King's College London

Research portal

Activation of p38 mitogen-activated protein kinase contributes to the early cardiodepressant action of tumor necrosis factor

Research output: Contribution to journalArticle

M Bellahcene, S Jacquet, X B Cao, M Tanno, R S Haworth, J Layland, A M Kabir, M Gaestel, R J Davis, R A Flavell, A M Shah, M Avkiran, M S Marber

Original languageEnglish
Pages (from-to)545 - 555
Number of pages11
JournalJournal of the American College of Cardiology
Volume48
Issue number3
DOIs
Publication statusPublished - 1 Aug 2006

King's Authors

Abstract

OBJECTIVES The purpose of this study was to determine whether p38 mitogen-activated protein kinase (p38-MAPK) contributes to tumor necrosis factor-alpha (TNF alpha)-induced contractile depression. BACKGROUND Tumor necrosis factor has both beneficial and detrimental consequences that may result from the activation of different downstream pathways. Tumor necrosis factor activates p38-MAPK, a stress-responsive kinase implicated in contractile depression and cardiac injury. METHODS In isolated hearts from mice lacking the p38-MAPK activator, MAPK kinase 3 (MKK3), perfused at constant coronary pressure or flow, we measured the left ventricular developed pressure (LVDP) and the relationship between end-diastolic volume and LVDP in the presence and absence of 10 ng/ml TNF alpha. RESULTS Within 15 min at constant pressure, TNF alpha significantly reduced LVDP and coronary flow in outbred and mkk3(+/+) mice. This early negative inotropic effect was associated with a marked phosphorylation of both p38-MAPK and its indirect substrate, HSP27. In hearts lacking MKK3, TNF alpha failed to activate p38-MAPK or to cause significant contractile dysfunction. The actions of TNF alpha were similarly attenuated in MAPK-activated protein kinase 2 (MK2)-deficient hearts, which have a marked reduction in myocardial p38-MAPK protein content, and by the p38-MAPK catalytic site inhibitor SB203580 (1 mu mol/l). Under conditions of constant coronary flow, the p38-MAPK activation and contractile depression induced by TNF alpha, though attenuated, remained sensitive to the absence of MKK3 or the presence of SB203580. The role of p38-MAPK in TNF alpha-induced contractile depression was confirmed in isolated murine cardiac myocytes exposed to SB203580 or lacking MKK3. CONCLUSIONS Tumor necrosis factor activates p38-MAPK in the intact heart and in isolated cardiac myocytes through MKK3. This activation likely contributes to the early cardiodepressant action of TNF alpha

View graph of relations

© 2018 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454