Andreas Christoper, Herry Herman, Rizky Abdulah, Felix Zulhendri, Ardo Sanjaya, Ronny Lesmana
{"title":"Physiological Roles of Hippo Signaling Pathway and Autophagy in Dementia.","authors":"Andreas Christoper, Herry Herman, Rizky Abdulah, Felix Zulhendri, Ardo Sanjaya, Ronny Lesmana","doi":"10.2174/1874609816666230206144212","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Dementia is a neurocognitive disorder associated with the aging brain and mainly affects the hippocampus and cerebral cortex. The Hippo signaling pathway and autophagy proteins have been found to be perturbed in the brain affected by dementia processes.</p><p><strong>Objective: </strong>This systematic review aims to elaborate on the involvement of the Hippo signaling pathway and autophagy in modulating the progression and severity of dementia in aging.</p><p><strong>Methods: </strong>Searches were conducted on MEDLINE, Google Scholar, Scopus, and Web of Science databases.</p><p><strong>Results: </strong>The Hippo signaling pathway is dependent upon the transcriptional co-activator YAP/TAZ, which forms complexes with TEAD in the nucleus in order to maintain cell homeostasis. When the expression YAP/TAZ is reduced, transcriptional repression-induced atypical cell death, ballooning cell death, and necrosis will consequently occur in the neurons. Moreover, the autophagic proteins, such as LC3, ATG proteins, and Beclin, are reduced, resulting in the disruption of autophagosome formation and accumulation and the spread of misfolded proteins in the brain suffering from dementia.</p><p><strong>Conclusion: </strong>The impairment of the Hippo signaling pathway and autophagy in the dementia process in aging should be considered since it might predict the severity, treatment, and prevention of dementia.</p>","PeriodicalId":11008,"journal":{"name":"Current aging science","volume":"16 2","pages":"112-124"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current aging science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874609816666230206144212","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1
Abstract
Background: Dementia is a neurocognitive disorder associated with the aging brain and mainly affects the hippocampus and cerebral cortex. The Hippo signaling pathway and autophagy proteins have been found to be perturbed in the brain affected by dementia processes.
Objective: This systematic review aims to elaborate on the involvement of the Hippo signaling pathway and autophagy in modulating the progression and severity of dementia in aging.
Methods: Searches were conducted on MEDLINE, Google Scholar, Scopus, and Web of Science databases.
Results: The Hippo signaling pathway is dependent upon the transcriptional co-activator YAP/TAZ, which forms complexes with TEAD in the nucleus in order to maintain cell homeostasis. When the expression YAP/TAZ is reduced, transcriptional repression-induced atypical cell death, ballooning cell death, and necrosis will consequently occur in the neurons. Moreover, the autophagic proteins, such as LC3, ATG proteins, and Beclin, are reduced, resulting in the disruption of autophagosome formation and accumulation and the spread of misfolded proteins in the brain suffering from dementia.
Conclusion: The impairment of the Hippo signaling pathway and autophagy in the dementia process in aging should be considered since it might predict the severity, treatment, and prevention of dementia.
背景:痴呆是一种与大脑老化相关的神经认知障碍,主要影响海马和大脑皮层。已经发现Hippo信号通路和自噬蛋白在受痴呆过程影响的大脑中受到干扰。目的:本系统综述旨在阐述Hippo信号通路和自噬在调节老年痴呆进展和严重程度中的作用。方法:在MEDLINE、Google Scholar、Scopus和Web of Science数据库中进行检索。结果:Hippo信号通路依赖于转录共激活因子YAP/TAZ, YAP/TAZ在细胞核中与TEAD形成复合物以维持细胞稳态。当YAP/TAZ的表达减少时,转录抑制诱导的非典型细胞死亡、球囊细胞死亡和神经元坏死就会发生。此外,自噬蛋白如LC3、ATG蛋白、Beclin蛋白减少,导致自噬小体的形成和积累被破坏,错误折叠蛋白在痴呆脑内扩散。结论:老年痴呆过程中Hippo信号通路和自噬的损伤可能预示痴呆的严重程度、治疗和预防,应予以考虑。