Key result
Leupaxin induces smooth muscle gene expression by acting as a serum response factor cofactor.
Leupaxin functions as a serum response factor cofactor to induce smooth muscle cell gene transcription, providing a mechanism by which extracellular matrix signals regulate smooth muscle phenotypic switching.
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Should not yet change practice; extends mechanistic understanding of smooth muscle gene regulation in animal models.
Leupaxin is a LIM domain-containing adapter protein belonging to the paxillin family that has been previously reported to be preferentially expressed in hematopoietic cells. Herein, we identified leupaxin in a screen for focal adhesion kinase binding partners in aortic smooth muscle, and we show that leupaxin is enriched in human and mouse vascular smooth muscle and that leupaxin expression is dynamically regulated during development. In addition, our studies reveal that leupaxin can undergo cytoplasmic/nuclear shuttling and functions as an serum response factor cofactor in the nucleus. We found that leupaxin forms a complex with serum response factor and associates with CArG-containing regions of smooth muscle promoters and that ectopic expression of leupaxin induces smooth muscle marker gene expression in both 10T1/2 cells and rat aortic smooth muscle cells. Subsequent studies indicated that enhanced focal adhesion kinase activity (induced by fibronectin or expression of constitutively active focal adhesion kinase) attenuates the nuclear accumulation of leupaxin and limits the ability of leupaxin to enhance serum response factor-dependent gene transcription. Thus, these studies indicate that modulation of the subcellular localization of serum response factor cofactors is 1 mechanism by which extracellular matrix-dependent signals may regulate phenotypic switching of smooth muscle cells.
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Sundberg-Smith et al. (2008) studied this question. Leupaxin expression was evaluated on Smooth muscle marker gene expression. Leupaxin is enriched in vascular smooth muscle, undergoes cytoplasmic/nuclear shuttling, and functions as a serum response factor cofactor to induce smooth muscle marker gene expression.
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