The role of CTGF in diabetic retinopathy

被引:88
作者
Klaassen, Ingeborg [1 ,2 ]
van Geest, Rob J. [1 ,2 ]
Kuiper, Esther J. [1 ,2 ]
van Noorden, Cornelis J. F. [1 ,2 ]
Schlingemann, Reinier O. [1 ,2 ,3 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Ophthalmol, Ocular Angiogenesis Grp, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
[3] Royal Acad Sci, Netherlands Inst Neurosci, Amsterdam, Netherlands
关键词
Connective tissue growth factor; Pre-clinical diabetic retinopathy; Proliferative diabetic retinopathy; Extracellular matrix; Basal lamina thickening; Wound healing; Angio-fibrotic switch; TISSUE GROWTH-FACTOR; GLYCATION END-PRODUCTS; ACTIVATOR INHIBITOR TYPE-1; BASEMENT-MEMBRANE; FACTOR-BETA; GENE-EXPRESSION; EXTRACELLULAR-MATRIX; CCN FAMILY; INTRAVITREAL BEVACIZUMAB; DOWN-REGULATION;
D O I
10.1016/j.exer.2014.10.016
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Connective tissue growth factor (CTGF, CCN2) contributes to fibrotic responses in diabetic retinopathy, both before clinical manifestations occur in the pre-clinical stage of diabetic retinopathy (PCDR) and in proliferative diabetic retinopathy (PDR), the late clinical stage of the disease. CTGF is a secreted protein that modulates the actions of many growth factors and extracellular matrix (ECM) proteins, leading to tissue reorganization, such as ECM formation and remodeling, basal lamina (BL) thickening, pericyte apoptosis, angiogenesis, wound healing and fibrosis. In PCDR, CTGF contributes to thickening of the retinal capillary BL and is involved in loss of pericytes. In this stage, CTGF expression is induced by advanced glycation end products, and by growth factors such as vascular endothelial growth factor (VEGF) and transforming growth factor (TGF)-beta. In PDR, the switch from neovascularization to a fibrotic phase the angio-fibrotic switch in PDR is driven by CTGF, in a critical balance with vascular endothelial growth factor (VEGF). We discuss here the roles of CTGF in the pathogenesis of DR in relation to ECM remodeling and wound healing mechanisms, and explore whether CTGF may be a potential novel therapeutic target in the clinical management of early as well as late stages of DR. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:37 / 48
页数:12
相关论文
共 174 条
[61]   Matrix metalloproteinases cleave connective tissue growth factor and reactivate angiogenic activity of vascular endothelial growth factor 165 [J].
Hashimoto, G ;
Inoki, I ;
Fujii, Y ;
Aoki, T ;
Ikeda, E ;
Okada, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) :36288-36295
[62]   Connective tissue growth factor as a mediator of intraocular fibrosis [J].
He, Shikun ;
Chen, Youxin ;
Khankan, Rima ;
Barron, Ernesto ;
Burton, Richard ;
Zhu, DanHong ;
Ryan, Stephen J. ;
Oliver, Noelynn ;
Hinton, David R. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2008, 49 (09) :4078-4088
[63]   Hypoxic induction of Ctgf is directly mediated by Hif-1 [J].
Higgins, DF ;
Biju, MP ;
Akai, Y ;
Wutz, A ;
Johnson, RS ;
Haase, VH .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 287 (06) :F1223-F1232
[64]   Accumulation of NH2-terminal fragment of connective tissue growth factor in the vitreous of patients with proliferative diabetic retinopathy [J].
Hinton, DR ;
Spee, C ;
He, S ;
Weitz, S ;
Usinger, W ;
LaBree, L ;
Oliver, N ;
Lim, JI .
DIABETES CARE, 2004, 27 (03) :758-764
[65]   Novel growth factors involved in the pathogenesis of proliferative vitreoretinopathy [J].
Hinton, DR ;
He, S ;
Jin, ML ;
Barron, E ;
Ryan, SJ .
EYE, 2002, 16 (04) :422-428
[66]   Elevated aqueous humour tissue inhibitor of matrix metalloproteinase-1 and connective tissue growth factor in pseudoexfoliation syndrome [J].
Ho, SL ;
Dogar, GF ;
Wang, J ;
Crean, J ;
Wu, QD ;
Oliver, N ;
Weitz, S ;
Murray, A ;
Cleary, PE ;
O'Brien, C .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2005, 89 (02) :169-173
[67]   Acute contraction of the proliferative membrane after an intravitreal injection of bevacizumab for advanced retinopathy of prematurity [J].
Honda, Shigeru ;
Hirabayashi, Hiroaki ;
Tsukahara, Yasutomo ;
Negi, Akira .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2008, 246 (07) :1061-1063
[68]   CT domain of CCN2/CTGF directly interacts with fibronectin and enhances cell adhesion of chondrocytes through integrin α5β1 [J].
Hoshijima, M ;
Hattori, T ;
Inoue, M ;
Araki, D ;
Hanagata, H ;
Miyauchi, A ;
Takigawa, M .
FEBS LETTERS, 2006, 580 (05) :1376-1382
[69]   Intravitreal Injection of Ranibizumab and CTGF shRNA Improves Retinal Gene Expression and Microvessel Ultrastructure in a Rodent Model of Diabetes [J].
Hu, Bojie ;
Zhang, Yan ;
Zeng, Qing ;
Han, Qian ;
Zhang, Lijuan ;
Liu, Mian ;
Li, Xiaorong .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (01) :1606-1624
[70]   Advanced glycation end products cause increased CCN family and extracellular matrix gene expression in the diabetic rodent retina [J].
Hughes, J. M. ;
Kuiper, E. J. ;
Klaassen, I. ;
Canning, P. ;
Stitt, A. W. ;
Van Bezu, J. ;
Schalkwijk, C. G. ;
Van Noorden, C. J. F. ;
Schlingemann, R. O. .
DIABETOLOGIA, 2007, 50 (05) :1089-1098