Hand2 Loss-of-Function in Hand1 -Expressing Cells Reveals Distinct Roles in Epicardial and Coronary Vessel Development

Author:

Barnes Ralston M.1,Firulli Beth A.1,VanDusen Nathan J.1,Morikawa Yuka1,Conway Simon J.1,Cserjesi Peter1,Vincentz Joshua W.1,Firulli Anthony B.1

Affiliation:

1. From the Riley Heart Research Center (R.M.B., B.A.F., N.J.V., S.J.C., J.W.V., A.B.F.), Wells Center for Pediatric Research, Division of Pediatric Cardiology, Departments of Anatomy and Medical and Molecular Genetics, Indiana Medical School, Indianapolis; Department of Cell and Molecular Biology (Y.M.), Tulane University, New Orleans, LA; and Department of Pathology and Cell Biology (P.C.), Columbia University, New York.

Abstract

Rationale: The basic helix–loop–helix (bHLH) transcription factors Hand1 and Hand2 are essential for embryonic development. Given their requirement for cardiogenesis, it is imperative to determine their impact on cardiovascular function. Objective: To deduce the role of Hand2 within the epicardium. Method and Results: We engineered a Hand1 allele expressing Cre recombinase. Cardiac Hand1 expression is largely limited to cells of the primary heart field, overlapping little with Hand2 expression. Hand1 is expressed within the septum transversum, and the Hand1 lineage marks the proepicardial organ and epicardium. To examine Hand factor functional overlap, we conditionally deleted Hand2 from Hand1 -expressing cells. Hand2 mutants display defective epicardialization and fail to form coronary arteries, coincident with altered extracellular matrix deposition and Pdgfr expression. Conclusions: These data demonstrate a hierarchal relationship whereby transient Hand1 septum transversum expression defines epicardial precursors that are subsequently dependent on Hand2 function.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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