Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.

Relationships between αB-crystallin expression patterns and pathological changes of myocardial cells after heat stress were examined in vitro and in vivo in this study using the H9C2 cell line and Sprague-Dawley rats, respectively. Histopathological lesions, characterized by acute degeneration, kary...

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Main Authors: Shu Tang, Yingjun Lv, Hongbo Chen, Abdelnasir Adam, Yanfen Cheng, Jörg Hartung, Endong Bao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24466295/?tool=EBI
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spelling doaj-4050d83b38d548f885988ae2f13af0fa2021-03-03T19:47:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8693710.1371/journal.pone.0086937Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.Shu TangYingjun LvHongbo ChenAbdelnasir AdamYanfen ChengJörg HartungEndong BaoRelationships between αB-crystallin expression patterns and pathological changes of myocardial cells after heat stress were examined in vitro and in vivo in this study using the H9C2 cell line and Sprague-Dawley rats, respectively. Histopathological lesions, characterized by acute degeneration, karyopyknosis and loss of a defined nucleus, became more severe in rat hearts over the course of heat stress treatment from 20 min to 100 min. The expression of αB-crystallin in rat hearts showed a significant decrease (P<0.05) throughout the heat stress treatment period, except at the 40 min time point. Likewise, decreased αB-crystallin expression was also observed in the H9C2 cell line exposed to a high temperature in vitro, although its expression recovered to normal levels at later time points (80 and 100 min) and the cellular damage was less severe. The results suggest that αB-crystallin is mobilized early after exposure to a high temperature to interact with damaged proteins but that the myocardial cells cannot produce sufficient αB-crystallin for protection against heat stress. Lower αB-crystallin expression levels were accompanied by obvious cell/tissue damage, suggesting that the abundance of this protein is associated with protective effects in myocardial cells in vitro and in vivo. Thus, αB-crystallin is a potential biomarker of heat stress.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24466295/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Shu Tang
Yingjun Lv
Hongbo Chen
Abdelnasir Adam
Yanfen Cheng
Jörg Hartung
Endong Bao
spellingShingle Shu Tang
Yingjun Lv
Hongbo Chen
Abdelnasir Adam
Yanfen Cheng
Jörg Hartung
Endong Bao
Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
PLoS ONE
author_facet Shu Tang
Yingjun Lv
Hongbo Chen
Abdelnasir Adam
Yanfen Cheng
Jörg Hartung
Endong Bao
author_sort Shu Tang
title Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
title_short Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
title_full Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
title_fullStr Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
title_full_unstemmed Comparative analysis of αB-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
title_sort comparative analysis of αb-crystallin expression in heat-stressed myocardial cells in vivo and in vitro.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Relationships between αB-crystallin expression patterns and pathological changes of myocardial cells after heat stress were examined in vitro and in vivo in this study using the H9C2 cell line and Sprague-Dawley rats, respectively. Histopathological lesions, characterized by acute degeneration, karyopyknosis and loss of a defined nucleus, became more severe in rat hearts over the course of heat stress treatment from 20 min to 100 min. The expression of αB-crystallin in rat hearts showed a significant decrease (P<0.05) throughout the heat stress treatment period, except at the 40 min time point. Likewise, decreased αB-crystallin expression was also observed in the H9C2 cell line exposed to a high temperature in vitro, although its expression recovered to normal levels at later time points (80 and 100 min) and the cellular damage was less severe. The results suggest that αB-crystallin is mobilized early after exposure to a high temperature to interact with damaged proteins but that the myocardial cells cannot produce sufficient αB-crystallin for protection against heat stress. Lower αB-crystallin expression levels were accompanied by obvious cell/tissue damage, suggesting that the abundance of this protein is associated with protective effects in myocardial cells in vitro and in vivo. Thus, αB-crystallin is a potential biomarker of heat stress.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24466295/?tool=EBI
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