4.4 Article

Cell Autonomous Requirement of Endocardial Smad4 During Atrioventricular Cushion Development in Mouse Embryos

Journal

DEVELOPMENTAL DYNAMICS
Volume 240, Issue 1, Pages 211-220

Publisher

WILEY
DOI: 10.1002/dvdy.22493

Keywords

valvulogenesis; BMP; Smad4; congenital heart disease; atrioventricular cushion

Funding

  1. American Heart Association [0535177N, 09GRNT2060268]
  2. NHBLI [R01HL095783, R01HL095783-01A1]
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL095783] Funding Source: NIH RePORTER

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Atrioventricular (AV) cushions are the precursors of AV septum and valves. In this study, we examined roles of Smad4 during AV cushion development using a conditional gene inactivation approach. We found that endothelial/endocardial inactivation of Smad4 led to the hypocellular AV cushion defect and that both reduced cell proliferation and increased apoptosis contributed to the defect. Expression of multiple genes critical for cushion development was down-regulated in mutant embryos. In collagen gel assays, the number of mesenchymal cells formed is significantly reduced in mutant AV explants compared to that in control explants, suggesting that the reduction of cushion mesenchyme formation in mutants is unlikely secondary to their gross vasculature abnormalities. Using a previously developed immortal endocardial cell line, we showed that Smad4 is required for BMP signaling-stimulated upregulation of Tbx20 and Gata4. Therefore, our data collectively support the cell-autonomous requirement of endocardial Smad4 in regulating AV cushion development. Developmental Dynamics 240: 211-220, 2011. (C) 2010 Wiley-Liss, Inc.

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