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The inhibition of the effect and mechanism of vascular intimal hyperplasia in Tiam1 knockout mice.
Kou, Wenxin; Xu, Xu; Ji, Shuya; Chen, Mengyao; Liu, Dongdong; Wang, Kai; Zhuang, Jianhui; Yu, Qing; Zhao, Qian; Xu, Yawei; Zhang, Hongli; Peng, Wenhui.
Afiliação
  • Kou W; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Xu X; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Ji S; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Chen M; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Liu D; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Wang K; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Zhuang J; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Yu Q; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Zhao Q; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Xu Y; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Zhang H; Department of Endocrinology, Seventh People's Hospital of Shanghai University of TCM, Shanghai, China. Electronic address: hongliting@sina.com.
  • Peng W; Department of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China. Electronic address: pwenhui@tongji.edu.cn.
Biochem Biophys Res Commun ; 497(1): 248-255, 2018 02 26.
Article em En | MEDLINE | ID: mdl-29432743
ABSTRACT
T-Cell Lymphoma Invasion and Metastasis 1 (Tiam1) is a specific nucleotide exchange factor (GEF) that can activate Rho-like GTPase and Rac1 and regulate various cellular processes, including cell cycle progression and cell migration. The roles of Tiam1 in vascular intimal hyperplasia, especially in vascular smooth muscle cell proliferation and migration, are not fully understood. In this study, we investigated the effect of Tiam1 on vascular intimal hyperplasia in a carotid artery ligation model and human aortic smooth muscle cells (HASMCs). We found that the expression of Tiam1 was up-regulated in the neointima of carotid artery ligation mice and that Tiam1-/- mice following carotid artery ligation had less neointimal formation compared with wild type mice. Knockdown of Tiam1 by siRNA markedly attenuated PDGF-induced migration and proliferation in HASMCs by inhibiting the activation of Rac1. Therefore, these results suggest that Tiam1 is an important regulator of intima hyperplasia. It may regulate vascular intimal hyperplasia through the activation of Rac1.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Túnica Íntima / Miócitos de Músculo Liso / Músculo Liso Vascular Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Túnica Íntima / Miócitos de Músculo Liso / Músculo Liso Vascular Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China