Primary cilium and brain aging: role in neural stem cells, neurodegenerative diseases and glioblastoma

被引:24
|
作者
Alvarez-Satta, Maria [1 ]
Moreno-Cugnon, Leire [1 ]
Matheu, Ander [1 ,2 ,3 ]
机构
[1] Biodonostia Hlth Res Inst, Cellular Oncol Grp, Paseo Dr Beguiristain S-N, San Sebastian 20014, Spain
[2] CIBER Fragilidad & Envejecimiento Saludable CIBER, Madrid, Spain
[3] Basque Fdn, Ikerbasque, Bilbao, Spain
关键词
Primary cilium; Aging; Neural stem cells; Stem cell exhaustion; Neurodegenerative diseases; Glioblastoma; AGE-RELATED-CHANGES; HIPPOCAMPAL NEUROGENESIS; SUBVENTRICULAR ZONE; CELLULAR SENESCENCE; SELF-RENEWAL; CILIOGENESIS; PROLIFERATION; DEPLETION; DECLINE; CANCER;
D O I
10.1016/j.arr.2019.04.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Brain aging is characterized by a progressive loss of tissue integrity and function as a consequence of impaired homeostasis and regeneration capacities. The primary cilium is a highly conserved organelle that projects from the cell surface in a single copy in virtually all mammalian cell types including neural stem/progenitors cells and neurons. Increasing evidence in the last decade points out that primary cilium could be a relevant mediator of neural stem cell activity, neurogenesis, neuronal maturation and maintenance, and brain tumorigenesis. In this review, we summarize the current knowledge about primary cilia roles in these processes. There is currently sufficient background to propose that defective primary cilia contribute to age-related cognitive decline and brain tumor development due to their critical roles in cell cycle control and signaling transduction. This might have potential applications on therapy against age-associated brain diseases.
引用
收藏
页码:53 / 63
页数:11
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