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p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart.

Publication ,  Journal Article
Li, M; Georgakopoulos, D; Lu, G; Hester, L; Kass, DA; Hasday, J; Wang, Y
Published in: Circulation
May 17, 2005

BACKGROUND: Increasing evidence suggests that development of heart failure involves activation of stress-response inflammatory cytokines, including tumor necrosis factor-alpha and interleukin-6. Yet, the myocyte contribution to their induction in failing hearts and the underlying regulatory mechanism in stressed myocardium remain unclear. METHODS AND RESULTS: In cultured cardiac myocytes, specific activation of stress-activated mitogen-activated protein kinase, p38, by upstream activator MKK6bE led to significant induction of tumor necrosis factor-alpha and interleukin-6 secretion, whereas treating cells with a selective p38 inhibitor (SB239068) significantly blocked the cytokine secretion from myocytes and increased their intracellular accumulation. Targeted expression of MKK6bE in transgenic hearts also resulted in a marked elevation in plasma tumor necrosis factor-alpha and interleukin-6; oral administration of SB239068 resulted in a significant reduction in their plasma levels but an increase in intracardiac accumulation of both cytokines. MKK6bE transgenic hearts developed marked interstitial fibrosis with increased matrix metalloproteinase abundance and selective induction of tissue inhibitor of matrix metalloproteinase-1; this extracellular matrix remodeling was also significantly attenuated by p38 inhibition. Along with cytokine induction and extracellular remodeling, MKK6bE transgenic animals displayed impaired hemodynamic function, whereas p38 inhibition improved the cardiac performance and prolonged the survival of the animals. CONCLUSIONS: Stress-activated p38 kinase is a critical regulator of inflammatory response in cardiomyocytes with significant contribution to pathological remodeling in stressed myocardium. Inhibition of p38 may represent a useful therapeutic avenue to ameliorate cardiac pathology and heart failure evolution.

Duke Scholars

Published In

Circulation

DOI

EISSN

1524-4539

Publication Date

May 17, 2005

Volume

111

Issue

19

Start / End Page

2494 / 2502

Location

United States

Related Subject Headings

  • p38 Mitogen-Activated Protein Kinases
  • Tumor Necrosis Factor-alpha
  • Rats, Sprague-Dawley
  • Rats
  • Myocytes, Cardiac
  • Mice, Transgenic
  • Mice
  • Interleukin-6
  • Inflammation
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
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Li, M., Georgakopoulos, D., Lu, G., Hester, L., Kass, D. A., Hasday, J., & Wang, Y. (2005). p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart. Circulation, 111(19), 2494–2502. https://doi.org/10.1161/01.CIR.0000165117.71483.0C
Li, Manxiang, Dimitrios Georgakopoulos, Gang Lu, Lisa Hester, David A. Kass, Jeffery Hasday, and Yibin Wang. “p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart.Circulation 111, no. 19 (May 17, 2005): 2494–2502. https://doi.org/10.1161/01.CIR.0000165117.71483.0C.
Li M, Georgakopoulos D, Lu G, Hester L, Kass DA, Hasday J, et al. p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart. Circulation. 2005 May 17;111(19):2494–502.
Li, Manxiang, et al. “p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart.Circulation, vol. 111, no. 19, May 2005, pp. 2494–502. Pubmed, doi:10.1161/01.CIR.0000165117.71483.0C.
Li M, Georgakopoulos D, Lu G, Hester L, Kass DA, Hasday J, Wang Y. p38 MAP kinase mediates inflammatory cytokine induction in cardiomyocytes and extracellular matrix remodeling in heart. Circulation. 2005 May 17;111(19):2494–2502.

Published In

Circulation

DOI

EISSN

1524-4539

Publication Date

May 17, 2005

Volume

111

Issue

19

Start / End Page

2494 / 2502

Location

United States

Related Subject Headings

  • p38 Mitogen-Activated Protein Kinases
  • Tumor Necrosis Factor-alpha
  • Rats, Sprague-Dawley
  • Rats
  • Myocytes, Cardiac
  • Mice, Transgenic
  • Mice
  • Interleukin-6
  • Inflammation
  • Humans