Differentiation of human embryonic stem cells into smooth muscle cells in adherent monolayer culture.

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Citation

Huang H, Zhao X, Chen L, Xu C, Yao X, Lu Y, Dai L, Zhang M

Differentiation of human embryonic stem cells into smooth muscle cells in adherent monolayer culture.

Biochem Biophys Res Commun. 2006 Dec 15;351(2):321-7. Epub 2006 Oct 17.

PubMed ID
17069765 [ View in PubMed
]
Abstract

Smooth muscle cell (SMC) plays critical roles in many human diseases, an in vitro system that recapitulates human SMC differentiation would be invaluable for exploring molecular mechanisms leading to the human diseases. We report a directed and highly efficient SMC differentiation system by treating the monolayer-cultivated human embryonic stem cells (hESCs) with all-trans retinoid acid (atRA). When the hESCs were cultivated in differentiation medium containing 10microM RA, more than 93% of the cells expressed SMC-marker genes along with the steadily accumulation of such SMC-specific proteins as SM alpha-actin and SM-MHC. The fully differentiated SMCs were stable in phenotype and capable of contraction. This inducible and highly efficient in vitro human SMC system could be an important resource to study the mechanisms of SMC phenotype determination in human.