Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke

Abstract: The seven canonical members of transient receptor potential (TRPC) proteins form cation channels that evoke membrane depolarization and intracellular calcium concentration ([Ca2C]i) rise, which are not only important for regulating cell function but their deregulation can also lead to cell damage. Recent studies have implicated complex roles of TRPC channels in neurodegenerative diseases including ischemic stroke. Brain ischemia reduces oxygen and glucose supply to neurons, i.e., Oxygen and Glucose Deprivation (OGD), resulting in [Ca2C]i elevation, ion dyshomeostasis, and excitotoxicity, which are also common in many forms of neurodegenerative diseases. Although ionotropic glutamate receptors, e.g., N-methyl-D-aspartate receptors, are well established to play roles in excitotoxicity, the contribution of metabotropic glutamate receptors and their downstream effectors, i.e., TRPC channels, should not be neglected. Here, we summarize the current findings about contributions of TRPC channels in neurodegenerative diseases, with a focus on OGD-induced neuronal death and rodent models of cerebral ischemia/reperfusion. TRPC channels play both detrimental and protective roles to neurodegeneration depending on the TRPC subtype and specific pathological conditions involved. When illustrated the mechanisms by which TRPC channels are involved in neuronal survival or death seem differ greatly, implicating diverse and complex regulation. We provide our own data showing that TRPC1/C4/C5, especially TRPC4, may be generally detrimental in OGD and cerebral ischemia/reperfusion. We propose that although TRPC channels significantly contribute to ischemic neuronal death, detailed mechanisms and specific roles of TRPC subtypes in brain injury at different stages of ischemia/reperfusion and in different brain regions need to be carefully and systematically investigated.

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Main Authors: Jeon, Jaepyo, Bu, Fan, Sun, Guanghua, Tian, Jin-Bin, Ting, Shun-Ming, Li, Jun, Aronowski, Jaroslaw, Birnbaumer, Lutz, Freichel, Marc, Zhu, Michael X.
Format: Artículo biblioteca
Language:eng
Published: Lausanne: Frontiers Media 2021
Subjects:TRCP, FISIOPATOLOGÍA, ENFERMEDADES NEURODEGENERATIVAS, ACCIDENTE CEREBROVASCULAR, LESION CEREBRAL,
Online Access:https://repositorio.uca.edu.ar/handle/123456789/11624
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spelling oai:ucacris:123456789-116242023-11-22T21:51:11Z Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke Jeon, Jaepyo Bu, Fan Sun, Guanghua Tian, Jin-Bin Ting, Shun-Ming Li, Jun Aronowski, Jaroslaw Birnbaumer, Lutz Freichel, Marc Zhu, Michael X. TRCP FISIOPATOLOGÍA ENFERMEDADES NEURODEGENERATIVAS ACCIDENTE CEREBROVASCULAR LESION CEREBRAL Abstract: The seven canonical members of transient receptor potential (TRPC) proteins form cation channels that evoke membrane depolarization and intracellular calcium concentration ([Ca2C]i) rise, which are not only important for regulating cell function but their deregulation can also lead to cell damage. Recent studies have implicated complex roles of TRPC channels in neurodegenerative diseases including ischemic stroke. Brain ischemia reduces oxygen and glucose supply to neurons, i.e., Oxygen and Glucose Deprivation (OGD), resulting in [Ca2C]i elevation, ion dyshomeostasis, and excitotoxicity, which are also common in many forms of neurodegenerative diseases. Although ionotropic glutamate receptors, e.g., N-methyl-D-aspartate receptors, are well established to play roles in excitotoxicity, the contribution of metabotropic glutamate receptors and their downstream effectors, i.e., TRPC channels, should not be neglected. Here, we summarize the current findings about contributions of TRPC channels in neurodegenerative diseases, with a focus on OGD-induced neuronal death and rodent models of cerebral ischemia/reperfusion. TRPC channels play both detrimental and protective roles to neurodegeneration depending on the TRPC subtype and specific pathological conditions involved. When illustrated the mechanisms by which TRPC channels are involved in neuronal survival or death seem differ greatly, implicating diverse and complex regulation. We provide our own data showing that TRPC1/C4/C5, especially TRPC4, may be generally detrimental in OGD and cerebral ischemia/reperfusion. We propose that although TRPC channels significantly contribute to ischemic neuronal death, detailed mechanisms and specific roles of TRPC subtypes in brain injury at different stages of ischemia/reperfusion and in different brain regions need to be carefully and systematically investigated. 2021-06-15T13:07:19Z 2021-06-15T13:07:19Z 2021 Artículo Jeon, J., et al. Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke [en línea]. Frontiers in cell and developmental biology. 2021, 8. doi: 10.3389/fcell.2020.618663. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/11624 2296-634X (on line) https://repositorio.uca.edu.ar/handle/123456789/11624 10.3389/fcell.2020.618663 33490083 eng Acceso abierto http://creativecommons.org/licenses/by-nc-sa/4.0/ application/pdf Lausanne: Frontiers Media Frontiers in cell and developmental biology. 2021, 8
institution UCA
collection DSpace
country Argentina
countrycode AR
component Bibliográfico
access En linea
databasecode dig-uca
tag biblioteca
region America del Sur
libraryname Sistema de bibliotecas de la UCA
language eng
topic TRCP
FISIOPATOLOGÍA
ENFERMEDADES NEURODEGENERATIVAS
ACCIDENTE CEREBROVASCULAR
LESION CEREBRAL
TRCP
FISIOPATOLOGÍA
ENFERMEDADES NEURODEGENERATIVAS
ACCIDENTE CEREBROVASCULAR
LESION CEREBRAL
spellingShingle TRCP
FISIOPATOLOGÍA
ENFERMEDADES NEURODEGENERATIVAS
ACCIDENTE CEREBROVASCULAR
LESION CEREBRAL
TRCP
FISIOPATOLOGÍA
ENFERMEDADES NEURODEGENERATIVAS
ACCIDENTE CEREBROVASCULAR
LESION CEREBRAL
Jeon, Jaepyo
Bu, Fan
Sun, Guanghua
Tian, Jin-Bin
Ting, Shun-Ming
Li, Jun
Aronowski, Jaroslaw
Birnbaumer, Lutz
Freichel, Marc
Zhu, Michael X.
Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
description Abstract: The seven canonical members of transient receptor potential (TRPC) proteins form cation channels that evoke membrane depolarization and intracellular calcium concentration ([Ca2C]i) rise, which are not only important for regulating cell function but their deregulation can also lead to cell damage. Recent studies have implicated complex roles of TRPC channels in neurodegenerative diseases including ischemic stroke. Brain ischemia reduces oxygen and glucose supply to neurons, i.e., Oxygen and Glucose Deprivation (OGD), resulting in [Ca2C]i elevation, ion dyshomeostasis, and excitotoxicity, which are also common in many forms of neurodegenerative diseases. Although ionotropic glutamate receptors, e.g., N-methyl-D-aspartate receptors, are well established to play roles in excitotoxicity, the contribution of metabotropic glutamate receptors and their downstream effectors, i.e., TRPC channels, should not be neglected. Here, we summarize the current findings about contributions of TRPC channels in neurodegenerative diseases, with a focus on OGD-induced neuronal death and rodent models of cerebral ischemia/reperfusion. TRPC channels play both detrimental and protective roles to neurodegeneration depending on the TRPC subtype and specific pathological conditions involved. When illustrated the mechanisms by which TRPC channels are involved in neuronal survival or death seem differ greatly, implicating diverse and complex regulation. We provide our own data showing that TRPC1/C4/C5, especially TRPC4, may be generally detrimental in OGD and cerebral ischemia/reperfusion. We propose that although TRPC channels significantly contribute to ischemic neuronal death, detailed mechanisms and specific roles of TRPC subtypes in brain injury at different stages of ischemia/reperfusion and in different brain regions need to be carefully and systematically investigated.
format Artículo
topic_facet TRCP
FISIOPATOLOGÍA
ENFERMEDADES NEURODEGENERATIVAS
ACCIDENTE CEREBROVASCULAR
LESION CEREBRAL
author Jeon, Jaepyo
Bu, Fan
Sun, Guanghua
Tian, Jin-Bin
Ting, Shun-Ming
Li, Jun
Aronowski, Jaroslaw
Birnbaumer, Lutz
Freichel, Marc
Zhu, Michael X.
author_facet Jeon, Jaepyo
Bu, Fan
Sun, Guanghua
Tian, Jin-Bin
Ting, Shun-Ming
Li, Jun
Aronowski, Jaroslaw
Birnbaumer, Lutz
Freichel, Marc
Zhu, Michael X.
author_sort Jeon, Jaepyo
title Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
title_short Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
title_full Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
title_fullStr Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
title_full_unstemmed Contribution of TRPC channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
title_sort contribution of trpc channels in neuronal excitotoxicity associated with neurodegenerative disease and ischemic stroke
publisher Lausanne: Frontiers Media
publishDate 2021
url https://repositorio.uca.edu.ar/handle/123456789/11624
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