Hippo signaling determines the number of venous pole cells that originate from the anterior lateral plate mesoderm in zebrafish

Elife. 2018 May 29:7:e29106. doi: 10.7554/eLife.29106.

Abstract

The differentiation of the lateral plate mesoderm cells into heart field cells constitutes a critical step in the development of cardiac tissue and the genesis of functional cardiomyocytes. Hippo signaling controls cardiomyocyte proliferation, but the role of Hippo signaling during early cardiogenesis remains unclear. Here, we show that Hippo signaling regulates atrial cell number by specifying the developmental potential of cells within the anterior lateral plate mesoderm (ALPM), which are incorporated into the venous pole of the heart tube and ultimately into the atrium of the heart. We demonstrate that Hippo signaling acts through large tumor suppressor kinase 1/2 to modulate BMP signaling and the expression of hand2, a key transcription factor that is involved in the differentiation of atrial cardiomyocytes. Collectively, these results demonstrate that Hippo signaling defines venous pole cardiomyocyte number by modulating both the number and the identity of the ALPM cells that will populate the atrium of the heart.

Keywords: Hippo; Lats kinase; Yap; cardiogenesis; developmental biology; heart field; islet-1; stem cells; zebrafish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Bone Morphogenetic Proteins / genetics
  • Bone Morphogenetic Proteins / metabolism
  • Cell Count
  • Cell Differentiation
  • Cell Proliferation
  • Embryo, Nonmammalian
  • Gene Expression Regulation, Developmental
  • Heart Atria / cytology
  • Heart Atria / growth & development
  • Heart Atria / metabolism*
  • Mesoderm / cytology
  • Mesoderm / growth & development
  • Mesoderm / metabolism*
  • Myocardium / cytology
  • Myocardium / metabolism
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / metabolism*
  • Organogenesis / genetics
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Serine-Threonine Kinase 3
  • Signal Transduction / genetics*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism
  • Zebrafish
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Bone Morphogenetic Proteins
  • Tumor Suppressor Proteins
  • Zebrafish Proteins
  • hand2 protein, zebrafish
  • Protein Serine-Threonine Kinases
  • Serine-Threonine Kinase 3
  • stk3 protein, zebrafish

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.