BMP-2 and TGFβ2 shared pathways regulate endocardial cell transformation

Todd A. Townsend, Jamille Y. Robinson, Christopher R. Deig, Cynthia R. Hill, Andrew Misfeldt, Gerard C. Blobe, Joey V. Barnett

Research output: Contribution to journalArticlepeer-review

28 Scopus citations


Valvular heart disease is a major cause of mortality and morbidity. Revealing the cellular processes and molecules that regulate valve formation and remodeling is required to develop effective therapies. A key step in valve formation during heart development is the epithelial-mesenchymal transformation (EMT) of a subpopulation of endocardial cells in the atrioventricular cushion (AVC). The type III transforming growth factor-β receptor (TGFβR3) regulates AVC endocardial cell EMT in vitro and mesenchymal cell differentiation in vivo. Little is known concerning the signaling mechanisms downstream of TGFβR3. Here we use endocardial cell EMT in vitro to determine the role of 2 well-characterized downstream TGFβ signaling pathways in TGFβR3-dependent endocardial cell EMT. Targeting of Smad4, the common mediator Smad, demonstrated that Smad signaling is required for EMT in the AVC and TGFβR3-dependent EMT stimulated by TGFβ2 or BMP-2. Although we show that Smads 1, 2, 3, and 5 are required for AVC EMT, overexpression of Smad1 or Smad3 is not sufficient to induce EMT. Consistent with the activation of the Par6/Smurf1 pathway downstream of TGFβR3, targeting ALK5, Par6, or Smurf1 significantly inhibited EMT in response to either TGFβ2 or BMP-2. The requirement for ALK5 activity, Par6, and Smurf1 for TGFβR3-dependent endocardial cell EMT is consistent with the documented role of this pathway in the dissolution of tight junctions. Taken together, our data demonstrate that TGFβR3-dependent endocardial cell EMT stimulated by either TGFβ2 or BMP-2 requires Smad4 and the activation of the Par6/Smurf1 pathway.

Original languageEnglish
Pages (from-to)1-12
Number of pages12
JournalCells Tissues Organs
Issue number1
StatePublished - Jun 2011


  • Atrioventricular cushion
  • Epithelial mesenchymal transformation
  • Heart valve
  • Receptors
  • Transforming growth factor-β


Dive into the research topics of 'BMP-2 and TGFβ2 shared pathways regulate endocardial cell transformation'. Together they form a unique fingerprint.

Cite this