Liu Min, Xu Ping, O'Brien Timothy, Shen Sanbing
Regenerative Medicine Institute, School of Medicine, National University of Ireland (NUI) Galway, Galway, Ireland.
State Key Laboratory of Proteomics, National Center for Protein Sciences, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, Beijing Institute of Radiation Medicine, Beijing, China.
Neurogenesis (Austin). 2017 May 23;4(1):e1313646. doi: 10.1080/23262133.2017.1313646. eCollection 2017.
Neurogenesis is essential for proper brain formation and function, and abnormal neural proliferation is an underlying neuropathology of many brain disorders. Recent advances on adult neurogenesis demonstrate that neural stem cells (NSCs) at the subventricular zone (SVZ) are largely derived during mid-embryonic neurogenesis from a subset of cells, which slow down in their pace of cell division, become quiescent cells and can be reactivated in need. The NSCs at birth constitute the stem cell pool for both postnatal oligodendrogenesis and adult neurogenesis. However, little is known about factors that control the size of NSC pool. The article published in Stem Cells on Jun 14, 2016 by Liu and colleagues described a member of the Unc-51-like serine/threonine kinase family, Ulk4, which plays a critical role in regulating the NSC pool size. Authors presented evidence of cell cycle-dependent Ulk4 expression and , and reduced NSC pool in targetedly disrupted newborn mice, with disturbed pathways of cell cycle regulation and WNT signaling (Fig. 1), suggesting that ULK4 may be associated with neurodevelopmental, neuropsychiatric as well as neurodegenerative diseases.
神经发生对于正常的大脑形成和功能至关重要,而异常的神经增殖是许多脑部疾病的潜在神经病理学特征。关于成体神经发生的最新进展表明,脑室下区(SVZ)的神经干细胞(NSCs)在胚胎中期神经发生期间主要来源于一部分细胞,这些细胞的细胞分裂速度减慢,成为静止细胞,并可在需要时重新激活。出生时的神经干细胞构成了出生后少突胶质细胞生成和成体神经发生的干细胞库。然而,对于控制神经干细胞库大小的因素知之甚少。刘及其同事于2016年6月14日发表在《干细胞》杂志上的文章描述了Unc-51样丝氨酸/苏氨酸激酶家族的成员Ulk4,它在调节神经干细胞库大小方面起着关键作用。作者提供了细胞周期依赖性Ulk4表达的证据,以及在新生小鼠中靶向破坏后神经干细胞库减少的证据,同时细胞周期调节和WNT信号通路受到干扰(图1),这表明ULK4可能与神经发育、神经精神以及神经退行性疾病有关。