The role of ERK and JNK signaling in connective tissue growth factor induced extracellular matrix protein production and scar formation

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• 作者：Xiaolong Hu (1)
  Hongtao Wang (1)
  Jiaqi Liu (1)
  Xiaobing Fang (1)
  Ke Tao (1)
  Yaojun Wang (1)
  Na Li (1)
  Jihong Shi (1)
  Yunchuan Wang (1)
  Peng Ji (1)
  Weixia Cai (1)
  Xiaozhi Bai (1)
  Xiongxiang Zhu (1)
  Juntao Han (1)
  Dahai Hu (1)
  
• 关键词：Hypertrophic scar ; Extracellular signal ; regulated kinase ; c ; Jun N ; terminal kinase ; Connective tissue growth factor ; Scar formation
• 刊名：Archives of Dermatological Research
• 出版年：2013
• 出版时间：July 2013
• 年：2013
• 卷：305
• 期：5
• 页码：433-445
• 全文大小：2547KB
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• 作者单位：Xiaolong Hu (1)
  Hongtao Wang (1)
  Jiaqi Liu (1)
  Xiaobing Fang (1)
  Ke Tao (1)
  Yaojun Wang (1)
  Na Li (1)
  Jihong Shi (1)
  Yunchuan Wang (1)
  Peng Ji (1)
  Weixia Cai (1)
  Xiaozhi Bai (1)
  Xiongxiang Zhu (1)
  Juntao Han (1)
  Dahai Hu (1)
  
  1. Department of Burns and Cutaneous Surgery, Xijing Hospital, Fourth Military Medical University, 127 Changle West Road, Xi’an, 710032, Shaanxi, China
  
• ISSN：1432-069X

文摘

CCN2 plays an important role in the pathogenesis of hypertrophic scars (HTSs). Although CCN2 is involved in many fibroproliferative events, the CCN2 induction signaling pathway in HTSs is yet to be elucidated. Here, we first investigated the effect of the mitogen-activated protein kinases (MAPKs) on CCN2-induced α-smooth muscle actin (α-SMA) and collagen I expression in human HTS fibroblasts (HTSFs). Then, we established HTSs in a rabbit ear model and determined the effect of MAPKs on the pathogenesis of HTSs. MAPK pathways were activated by CCN2 in HTSFs. Extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK) inhibitors significantly inhibited CCN2-induced expression of α-SMA and collagen I in HTSFs. In the rabbit ear model of the HTS, JNK and ERK inhibitors significantly improved the architecture of the rabbit ear scar and reduced scar formation on the rabbit ear. Our results indicate that ERK and JNK mediate collagen I expression and scarring of the rabbit ear, and may be considered for specific drug therapy targets for HTSs.