This Article Full Text Full Text (PDF) Data Supplement All Versions of this Article: 117/3/344    most recent CIRCULATIONAHA.107.695346v2 CIRCULATIONAHA.107.695346v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via HighWire Google Scholar Articles by Tsai, C.-T. Articles by Lin, J.-L. PubMed PubMed Citation Articles by Tsai, C.-T. Articles by Lin, J.-L. Pubmed/NCBI databases Gene GEO Profiles HomoloGene Nucleotide Protein UniGene Compound via MeSH Substance via MeSH Genetics Home Reference Hazardous Substances DB LOSARTAN POTASSIUM Related Collections ACE/Angiotension receptors Arrythmias-basic studies Related Article

(Circulation. 2008;117:344-355.)
© 2008 American Heart Association, Inc.

Arrhythmia/Electrophysiology

Angiotensin II Activates Signal Transducer and Activators of Transcription 3 via Rac1 in Atrial Myocytes and Fibroblasts

Implication for the Therapeutic Effect of Statin in Atrial Structural Remodeling

Chia-Ti Tsai, MD, PhD; Ling-Ping Lai, MD, PhD; Kuan-Ting Kuo, MD; Juey-Jen Hwang, MD, PhD; Chia-Shan Hsieh, MS; Kuan-Lih Hsu, MD, PhD; Chuen-Den Tseng, MD, PhD; Yung-Zu Tseng, MD; Fu-Tien Chiang, MD, PhD; Jiunn-Lee Lin, MD, PhD

From the Division of Cardiology, Department of Internal Medicine (C.-T.T., L.-P.L., J.-J.H., C.-S.H., K.-L.H., C.-D.T., Y.-Z.T., J.-L.L.), Department of Pathology (K.-T.K.), and Department of Laboratory Medicine (F.-T.C.), National Taiwan University Hospital, Taipei, Taiwan, and Institute of Pharmacology (L.-P.L.), National Taiwan University, Taipei, Taiwan.

Correspondence to Ling-Ping Lai, MD, PhD, Institute of Pharmacology, National Taiwan University or Jiunn-Lee Lin, MD, PhD, Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital, No. 1, Section 1, Jen-Ai Rd, Taipei 100, Taiwan. E-mail lplai2003{at}ntu.edu.tw

Received February 7, 2007; accepted October 26, 2007.

Background— Recently, activation of the local renin-angiotensin system and mitogen-activated protein kinase pathways in atrial myocardium has been found to play an important role in atrial structural remodeling related to atrial fibrillation. Another important mediator of the angiotensin II (Ang II) effect is the Janus kinase/signal transducers and activators of transcription (STAT) pathway, which has never been characterized in the atrium.

Methods and Results— In cultured atrial myocytes and fibroblasts, Ang II induced tyrosine phosphorylation of STAT3 through a Rac1-dependent mechanism, which was inhibited by dominant-negative Rac1, losartan, and simvastatin. In atrial myocytes, activation of STAT3 by Rac1 was mediated by direct association of Rac1 with STAT3; however, in atrial fibroblasts, it was mediated by an indirect paracrine effect. Constitutively active STAT3 increased protein synthesis, and dominant-negative STAT3 abrogated Ang II–induced protein synthesis in atrial myocytes and fibroblasts. Rats infused long term with Ang II exhibited higher levels of activated Rac1, phospho-STAT3, collagen synthesis, and atrial fibrosis in the atria, all of which were attenuated by oral losartan and simvastatin. In human atrial tissues from patients with atrial fibrillation, Ang II and phospho-STAT3 levels were also elevated.

Conclusions— The Ang II/Rac1/STAT3 pathway is an important signaling pathway in the atrial myocardium to mediate atrial structural remodeling, and losartan and statin may be able to reverse Ang II–induced atrial structural remodeling in atrial fibrillation.

---

 

CLINICAL PERSPECTIVE

Related Article:

Clinical Summaries
Circulation 2008 117: 331-332. [Full Text]

This article has been cited by other articles:

				D. Hilfiker-Kleiner and R. Knoll Disease-Modifying Mutations in Familial Hypertrophic Cardiomyopathy: Complexity From Simplicity Circulation, April 8, 2008; 117(14): 1775 - 1777. [Full Text] [PDF]

				M. C. Simeone-Penney, M. Severgnini, L. Rozo, S. Takahashi, B. H. Cochran, and A. R. Simon PDGF-induced human airway smooth muscle cell proliferation requires STAT3 and the small GTPase Rac1 Am J Physiol Lung Cell Mol Physiol, April 1, 2008; 294(4): L698 - L704. [Abstract] [Full Text] [PDF]