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Cited 36 time in webofscience Cited 37 time in scopus
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Modulation of the caveolin-3 localization to caveolae and STAT3 to mitochondria by catecholamine-induced cardiac hypertrophy in H9c2 cardiomyoblastsopen access

Authors
Jeong, KyuhoKwon, HayeongMin, ChanheePak, Yunbae
Issue Date
30-Apr-2009
Publisher
NATURE PUBLISHING GROUP
Keywords
cardiomegaly; caveolae; caveolin-3; cell nucleus; heart; isoproterenol; mitochondria; phenylephrine; STAT3 transcription factor
Citation
EXPERIMENTAL AND MOLECULAR MEDICINE, v.41, no.4, pp 226 - 235
Pages
10
Indexed
SCIE
SCOPUS
KCI
Journal Title
EXPERIMENTAL AND MOLECULAR MEDICINE
Volume
41
Number
4
Start Page
226
End Page
235
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/26319
DOI
10.3858/emm.2009.41.4.025
ISSN
1226-3613
2092-6413
Abstract
We investigated the effect of phenylephrine (PE)- and isoproterenol (ISO)-induced cardiac hypertrophy on subcellular localization and expression of caveolin-3 and STAT3 in H9c2 cardiomyoblast cells. Caveolin-3 localization to plasma membrane was attenuated and localization of caveolin-3 to caveolae in the plasma membrane was 24.3% reduced by the catecholamine-induced hypertrophy. STAT3 and phospho-STAT3 were up-regulated but verapamill and cyclosporin A synergistically decreased the STAT3 and phospho-STAT3 levels in PE- and ISO-induced hypertrophic cells. Both expression and activation of STAT3 were increased in the nucleus by the hypertrophy. Immunofluorescence analysis revealed that the catecholamine-induced hypertrophy promoted nuclear localization of pY705-STAT3. Of interest, phosphorylation of pS727-STAT3 in mitochondria was significantly reduced by catecholamine-induced hypertrophy. In addition, mitochondrial complexes II and III were greatly down-regulated in the hypertrophic cells. Our data suggest that the alterations in nuclear and mitochondrial activation of STAT3 and caveolae localization of caveolin-3 are related to the development of the catecholamine-induced cardiac hypertrophy.
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