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c-kit Is Required for Cardiomyocyte Terminal Differentiation.

c-kit Is Required for Cardiomyocyte Terminal Differentiation. Research Abstract Details 

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  • c-kit Is Required for Cardiomyocyte Terminal Differentiation. Abstract Text:

    ming liMing Li,nawazish naqviNawazish Naqvi,eiji yahiroEiji Yahiro,ke liuKe Liu,pamela c powellPamela C Powell,wayne e bradleyWayne E Bradley,david i k martinDavid I K Martin,robert m grahamRobert M Graham,louis j dell'italiaLouis J Dell'italia,ahsan husainAhsan Husain,ming liMing Li,nawazish naqviNawazish Naqvi,eiji yahiroEiji Yahiro,ke liuKe Liu,pamela c powellPamela C Powell,wayne e bradleyWayne E Bradley,david i k martinDavid I K Martin,robert m grahamRobert M Graham,louis j dell'italiaLouis J Dell'Italia,ahsan husainAhsan Husain,

    c-kit, the transmembrane tyrosine kinase receptor for stem cell factor, is required for melanocyte and mast cell development, hematopoiesis, and differentiation of spermatogonial stem cells. We show here that in the heart, c-kit is expressed not only by cardiac stem cells but also by cardiomyocytes, commencing immediately after birth and terminating a few days later, coincident with the onset of cardiomyocyte terminal differentiation. To examine the function of c-kit in cardiomyocyte terminal differentiation, we used compound heterozygous mice carrying the W (null) and W(v) (dominant negative) mutations of c-kit. In vivo, adult W/W(v) cardiomyocytes are phenotypically indistinguishable from their wild-type counterparts. After acute pressure overload adult W/W(v) cardiomyocytes reenter the cell cycle and proliferate, leading to left ventricular growth; furthermore in transgenic mice with cardiomyocyte-restricted overexpression of the dominant negative W(v) mutant, pressure overload causes cardiomyocytes to reenter the cell cycle. In contrast, in wild-type mice left ventricular growth after pressure overload results mainly from cardiomyocyte hypertrophy. Importantly, W/W(v) mice with pressure overload-induced cardiomyocyte hyperplasia had improved left ventricular function and survival. In W/W(v) mice, c-kit dysfunction also resulted in an approximately 14-fold decrease (P<0.01) in the number of c-kit(+)/GATA4(+) cardiac progenitors. These findings identify novel functions for c-kit: promotion of cardiac stem cell differentiation and regulation of cardiomyocyte terminal differentiation.

    c-kit Is Required for Cardiomyocyte Terminal Differentiation. Publishing Authors By Initials

    m liM Li,n naqviN Naqvi,e yahiroE Yahiro,k liuK Liu,pc powellPC Powell,we bradleyWE Bradley,di martinDI Martin,rm grahamRM Graham,lj dell'italiaLJ Dell'italia,a husainA Husain,m liM Li,n naqviN Naqvi,e yahiroE Yahiro,k liuK Liu,pc powellPC Powell,we bradleyWE Bradley,di martinDI Martin,rm grahamRM Graham,lj dell'italiaLJ Dell'Italia,a husainA Husain,

    For similar abstracts research abstracts see: abstracts research

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    c-kit Is Required for Cardiomyocyte Terminal Differentiation. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Circulation research

    VOLUME: 102

    Page Numbers: 677-85

    Journal Abbreviation: Circ. Res.

    ISSN: 1524-4571

    DAY: 7

    MONTH: 02

    YEAR: 2008

    c-kit Is Required for Cardiomyocyte Terminal Differentiation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 47103

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    Grant and Affiliation Information for c-kit Is Required for Cardiomyocyte Terminal Differentiation.

    AFFILIATION: University of Alabama at Birmingham, BMR2-435, 901 19th St S, Birmingham, AL 35294. ahusain@physiology.uab.edu.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Circ Res

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