鼠大脑中的轴突导向和前连合形成中也起着重要作用。在本研究中,我们研究了 TSK 对小鼠海马体发育和正常功能的作用。我们发现,TSK 在新生后小鼠的海马区表达明显,直到出生后第 15 天,然后在后期逐渐下降。TSK 敲除小鼠(TSK-KO)的海马体尺寸受到影响,表现为海马体和齿状回(DG)减小。有趣的是,与野生型相比,TSK-KO 中的 DG 神经巢区的神经干细胞(NSC)密度更高。TSK-KO 海马体中的增殖 NSCs 比例和总体细胞增殖率也更高。我们的体外研究还表明,TSK-KO 海马体中存在更多数量的神经干细胞/祖细胞。最后,我们发现 TSK-KO 中的 NSCs 终末分化受到干扰,因为向神经元细胞谱系的分化增加,而星形胶质细胞和少突胶质细胞的百分比减少。总体而言,我们的研究确立了 TSK 参与围产期海马体发育、NSC 维持和终末分化的作用。

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