J. Dev. Biol. 2013, 1(2), 159-185; doi:10.3390/jdb1020159
Article

Soluble VCAM-1 Alters Lipid Phosphatase Activity in Epicardial Mesothelial Cells: Implications for Lipid Signaling During Epicardial Formation

Received: 2 May 2013; in revised form: 12 July 2013 / Accepted: 23 August 2013 / Published: 18 September 2013
(This article belongs to the Special Issue Epicardial Development and Cardiovascular Disease)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Epicardial formation involves the attachment of proepicardial (PE) cells to the heart and the superficial migration of mesothelial cells over the surface of the heart. Superficial migration has long been known to involve the interaction of integrins expressed by the epicardium and their ligands expressed by the myocardium; however, little is understood about signals that maintain the mesothelium as it migrates. One signaling pathway known to regulate junctional contacts in epithelia is the PI3K/Akt signaling pathway and this pathway can be modified by integrins. Here, we tested the hypothesis that the myocardially expressed, integrin ligand VCAM-1 modulates the activity of the PI3K/Akt signaling pathway by activating the lipid phosphatase activity of PTEN. We found that epicardial cells stimulated with a soluble form of VCAM-1 (sVCAM-1) reorganized PTEN from the cytoplasm to the membrane and nucleus and activated PTEN’s lipid phosphatase activity. Chick embryonic epicardial mesothelial cells (EMCs) expressing a shRNA to PTEN increased invasion in collagen gels, but only after stimulation by TGFβ3, indicating that loss of PTEN is not sufficient to induce invasion. Expression of an activated form of PTEN was capable of blocking degradation of junctional complexes by TGFβ3. This suggested that PTEN plays a role in maintaining the mesothelial state of epicardium and not in EMT. We tested if altering PTEN activity could affect coronary vessel development and observed that embryonic chick hearts infected with a virus expressing activated human PTEN had fewer coronary vessels. Our data support a role for VCAM-1 in mediating critical steps in epicardial development through PTEN in epicardial cells.
Keywords: CD106/VCAM-1; epicardium; PTEN; phosphatidylinositol phosphate; PIP2
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MDPI and ACS Style

Ranganathan, M.; Dokic, D.; Sterrett, S.W.; Dwyer, K.L.; Dettman, R.W. Soluble VCAM-1 Alters Lipid Phosphatase Activity in Epicardial Mesothelial Cells: Implications for Lipid Signaling During Epicardial Formation. J. Dev. Biol. 2013, 1, 159-185.

AMA Style

Ranganathan M, Dokic D, Sterrett SW, Dwyer KL, Dettman RW. Soluble VCAM-1 Alters Lipid Phosphatase Activity in Epicardial Mesothelial Cells: Implications for Lipid Signaling During Epicardial Formation. Journal of Developmental Biology. 2013; 1(2):159-185.

Chicago/Turabian Style

Ranganathan, Manjari; Dokic, Danijela; Sterrett, Sonia W.; Dwyer, Kathryn L.; Dettman, Robert W. 2013. "Soluble VCAM-1 Alters Lipid Phosphatase Activity in Epicardial Mesothelial Cells: Implications for Lipid Signaling During Epicardial Formation." J. Dev. Biol. 1, no. 2: 159-185.

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