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β-catenin downregulation attenuates ischemic cardiac remodeling through enhanced resident precursor cell differentiation

Item Type:Article
Title:β-catenin downregulation attenuates ischemic cardiac remodeling through enhanced resident precursor cell differentiation
Creators Name:Zelarayan, L.C. and Noack, C. and Sekkali, B. and Kmecova, J. and Gehrke, C. and Renger, A. and Zafiriou, M.P. and van der Nagel, R. and Dietz, R. and de Windt, L.J. and Balligand, J.L. and Bergmann, M.W.
Abstract:We analyzed the effect of conditional, alphaMHC-dependent genetic beta-catenin depletion and stabilization on cardiac remodeling following experimental infarct. beta-Catenin depletion significantly improved 4-week survival and left ventricular (LV) function (fractional shortening: CT(Deltaex3-6): 24 +/- 1.9%; beta-cat(Deltaex3-6): 30.2 +/- 1.6%, P < 0.001). beta-Catenin stabilization had opposite effects. No significant changes in adult cardiomyocyte survival or hypertrophy were observed in either transgenic line. Associated with the functional improvement, LV scar cellularity was altered: beta-catenin-depleted mice showed a marked subendocardial and subepicardial layer of small cTnT(pos) cardiomyocytes associated with increased expression of cardiac lineage markers Tbx5 and GATA4. Using a Cre-dependent lacZ reporter gene, we identified a noncardiomyocyte cell population affected by alphaMHC-driven gene recombination localized to these tissue compartments at baseline. These cells were found to be cardiac progenitor cells since they coexpressed markers of proliferation (Ki67) and the cardiomyocyte lineage (alphaMHC, GATA4, Tbx5) but not cardiac Troponin T (cTnT). The cell population overlaps in part with both the previously described c-kit(pos) and stem cell antigen-1 (Sca-1)(pos) precursor cell population but not with the Islet-1(pos) precursor cell pool. An in vitro coculture assay of highly enriched (>95%) Sca-1(pos) cardiac precursor cells from beta-catenin-depleted mice compared to cells isolated from control littermate demonstrated increased differentiation toward alpha-actin(pos) and cTnT(pos) cardiomyocytes after 10 days (CT(Deltaex3-6): 38.0 +/- 1.0% alpha-actin(pos); beta-cat(Deltaex3-6): 49.9 +/- 2.4% alpha-actin(pos), P < 0.001). We conclude that beta-catenin depletion attenuates postinfarct LV remodeling in part through increased differentiation of GATA4(pos)/Sca-1(pos) resident cardiac progenitor cells.
Keywords:Cell Differentiation, Cell Proliferation, Down-Regulation, Reporter Genes, Cardiac Myoblasts, Myocardial Infarction, Regeneration, Ventricular Remodeling, beta Catenin, beta-Galactosidase, Animals, Mice
Source:Proceedings of the National Academy of Sciences of the United States of America
ISSN:0027-8424
Publisher:National Academy of Sciences (U.S.A.)
Volume:105
Number:50
Page Range:19762-19767
Date:16 December 2008
Official Publication:https://doi.org/10.1073/pnas.0808393105
PubMed:View item in PubMed

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