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视黄醇结合蛋白4在糖尿病视网膜病变发病机制中的作用

李鹏伟 高永峰   

  1. 450003 郑州大学人民医院眼科
  • 收稿日期:2017-11-22 出版日期:2018-02-22 发布日期:2018-03-08
  • 通讯作者: 高永峰,Email:gaoyf13@163.com E-mail:gaoyf13@163.com

Role of retinol binding protein 4 in pathogenesis of diabetic retinopathy

LI Peng-wei, GAO Yong-feng   

  1. Department of Ophthalmology,  People's Hospital affliated to Zhengzhou University,Zhengzhou 450003,China
  • Received:2017-11-22 Online:2018-02-22 Published:2018-03-08
  • Contact: GAO Yong-feng, Email: gaoyf13@163.com E-mail:gaoyf13@163.com

摘要:

糖尿病视网膜病变(diabetic retinopathy,DR)是2型糖尿病(type 2 diabetes mellitus,T2DM)的主要并发症,是造成视力损害和可预防盲的主要原因。炎症在T2DM和DR发病机制中起着至关重要的作用。视黄醇结合蛋白4(retinol binding protein 4,RBP4)是一种新的脂肪细胞因子,可通过Toll样受体4(TLR4)、c-Jun氨基端激酶(JNK)、细胞外信号调节激酶(ERK)、p38信号通路和核因子-κB (NF-κB)途径等促炎机制诱导抗原提呈和Th1细胞极化,导致胰岛素抵抗,从而间接导致T2DM和DR;而RBP4升高也可通过炎症机制直接导致视网膜血管内皮和神经炎症。此外,血清甲状腺素转运蛋白可能抑制RBP4诱导的视网膜内皮细胞的炎症。

Abstract:

Diabetic retinopathy (DR) is the main complication of type 2 diabetes mellitus (T2DM), and is the main cause of visual impairment and preventable blindness. It is well known that inflammation plays an important role in the pathogenesis of T2DM and DR. Retinol binding protein 4 (RBP4) is a novel adipocyte factor, which can induce the insulin resistance and retinal degeneration indirectly through proinflammatory mechanisms, such as Toll like receptor 4 (TLR4), c-Jun amino terminal kinase (JNK), extracellular signal regulated kinase (ERK), p38 signaling pathway, and nuclear factor kappa B (NF-κB), etc. Also the rise of RBP4 can induce insulin resistance and retinal degeneration directly through inflammatory mechanism. In addition, the serum transthyretin (TTR) might inhibit the inflammation of retinal endothelial cells induced by RBP4.