Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation

Chia Ti Tsai, Jiunn Lee Lin, Ling Ping Lai, Chih Sheng Lin, Sheoi K Stephen Huang

研究成果: 雜誌貢獻文章

31 引文 (Scopus)

摘要

Background: Angiotensin II and its downstream mitogen-activated protein kinase signaling pathways are involved in the pathogenesis of AF. Pro-inflammatory JAK/STAT is another downstream signaling pathway of Angiotensin II, and its status in AF remains unknown. Objective: The aim of this study was to characterize the status of the Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathways in pacing-induced sustained atrial fibrillation (AF). Methods: AF was induced by atrial pacing at 600/min in 10 adult pigs (AF group), while 10 sham-operated pigs served as the control group. Results: Significant structural and inflammatory changes were noted in the AF group. Atrial tissue angiotensin II level was elevated and STAT1 and STAT3 were activated in the AF group. Nuclear translocation of activated STAT3 and binding to STAT3 consensus DNA sequence were also increased in the AF group. Rac1, the molecular target of statin, which mediates the activation of STAT3 by angiotensin II, was also activated in the AF group. The tissue levels of interleukin-6, leukemia inhibitory factor (LIF) and cardiotrophin-1 (CT-1), which are known to activate STATs through membrane gp130 and JAKs, were not increased in the AF group. Membrane gp130 and JAKs were also not activated in the AF group. Conclusion: Activated angiotensin II/Rac1/STAT may be associated with or perhaps contribute to the structural and inflammatory changes in pacing-induced sustained trial fibrillation. It may further imply the therapeutic option of combination of angiotensin receptor blocker and statin.
原文英語
頁(從 - 到)1285-1293
頁數9
期刊Heart Rhythm
5
發行號9
DOIs
出版狀態已發佈 - 九月 1 2008
對外發佈Yes

指紋

Monomeric GTP-Binding Proteins
Atrial Fibrillation
Membranes
Angiotensin II
Janus Kinases
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Transducers
Swine
Leukemia Inhibitory Factor
Angiotensin Receptor Antagonists
Consensus Sequence
Mitogen-Activated Protein Kinases
Interleukin-6

Keywords

  • Angiotensin II
  • Atrial fibrillation
  • Janus kinase/signal transducers and activators of transcription
  • Mitogen-activated protein kinase
  • Rac1
  • Small GTPase

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

引用此文

Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation. / Tsai, Chia Ti; Lin, Jiunn Lee; Lai, Ling Ping; Lin, Chih Sheng; Huang, Sheoi K Stephen.

於: Heart Rhythm, 卷 5, 編號 9, 01.09.2008, p. 1285-1293.

研究成果: 雜誌貢獻文章

Tsai, Chia Ti ; Lin, Jiunn Lee ; Lai, Ling Ping ; Lin, Chih Sheng ; Huang, Sheoi K Stephen. / Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation. 於: Heart Rhythm. 2008 ; 卷 5, 編號 9. 頁 1285-1293.
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abstract = "Background: Angiotensin II and its downstream mitogen-activated protein kinase signaling pathways are involved in the pathogenesis of AF. Pro-inflammatory JAK/STAT is another downstream signaling pathway of Angiotensin II, and its status in AF remains unknown. Objective: The aim of this study was to characterize the status of the Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathways in pacing-induced sustained atrial fibrillation (AF). Methods: AF was induced by atrial pacing at 600/min in 10 adult pigs (AF group), while 10 sham-operated pigs served as the control group. Results: Significant structural and inflammatory changes were noted in the AF group. Atrial tissue angiotensin II level was elevated and STAT1 and STAT3 were activated in the AF group. Nuclear translocation of activated STAT3 and binding to STAT3 consensus DNA sequence were also increased in the AF group. Rac1, the molecular target of statin, which mediates the activation of STAT3 by angiotensin II, was also activated in the AF group. The tissue levels of interleukin-6, leukemia inhibitory factor (LIF) and cardiotrophin-1 (CT-1), which are known to activate STATs through membrane gp130 and JAKs, were not increased in the AF group. Membrane gp130 and JAKs were also not activated in the AF group. Conclusion: Activated angiotensin II/Rac1/STAT may be associated with or perhaps contribute to the structural and inflammatory changes in pacing-induced sustained trial fibrillation. It may further imply the therapeutic option of combination of angiotensin receptor blocker and statin.",
keywords = "Angiotensin II, Atrial fibrillation, Janus kinase/signal transducers and activators of transcription, Mitogen-activated protein kinase, Rac1, Small GTPase, Angiotensin II, Atrial fibrillation, Janus kinase/signal transducers and activators of transcription, Mitogen-activated protein kinase, Rac1, Small GTPase",
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TY - JOUR

T1 - Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation

AU - Tsai, Chia Ti

AU - Lin, Jiunn Lee

AU - Lai, Ling Ping

AU - Lin, Chih Sheng

AU - Huang, Sheoi K Stephen

PY - 2008/9/1

Y1 - 2008/9/1

N2 - Background: Angiotensin II and its downstream mitogen-activated protein kinase signaling pathways are involved in the pathogenesis of AF. Pro-inflammatory JAK/STAT is another downstream signaling pathway of Angiotensin II, and its status in AF remains unknown. Objective: The aim of this study was to characterize the status of the Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathways in pacing-induced sustained atrial fibrillation (AF). Methods: AF was induced by atrial pacing at 600/min in 10 adult pigs (AF group), while 10 sham-operated pigs served as the control group. Results: Significant structural and inflammatory changes were noted in the AF group. Atrial tissue angiotensin II level was elevated and STAT1 and STAT3 were activated in the AF group. Nuclear translocation of activated STAT3 and binding to STAT3 consensus DNA sequence were also increased in the AF group. Rac1, the molecular target of statin, which mediates the activation of STAT3 by angiotensin II, was also activated in the AF group. The tissue levels of interleukin-6, leukemia inhibitory factor (LIF) and cardiotrophin-1 (CT-1), which are known to activate STATs through membrane gp130 and JAKs, were not increased in the AF group. Membrane gp130 and JAKs were also not activated in the AF group. Conclusion: Activated angiotensin II/Rac1/STAT may be associated with or perhaps contribute to the structural and inflammatory changes in pacing-induced sustained trial fibrillation. It may further imply the therapeutic option of combination of angiotensin receptor blocker and statin.

AB - Background: Angiotensin II and its downstream mitogen-activated protein kinase signaling pathways are involved in the pathogenesis of AF. Pro-inflammatory JAK/STAT is another downstream signaling pathway of Angiotensin II, and its status in AF remains unknown. Objective: The aim of this study was to characterize the status of the Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathways in pacing-induced sustained atrial fibrillation (AF). Methods: AF was induced by atrial pacing at 600/min in 10 adult pigs (AF group), while 10 sham-operated pigs served as the control group. Results: Significant structural and inflammatory changes were noted in the AF group. Atrial tissue angiotensin II level was elevated and STAT1 and STAT3 were activated in the AF group. Nuclear translocation of activated STAT3 and binding to STAT3 consensus DNA sequence were also increased in the AF group. Rac1, the molecular target of statin, which mediates the activation of STAT3 by angiotensin II, was also activated in the AF group. The tissue levels of interleukin-6, leukemia inhibitory factor (LIF) and cardiotrophin-1 (CT-1), which are known to activate STATs through membrane gp130 and JAKs, were not increased in the AF group. Membrane gp130 and JAKs were also not activated in the AF group. Conclusion: Activated angiotensin II/Rac1/STAT may be associated with or perhaps contribute to the structural and inflammatory changes in pacing-induced sustained trial fibrillation. It may further imply the therapeutic option of combination of angiotensin receptor blocker and statin.

KW - Angiotensin II

KW - Atrial fibrillation

KW - Janus kinase/signal transducers and activators of transcription

KW - Mitogen-activated protein kinase

KW - Rac1

KW - Small GTPase

KW - Angiotensin II

KW - Atrial fibrillation

KW - Janus kinase/signal transducers and activators of transcription

KW - Mitogen-activated protein kinase

KW - Rac1

KW - Small GTPase

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U2 - 10.1016/j.hrthm.2008.05.012

DO - 10.1016/j.hrthm.2008.05.012

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JO - Heart Rhythm

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SN - 1547-5271

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