ATM modulates subventricular zone neural stem cell maintenance and senescence through Notch signaling pathway

被引:10
|
作者
Dong, Chuanming [1 ,2 ]
Wang, Xianli [5 ]
Sun, Lixin [2 ]
Zhu, Liang [2 ]
Yang, Danjing [2 ]
Gao, Shane
Zhang, Wenjun [3 ]
Ling, Bin [6 ]
Liang, Aibin [3 ]
Gao, Zhengliang [4 ]
Xu, Jun [2 ]
机构
[1] Nantong Univ, Dept Anat, Nantong 226001, Peoples R China
[2] Tongji Univ Sch Med, East Hosp, Shanghai 200120, Peoples R China
[3] Tongji Univ Sch Med, Tongji Hosp, Dept Hematol, Shanghai 200065, Peoples R China
[4] Tongji Univ Sch Med, Shanghai Peoples Hosp 10, Shanghai 200072, Peoples R China
[5] Shanghai Jiao Tong Univ Sch Med, Dept Biochem & Mol Cell Biol, Shanghai Key Lab Tumor Microenvironm & Inflammat, Key Lab Cell Differentiat, Shanghai 200025, Peoples R China
[6] Second Peoples Hosp Yunnan Prov, Kunming 650021, Peoples R China
基金
中国国家自然科学基金;
关键词
ATM; Neural stem cell; Notch signaling pathway; Quiescence; Aging; DNA-DAMAGE RESPONSE; SELF-RENEWAL; ATAXIA-TELANGIECTASIA; OXIDATIVE STRESS; REPAIR; QUIESCENT; NEUROGENESIS; INSTABILITY; ACTIVATION; MECHANISMS;
D O I
10.1016/j.scr.2021.102618
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Ataxia telangiectasia mutated (ATM) plays an essential role in DNA damage response and the maintenance of genomic stability. However, the role of ATM in regulating the function of adult neural stem cells (NSCs) remains unclear. Here we report that ATM deficiency led to accumulated DNA damage and decreased DNA damage repair capacity in neural progenitor cells. Moreover, we observed ATM ablation lead to the short-term increase of proliferation of neural progenitor cells, resulting in the depletion of the NSC pool over time, and this loss of NSC quiescence resulted in accelerated cell senescence. We further apply RNA sequencing to unravel that ATM knockout significantly affected Notch signaling pathway, furthermore, notch activation inhibit the abnormal increased proliferation of ATM-/- NSCs. Taken together, these findings indicate that ATM can serve as a key regulator for the normal function of adult NSCs by maintaining their stemness and preventing cellular senescence primarily through Notch signaling pathway.
引用
收藏
页数:13
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