From proliferative to neurological role of an hsp70 stress chaperone, mortalin

Although the brain makes up approximately 2% of a person's body weight, it consumes more than 15% of total cardiac output and has a per capita caloric requirement of 10 times more than the rest of the body. Such continuous metabolic demand that supports the generation of action potentials in ne...

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Main Authors: Deocaris, Custer C., Kaul, Sunil C., Wadhwa, Renu
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Published: Animo Repository 2008
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Online Access:https://animorepository.dlsu.edu.ph/faculty_research/5473
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Institution: De La Salle University
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spelling oai:animorepository.dlsu.edu.ph:faculty_research-62452022-04-20T02:17:22Z From proliferative to neurological role of an hsp70 stress chaperone, mortalin Deocaris, Custer C. Kaul, Sunil C. Wadhwa, Renu Although the brain makes up approximately 2% of a person's body weight, it consumes more than 15% of total cardiac output and has a per capita caloric requirement of 10 times more than the rest of the body. Such continuous metabolic demand that supports the generation of action potentials in neuronal cells relies on the mitochondria, the main organelle for power generation. The phenomenon of mitochondrial biogenesis, although has long been a neglected theme in neurobiology, can be regarded as critical to brain physiology. The present review emphasizes the role of a key molecular player of mitochondrial biogenesis, the mortalin/mthsp70. Brain mortalin is discussed in relation to its aptitude to impact on mitochondrial function and homeostasis, to its interfacing energy metabolic functions with synaptic plasticity, and to its modulation of brain aging via the cellular senescence pathways. Recently, this chaperone has been implicated in Alzheimer's (AD) and Parkinson's (PD) diseases, with proteomic studies consistently identifying oxidatively-damaged mortalin as potential biomarker. Hence, it is possible that mitochondrial dysfunction coincides with the collapse in the mitochondrial chaperone network that aim not only to import, sort and maintain integrity of protein components within the mitochondria, but also to act as buffer to the molecular heterogeneity of damaged and aging mitochondrial proteins within a ROS-rich microenvironment. Inversely, it may also seem that vulnerability to mitochondrial dysfunction could be precipitated by malevolent (anti-chaperone) gain-of-function of a 'sick mortalin'. 2008-12-01T08:00:00Z text https://animorepository.dlsu.edu.ph/faculty_research/5473 Faculty Research Work Animo Repository Molecular chaperones Mitochondria Oxidative stress Nervous system—Degeneration Developmental neurobiology Biology Neuroscience and Neurobiology
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
topic Molecular chaperones
Mitochondria
Oxidative stress
Nervous system—Degeneration
Developmental neurobiology
Biology
Neuroscience and Neurobiology
spellingShingle Molecular chaperones
Mitochondria
Oxidative stress
Nervous system—Degeneration
Developmental neurobiology
Biology
Neuroscience and Neurobiology
Deocaris, Custer C.
Kaul, Sunil C.
Wadhwa, Renu
From proliferative to neurological role of an hsp70 stress chaperone, mortalin
description Although the brain makes up approximately 2% of a person's body weight, it consumes more than 15% of total cardiac output and has a per capita caloric requirement of 10 times more than the rest of the body. Such continuous metabolic demand that supports the generation of action potentials in neuronal cells relies on the mitochondria, the main organelle for power generation. The phenomenon of mitochondrial biogenesis, although has long been a neglected theme in neurobiology, can be regarded as critical to brain physiology. The present review emphasizes the role of a key molecular player of mitochondrial biogenesis, the mortalin/mthsp70. Brain mortalin is discussed in relation to its aptitude to impact on mitochondrial function and homeostasis, to its interfacing energy metabolic functions with synaptic plasticity, and to its modulation of brain aging via the cellular senescence pathways. Recently, this chaperone has been implicated in Alzheimer's (AD) and Parkinson's (PD) diseases, with proteomic studies consistently identifying oxidatively-damaged mortalin as potential biomarker. Hence, it is possible that mitochondrial dysfunction coincides with the collapse in the mitochondrial chaperone network that aim not only to import, sort and maintain integrity of protein components within the mitochondria, but also to act as buffer to the molecular heterogeneity of damaged and aging mitochondrial proteins within a ROS-rich microenvironment. Inversely, it may also seem that vulnerability to mitochondrial dysfunction could be precipitated by malevolent (anti-chaperone) gain-of-function of a 'sick mortalin'.
format text
author Deocaris, Custer C.
Kaul, Sunil C.
Wadhwa, Renu
author_facet Deocaris, Custer C.
Kaul, Sunil C.
Wadhwa, Renu
author_sort Deocaris, Custer C.
title From proliferative to neurological role of an hsp70 stress chaperone, mortalin
title_short From proliferative to neurological role of an hsp70 stress chaperone, mortalin
title_full From proliferative to neurological role of an hsp70 stress chaperone, mortalin
title_fullStr From proliferative to neurological role of an hsp70 stress chaperone, mortalin
title_full_unstemmed From proliferative to neurological role of an hsp70 stress chaperone, mortalin
title_sort from proliferative to neurological role of an hsp70 stress chaperone, mortalin
publisher Animo Repository
publishDate 2008
url https://animorepository.dlsu.edu.ph/faculty_research/5473
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