TGF-β1 affects cell-cell adhesion in the heart in an NCAM1-dependent mechanism

Maegen A. Ackermann, Jennifer M. Petrosino, Heather R. Manring, Patrick Wright, Vikram Shettigar, Ahmet Kilic, Paul M.L. Janssen, Mark T. Ziolo, Federica Accornero

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

The contractile property of the myocardium is maintained by cell-cell junctions enabling cardiomyocytes to work as a syncytium. Alterations in cell-cell junctions are observed in heart failure, a disease characterized by the activation of Transforming Growth Factor beta 1 (TGFβ1). While TGFβ1 has been implicated in diverse biologic responses, its molecular function in controlling cell-cell adhesion in the heart has never been investigated. Cardiac-specific transgenic mice expressing active TGFβ1 were generated to model the observed increase in activity in the failing heart. Activation of TGFβ1 in the heart was sufficient to drive ventricular dysfunction. To begin to understand the function of this important molecule we undertook an extensive structural analysis of the myocardium by electron microscopy and immunostaining. This approach revealed that TGFβ1 alters intercalated disc structures and cell-cell adhesion in ventricular myocytes. Mechanistically, we found that TGFβ1 induces the expression of neural adhesion molecule 1 (NCAM1) in cardiomyocytes in a p38-dependent pathway, and that selective targeting of NCAM1 was sufficient to rescue the cell adhesion defect observed when cardiomyocytes were treated with TGFβ1. Importantly, NCAM1 was upregulated in human heart samples from ischemic and non-ischemic cardiomyopathy patients and NCAM1 protein levels correlated with the degree of TGFβ1 activity in the human cardiac ventricle. Overall, we found that TGFβ1 is deleterious to the heart by regulating the adhesion properties of cardiomyocytes in an NCAM1-dependent mechanism. Our results suggest that inhibiting NCAM1 would be cardioprotective, counteract the pathological action of TGFβ1 and reduce heart failure severity.

Original languageEnglish (US)
Pages (from-to)49-57
Number of pages9
JournalJournal of Molecular and Cellular Cardiology
Volume112
DOIs
StatePublished - Nov 2017
Externally publishedYes

Keywords

  • Cell adhesion
  • Heart failure
  • Intercalated disc
  • NCAM1
  • TGFβ1

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

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