Raghu Padinjat, Joseph Annu, Krishnan Harini, Singh Pramod, Saha Sankhanil
National Centre for Biological Sciences-TIFR, Bengaluru, India.
Front Mol Neurosci. 2019 Aug 23;12:208. doi: 10.3389/fnmol.2019.00208. eCollection 2019.
Phosphoinositides, the seven phosphorylated derivatives of phosphatidylinositol have emerged as regulators of key sub-cellular processes such as membrane transport, cytoskeletal function and plasma membrane signaling in eukaryotic cells. All of these processes are also present in the cells that constitute the nervous system of animals and in this setting too, these are likely to tune key aspects of cell biology in relation to the unique structure and function of neurons. Phosphoinositides metabolism and function are mediated by enzymes and proteins that are conserved in evolution, and analysis of knockouts of these in animal models implicate this signaling system in neural function. Most recently, with the advent of human genome analysis, mutations in genes encoding components of the phosphoinositide signaling pathway have been implicated in human diseases although the cell biological basis of disease phenotypes in many cases remains unclear. In this review we evaluate existing evidence for the involvement of phosphoinositide signaling in human nervous system diseases and discuss ways of enhancing our understanding of the role of this pathway in the human nervous system's function in health and disease.
磷脂酰肌醇的七种磷酸化衍生物——磷酸肌醇,已成为真核细胞中关键亚细胞过程的调节因子,这些过程包括膜运输、细胞骨架功能和质膜信号传导。动物神经系统的组成细胞中也存在所有这些过程,在这种情况下,它们也可能调节与神经元独特结构和功能相关的细胞生物学关键方面。磷酸肌醇的代谢和功能由进化上保守的酶和蛋白质介导,对动物模型中这些基因敲除的分析表明该信号系统与神经功能有关。最近,随着人类基因组分析的出现,编码磷酸肌醇信号通路成分的基因突变已被认为与人类疾病有关,尽管在许多情况下疾病表型的细胞生物学基础仍不清楚。在这篇综述中,我们评估了磷酸肌醇信号传导参与人类神经系统疾病的现有证据,并讨论了增强我们对该信号通路在人类神经系统健康和疾病功能中作用理解的方法。