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Myocardium and BMP signaling are required for endocardial differentiation.

Publication ,  Journal Article
Palencia-Desai, S; Rost, MS; Schumacher, JA; Ton, QV; Craig, MP; Baltrunaite, K; Koenig, AL; Wang, J; Poss, KD; Chi, NC; Stainier, DYR; Sumanas, S
Published in: Development
July 1, 2015

Endocardial and myocardial progenitors originate in distinct regions of the anterior lateral plate mesoderm and migrate to the midline where they coalesce to form the cardiac tube. Endocardial progenitors acquire a molecular identity distinct from other vascular endothelial cells and initiate expression of specific genes such as nfatc1. Yet the molecular pathways and tissue interactions involved in establishing endocardial identity are poorly understood. The endocardium develops in tight association with cardiomyocytes. To test for a potential role of the myocardium in endocardial morphogenesis, we used two different zebrafish models deficient in cardiomyocytes: the hand2 mutant and a myocardial-specific genetic ablation method. We show that in hand2 mutants endocardial progenitors migrate to the midline but fail to assemble into a cardiac cone and do not express markers of differentiated endocardium. Endocardial differentiation defects were rescued by myocardial but not endocardial-specific expression of hand2. In metronidazole-treated myl7:nitroreductase embryos, myocardial cells were targeted for apoptosis, which resulted in the loss of endocardial nfatc1 expression. However, endocardial cells were present and retained expression of general vascular endothelial markers. We further identified bone morphogenetic protein (BMP) as a candidate myocardium-derived signal required for endocardial differentiation. Chemical and genetic inhibition of BMP signaling at the tailbud stage resulted in severe inhibition of endocardial differentiation while there was little effect on myocardial development. Heat-shock-induced bmp2b expression rescued endocardial nfatc1 expression in hand2 mutants and in myocardium-depleted embryos. Our results indicate that the myocardium is crucial for endocardial morphogenesis and differentiation, and identify BMP as a signal involved in endocardial differentiation.

Duke Scholars

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Published In

Development

DOI

EISSN

1477-9129

Publication Date

July 1, 2015

Volume

142

Issue

13

Start / End Page

2304 / 2315

Location

England

Related Subject Headings

  • Zebrafish Proteins
  • Zebrafish
  • Signal Transduction
  • NFATC Transcription Factors
  • Myocardium
  • Mutation
  • Models, Biological
  • Heat-Shock Response
  • Gene Deletion
  • Endocardium
 

Citation

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Palencia-Desai, S., Rost, M. S., Schumacher, J. A., Ton, Q. V., Craig, M. P., Baltrunaite, K., … Sumanas, S. (2015). Myocardium and BMP signaling are required for endocardial differentiation. Development, 142(13), 2304–2315. https://doi.org/10.1242/dev.118687
Palencia-Desai, Sharina, Megan S. Rost, Jennifer A. Schumacher, Quynh V. Ton, Michael P. Craig, Kristina Baltrunaite, Andrew L. Koenig, et al. “Myocardium and BMP signaling are required for endocardial differentiation.Development 142, no. 13 (July 1, 2015): 2304–15. https://doi.org/10.1242/dev.118687.
Palencia-Desai S, Rost MS, Schumacher JA, Ton QV, Craig MP, Baltrunaite K, et al. Myocardium and BMP signaling are required for endocardial differentiation. Development. 2015 Jul 1;142(13):2304–15.
Palencia-Desai, Sharina, et al. “Myocardium and BMP signaling are required for endocardial differentiation.Development, vol. 142, no. 13, July 2015, pp. 2304–15. Pubmed, doi:10.1242/dev.118687.
Palencia-Desai S, Rost MS, Schumacher JA, Ton QV, Craig MP, Baltrunaite K, Koenig AL, Wang J, Poss KD, Chi NC, Stainier DYR, Sumanas S. Myocardium and BMP signaling are required for endocardial differentiation. Development. 2015 Jul 1;142(13):2304–2315.
Journal cover image

Published In

Development

DOI

EISSN

1477-9129

Publication Date

July 1, 2015

Volume

142

Issue

13

Start / End Page

2304 / 2315

Location

England

Related Subject Headings

  • Zebrafish Proteins
  • Zebrafish
  • Signal Transduction
  • NFATC Transcription Factors
  • Myocardium
  • Mutation
  • Models, Biological
  • Heat-Shock Response
  • Gene Deletion
  • Endocardium