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组织金属蛋白酶抑制剂3促进小鼠脑室下区神经干祖细胞的维持。

TIMP3 promotes the maintenance of neural stem-progenitor cells in the mouse subventricular zone.

作者信息

Fang Lingyan, Kuniya Takaaki, Harada Yujin, Yasuda Osamu, Maeda Nobuyo, Suzuki Yutaka, Kawaguchi Daichi, Gotoh Yukiko

机构信息

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.

Department of Sports and Life Sciences, National Institute of Fitness and Sports in Kanoya, Kanoya, Japan.

出版信息

Front Neurosci. 2023 Jun 28;17:1149603. doi: 10.3389/fnins.2023.1149603. eCollection 2023.

Abstract

Adult neural stem cells (NSCs) in the mouse subventricular zone (SVZ) serve as a lifelong reservoir for newborn olfactory bulb neurons. Recent studies have identified a slowly dividing subpopulation of embryonic neural stem-progenitor cells (NPCs) as the embryonic origin of adult NSCs. Yet, little is known about how these slowly dividing embryonic NPCs are maintained until adulthood while other NPCs are extinguished by the completion of brain development. The extracellular matrix (ECM) is an essential component of stem cell niches and thus a key determinant of stem cell fate. Here we investigated tissue inhibitors of metalloproteinases (TIMPs)-regulators of ECM remodeling-for their potential roles in the establishment of adult NSCs. We found that , , and were expressed at high levels in slowly dividing NPCs compared to rapidly dividing NPCs. Deletion of TIMP3 reduced the number of adult NSCs and neuroblasts in the lateral SVZ. In addition, overexpression of TIMP3 in the embryonic NPCs suppressed neuronal differentiation and upregulated the expression levels of Notch signaling relating genes. These results thus suggest that TIMP3 keeps the undifferentiated state of embryonic NPCs, leading to the establishment and maintenance of adult NSCs.

摘要

小鼠脑室下区(SVZ)中的成年神经干细胞(NSCs)是新生嗅球神经元的终身储备库。最近的研究已确定胚胎神经干祖细胞(NPCs)中有一个分裂缓慢的亚群是成年神经干细胞的胚胎起源。然而,对于这些分裂缓慢的胚胎神经祖细胞如何维持到成年期,而其他神经祖细胞在脑发育完成时消失,我们却知之甚少。细胞外基质(ECM)是干细胞微环境的重要组成部分,因此是干细胞命运的关键决定因素。在这里,我们研究了金属蛋白酶组织抑制剂(TIMPs)——细胞外基质重塑的调节因子——在成年神经干细胞建立过程中的潜在作用。我们发现,与快速分裂的神经祖细胞相比,TIMPs在分裂缓慢的神经祖细胞中高表达。TIMP3的缺失减少了外侧脑室下区成年神经干细胞和神经母细胞的数量。此外,在胚胎神经祖细胞中过表达TIMP3可抑制神经元分化,并上调Notch信号相关基因的表达水平。因此,这些结果表明TIMP3维持了胚胎神经祖细胞的未分化状态,从而导致成年神经干细胞的建立和维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/922d/10338847/f6e9b72b4d16/fnins-17-1149603-g001.jpg

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