期刊文献+

BIGH3基因在角膜疾病及糖尿病视网膜病变中的研究新进展 被引量:3

Latest progress of BIGH3 gene in corneal diseases and diabetic retinopat hy
下载PDF
导出
摘要 BIGH3基因在眼部疾病中起重要作用。一方面,与角膜疾病的发生息息相关,BIGH3基因可以抑制角膜新生血管形成,导致角膜营养不良,参与圆锥角膜形成;另一方面,可以导致糖尿病视网膜病变中新生血管的生成,有最新实验证明,巨噬细胞分泌的TGFβ可以促进BIGH3 mRNA和BIGH3蛋白的表达,并促进视网膜内皮细胞和周细胞凋亡,从而导致糖尿病视网膜病变新生血管的形成。本文将从如上几个方面阐述BIGH3基因在眼部疾病研究的新进展。 BIGH3 gene plays an important role in ocular diseases.On the one hand,it is closely related to the occurrence of corneal diseases.BIGH3 gene can inhibit corneal neovascularization,lead to corneal dystrophy,participate in keratoconus formation.On the other hand,it can lead to the formation of neovascularization in diabetic retinopathy.The latest experiments show that TGF beta secreted by macrophages can promote the expression of BIGH3 mRNA and BIGH3 protein,and promote apoptosis of retinal endothelial cells and pericytes,which leads to the formation of neovascularization in diabetic retinopathy.This article will describe the new progress of BIGH3 gene in ocular diseases from several aspects as mentioned above.
出处 《国际眼科杂志》 CAS 2017年第3期449-450,共2页 International Eye Science
基金 国家自然科学青年基金项目(No.81300728) 黑龙江省教育厅面上项目(No.12541516)~~
关键词 BIGH3 角膜新生血管 角膜营养不良 圆锥角膜 糖尿病视网膜病变 BIGH3 corneal neovascularization corneal dystrophy keratoconus diabetic retinopathy
  • 相关文献

参考文献3

二级参考文献146

  • 1王旭,张华,张玉光,韩旭光,张磊,李廷军.圆锥角膜患者房水中sFas、sFasL质量浓度的变化[J].眼科研究,2005,23(5):510-512. 被引量:1
  • 2Rabinowitz YS. Keratoconus[ J ]. Surv Ophthahnol, 1998,42 ( 4 ) : 297-319. 被引量:1
  • 3lncorvaia C, Parmeggiani F, Costagliola C,et al. Congenital adrenal hyperplasia due to 21 hydroxylased eficiency assoeiated with bilateral keratoconus[J]. Am J Ophthahnol,2003,155 ( 4 ) :557-559. 被引量:1
  • 4Ambrosio RJ, Klyee SD, Wilson SE. Corneal topographic and pachymetric screening of keratorefractive patients [ J ]. J Refrat Surg,2003,19( 1 ) :24-29. 被引量:1
  • 5Tyynismaa H ,Sistonen P,Tuupanen S,et al. A locus for autosomal dominant keratoconus:linkage to 16q22.3-q23.1 in Finnish families [J]. Invest Ophthahnol Vis Sci, 2002,43 ( 10 ) : 3160 -3164. 被引量:1
  • 6Hughes AE, Dash DP,Jackson AJ,et al. Familial kerataconus with cataract :linkage to the long arm of chromsome 15 and exclusion of candidate genes [ J ]. Invest ophthahnol Vis Sci, 2003,44 ( 12 ) : 5063-5066. 被引量:1
  • 7Brancati F, Valente EM, Sarkazy A, et al. A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13 [ J ]. Med Genet ,2004,41 ( 3 ) : 188-192. 被引量:1
  • 8Rabinowitz RS, Dong L,Wistow G. Gene expression profile studies of human keratoconus cornea for NEI Bank:a novel cornea-expressed gene and the absence of transcripts for aquaporin 5 [ J ]. Invest Ophthahnol Vis Sci, 2005,46 ( 4 ) : 1239-1246. 被引量:1
  • 9Garfias A,Navas A, P6rez-Cano HJ, et al. Comparative expression analysis of aquaporin-5 ( AQP5 ) in keratoconic and healthy corneas [ J]. Mol Vis,2008,14:756-761. 被引量:1
  • 10He'on E, Greenberg A, Kopp KK,et al. VSXI :a gene for posterior polymorphous dystrophy and keratoconus [ J]. Hum Mol Genet, 2002,11(9) :1029-1036. 被引量:1

共引文献5

同被引文献39

引证文献3

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部