Literature DB >> 27197071

Disorders of lysosomal acidification-The emerging role of v-ATPase in aging and neurodegenerative disease.

Daniel J Colacurcio1, Ralph A Nixon2.   

Abstract

Autophagy and endocytosis deliver unneeded cellular materials to lysosomes for degradation. Beyond processing cellular waste, lysosomes release metabolites and ions that serve signaling and nutrient sensing roles, linking the functions of the lysosome to various pathways for intracellular metabolism and nutrient homeostasis. Each of these lysosomal behaviors is influenced by the intraluminal pH of the lysosome, which is maintained in the low acidic range by a proton pump, the vacuolar ATPase (v-ATPase). New reports implicate altered v-ATPase activity and lysosomal pH dysregulation in cellular aging, longevity, and adult-onset neurodegenerative diseases, including forms of Parkinson disease and Alzheimer disease. Genetic defects of subunits composing the v-ATPase or v-ATPase-related proteins occur in an increasingly recognized group of familial neurodegenerative diseases. Here, we review the expanding roles of the v-ATPase complex as a platform regulating lysosomal hydrolysis and cellular homeostasis. We discuss the unique vulnerability of neurons to persistent low level lysosomal dysfunction and review recent clinical and experimental studies that link dysfunction of the v-ATPase complex to neurodegenerative diseases across the age spectrum. Copyright Â
© 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acidification; Alzheimer’s disease; Autophagy; Calcium; Caloric restriction; Cathepsin; Endocytosis; Lysosomal storage disease; Lysosome; Parkinson’s disease; TFEB; mTORC; pH; v-ATPase

Mesh:

Substances:

Year:  2016        PMID: 27197071      PMCID: PMC5112157          DOI: 10.1016/j.arr.2016.05.004

Source DB:  PubMed          Journal:  Ageing Res Rev        ISSN: 1568-1637            Impact factor:   10.895


  236 in total

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Review 6.  Amyloid precursor protein and endosomal-lysosomal dysfunction in Alzheimer's disease: inseparable partners in a multifactorial disease.

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7.  Protein homeostasis of a metastable subproteome associated with Alzheimer's disease.

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Review 8.  Role of endolysosomes and inter-organellar signaling in brain disease.

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10.  Loss of TMEM106B Ameliorates Lysosomal and Frontotemporal Dementia-Related Phenotypes in Progranulin-Deficient Mice.

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