Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries

Abstract: The injury phase after myocardial infarcts occurs during reperfusion and is a consequence of calcium release from internal stores combined with calcium entry, leading to cell death by apoptopic and necrotic processes. The mechanism(s) by which calcium enters cells has(ve) not been identifi...

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Autores principales: He, Xiju, Li, Shoutian, Liu, Benju, Susperreguy, Sebastián, Formoso, Karina, Yao, Jinghong, Kang, Jinsong, Anbing, Shi, Birnbaumer, Lutz, Liao, Yanhong
Formato: Artículo
Lenguaje:Inglés
Publicado: National Academy of Sciences 2019
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Acceso en línea:https://repositorio.uca.edu.ar/handle/123456789/8529
https://www.pnas.org/content/114/23/E4582
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id I33-R139123456789-8529
record_format dspace
institution Universidad Católica Argentina
institution_str I-33
repository_str R-139
collection Repositorio Institucional de la Universidad Católica Argentina (UCA)
language Inglés
topic INFARTO DEL MIOCARDIO
CALCIO
APOPTOSIS
MUERTE CELULAR
spellingShingle INFARTO DEL MIOCARDIO
CALCIO
APOPTOSIS
MUERTE CELULAR
He, Xiju
Li, Shoutian
Liu, Benju
Susperreguy, Sebastián
Formoso, Karina
Yao, Jinghong
Kang, Jinsong
Anbing, Shi
Birnbaumer, Lutz
Liao, Yanhong
Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
topic_facet INFARTO DEL MIOCARDIO
CALCIO
APOPTOSIS
MUERTE CELULAR
description Abstract: The injury phase after myocardial infarcts occurs during reperfusion and is a consequence of calcium release from internal stores combined with calcium entry, leading to cell death by apoptopic and necrotic processes. The mechanism(s) by which calcium enters cells has(ve) not been identified. Here, we identify canonical transient receptor potential channels (TRPC) 3 and 6 as the cation channels through which most of the damaging calcium enters cells to trigger their death, and we describe mechanisms activated during the injury phase. Working in vitro with H9c2 cardiomyoblasts subjected to 9-h hypoxia followed by 6-h reoxygenation (H/R), and analyzing changes occurring in areas-at-risk (AARs) of murine hearts subjected to a 30-min ischemia followed by 24-h reperfusion (I/R) protocol, we found: (i) that blocking TRPCwith SKF96365 significantly ameliorated damage induced by H/R, including development of the mitochondrial permeability transition and proapoptotic changes in Bcl2/BAX ratios; and (ii) that AAR tissues had increased TUNEL+ cells, augmented Bcl2/BAX ratios, and increased p(S240)NFATc3, p(S473) AKT, p(S9)GSK3β, and TRPC3 and -6 proteins, consistent with activation of a positive-feedback loop in which calcium entering through TRPCs activates calcineurin-mediated NFATc3-directed transcription of TRPC genes, leading to more Ca2+ entry. All these changes were markedly reduced in mice lacking TRPC3, -6, and -7. The changes caused by I/R in AAR tissues were matched by those seen after H/R in cardiomyoblasts in all aspects except for p-AKT and p-GSK3β, which were decreased after H/R in cardiomyoblasts instead of increased. TRPC should be promising targets for pharmacologic intervention after cardiac infarcts.
format Artículo
author He, Xiju
Li, Shoutian
Liu, Benju
Susperreguy, Sebastián
Formoso, Karina
Yao, Jinghong
Kang, Jinsong
Anbing, Shi
Birnbaumer, Lutz
Liao, Yanhong
author_facet He, Xiju
Li, Shoutian
Liu, Benju
Susperreguy, Sebastián
Formoso, Karina
Yao, Jinghong
Kang, Jinsong
Anbing, Shi
Birnbaumer, Lutz
Liao, Yanhong
author_sort He, Xiju
title Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
title_short Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
title_full Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
title_fullStr Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
title_full_unstemmed Major contribution of the 3/6/7 class of TRPC channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
title_sort major contribution of the 3/6/7 class of trpc channels to myocardial ischemia/reperfusion and cellular hypoxia/reoxygenation injuries
publisher National Academy of Sciences
publishDate 2019
url https://repositorio.uca.edu.ar/handle/123456789/8529
https://www.pnas.org/content/114/23/E4582
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