δEF1 Mediates TGF-β Signaling in Vascular Smooth Muscle Cell Differentiation

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• 作者：Go Nishimura ; Ichiro Manabe ; Kensuke Tsushima ; Katsuhito Fujiu ; Yumiko Oishi ; Yasushi Imai ; Koji Maemura ; Makoto Miyagishi ; Yujiro Higashi ; Hisato Kondoh ; Ryozo Nagai
• 关键词：CELLCYCLE
• 刊名：Developmental Cell
• 出版年：2006
• 出版时间：July 2006
• 年：2006
• 卷：11
• 期：1
• 页码：93-104
• 全文大小：778 K

文摘

Alteration in the differentiated state of smooth muscle cells (SMCs) is known to be integral to vascular development and the pathogenesis of vascular disease. However, it is still largely unknown how environmental cues translate into transcriptional control of SMC genes. We found that δEF1 is upregulated during SMC differentiation and selectively transactivates the promoters of SMC differentiation marker genes, SM α-actin and SM myosin heavy chain (SM-MHC). δEF1 physically interacts with SRF and Smad3, resulting in a synergistic activation of SM α-actin promoter. Chromatin immunoprecipitation assays and knockdown experiments showed that δEF1 is involved in the control of the SMC differentiation programs induced by TGF-β signaling. Overexpression of δEF1 inhibited neointima formation and promoted SMC differentiation, whereas heterozygous δEF1 knockout mice exhibited exaggerated neointima formation. It thus appears δEF1 mediates SMC differentiation via interaction with SRF and Smad3 during development and in vascular disease.