自噬
神经保护
自闭症谱系障碍
神经科学
自闭症
生物
午睡
精神分裂症(面向对象编程)
微管
医学
细胞生物学
遗传学
精神科
细胞凋亡
作者
Shlomo Sragovich,Avia Merenlender‐Wagner,Illana Gozes
出处
期刊:BioEssays
[Wiley]
日期:2017-09-21
卷期号:39 (11)
被引量:51
标识
DOI:10.1002/bies.201700054
摘要
Activity‐dependent neuroprotective protein (ADNP), discovered in our laboratory in 1999, has been characterized as a master gene vital for mammalian brain formation. ADNP de novo mutations in humans result in a syndromic form of autism‐like spectrum disorder (ASD), including cognitive and motor deficits, the ADNP syndrome ( Helsmoortel‐Van Der Aa ). One of the most important cellular processes associated with ADNP is the autophagy pathway, recently discovered by us as a key player in the pathophysiology of schizophrenia. In this regard, given the link between the microtubule and autophagy systems, the ADNP microtubule end binding protein motif, namely, the neuroprotective NAP (NAPVSIPQ), was found to enhance autophagy while protecting microtubules and augmenting ADNP's association with both systems. Thus, linking autophagy and ADNP is proposed as a major target for intervention in brain diseases from autism to Alzheimer's disease (AD) and our findings introduce autophagy as a possible novel target for treating schizophrenia.
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