圆锥角膜
免疫组织化学
免疫球蛋白轻链
自噬
生物
发病机制
染色
细胞生物学
病理
角膜
眼科
医学
抗体
免疫学
遗传学
细胞凋亡
作者
Omer Iqbal,G. H. Fisher,Samir Vira,Daneyal Syed,Nasir Sadeghi,David W. Freeman,Edward M. Campbell,Joel Sugar,Robert Feder,Jawed Fareed,Charles S. Bouchard
出处
期刊:Cornea
[Lippincott Williams & Wilkins]
日期:2013-02-27
卷期号:32 (5): 702-707
被引量:17
标识
DOI:10.1097/ico.0b013e318282987a
摘要
Purpose: To study the expression of secreted frizzled-related protein-1 (SFRP-1) and microtubule-associated protein light chain 3 (LC3), an autophagy marker, in keratoconus. Methods: Under an institutional review board–approved protocol, de-identified and/or surgically discarded normal donor (n = 10) and keratoconus corneas (n = 10) were obtained. The corneal samples were fixed in formalin and embedded in paraffin. Immunohistochemical staining using SFRP-1 and LC3 antibodies was performed. Results: The majority of expression of SFRP-1 was seen in the epithelium; however, in 3 tissues that showed high expression, staining was also present in the stroma and endothelium. Like SFRP-1, the LC3 expression in keratoconus tissues occurred at 3 different levels: low, medium, and high. Collectively these data suggest that there are differences in the expression levels of SFRP-1 and LC3 in keratoconus tissue compared with the normal tissue. Low expressivity of SFRP-1 seemed to correspond to low expressivity of LC3, whereas medium to high expressivity of SFRP-1 corresponded to medium to high expressivity of LC3. Conclusions: Increased expression of SFRP-1 and LC3 was observed in keratoconus corneas. Keratocyte autophagy seen with keratoconus may play a role in the pathogenesis of keratoconus.
科研通智能强力驱动
Strongly Powered by AbleSci AI