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Cyclic strain induces mouse embryonic stem cell differentiation into vascular smooth muscle cells by activating PDGF receptor β

¹Department of Biomedical Engineering and ²Department of Pediatrics, Graduate School of Medicine, University of Tokyo, Tokyo, Japan; ³PRESTO, Japan Science and Technology Agency, Saitama, Japan; ⁴Department of Cardiovascular Physiology, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Japan; ⁵Stem Cell Research Center, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan

Submitted 13 August 2007 ; accepted in final form 22 December 2007

Embryonic stem (ES) cells are exposed to fluid-mechanical forces, such as cyclic strain and shear stress, during the process of embryonic development but much remains to be elucidated concerning the role of fluid-mechanical forces in ES cell differentiation. Here, we show that cyclic strain induces vascular smooth muscle cell (VSMC) differentiation in murine ES cells. Flk-1-positive (Flk-1⁺) ES cells seeded on flexible silicone membranes were subjected to controlled levels of cyclic strain and examined for changes in cell proliferation and expression of various cell lineage markers. When exposed to cyclic strain (4–12% strain, 1 Hz, 24 h), the Flk-1⁺ ES cells significantly increased in cell number and became oriented perpendicular to the direction of strain. There were dose-dependent increases in the VSMC markers smooth muscle -actin and smooth muscle-myosin heavy chain at both the protein and gene expression level in response to cyclic strain, whereas expression of the vascular endothelial cell marker Flk-1 decreased, and there were no changes in the other endothelial cell markers (Flt-1, VE-cadherin, and platelet endothelial cell adhesion molecule 1), the blood cell marker CD3, or the epithelial marker keratin. The PDGF receptor β (PDGFRβ) kinase inhibitor AG-1296 completely blocked the cyclic strain-induced increase in cell number and VSMC marker expression. Cyclic strain immediately caused phosphorylation of PDGFRβ in a dose-dependent manner, but neutralizing antibody against PDGF-BB did not block the PDGFRβ phosphorylation. These results suggest that cyclic strain activates PDGFRβ in a ligand-independent manner and that the activation plays a critical role in VSMC differentiation from Flk-1⁺ ES cells.

hemodynamic force; biomechanics; blood vessel

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