Institute for Wound Research, University of Florida, Gainesville, Florida, United States.
Invest Ophthalmol Vis Sci. 2014 Apr 1;55(4):2062-70. doi: 10.1167/iovs.13-12735.
This study aimed to elucidate the role of connective tissue growth factor (CTGF) in healthy eyes and wounded corneas of mice and rabbits. Conditional knockout mice were used to determine the role of CTGF in corneal healing.
CTGF expression was determined using transgenic mice carrying CTGF promoter driven-eGFP, quantitative RT-PCR, and immunofluorescent staining. Mice that carried two floxed CTGF alleles and a Cre/ERT2 transgene under the control of human ubiquitin C (ubc) promoter were used to conditionally delete CTGF gene in a tamoxifen-inducible manner. Phototherapeutic keratectomy (PTK) was used to generate an acute corneal wound and corneal re-epithelialization was assessed by fluorescein staining.
Connective tissue growth factor expression was found in multiple ocular tissues with relatively high levels in the corneal endothelium, lens subcapsular epithelium, and in the vasculature of the iris and retina. Wounded corneas responded with an immediate upregulation of CTGF in the epithelium at the wound margin and a sustained CTGF induction during re-epithelialization. At the onset of haze formation, CTGF protein becomes more focused in the basal epithelium. Deletion of the CTGF gene caused a 40% reduction (P < 0.01) in the cornea re-epithelialization rate in knockout mice compared with wild-type mice.
Connective tissue growth factor is expressed in the naïve cornea, lens, iris, and retina, and is expressed immediately after epithelial injury. Loss of CTGF impairs efficient re-epithelialization of corneal wounds.
本研究旨在阐明结缔组织生长因子(CTGF)在健康小鼠和兔眼以及受伤角膜中的作用。利用条件性敲除小鼠确定 CTGF 在角膜愈合中的作用。
利用携带 CTGF 启动子驱动的 eGFP 的转基因小鼠、定量 RT-PCR 和免疫荧光染色来确定 CTGF 的表达。携带两个 floxed CTGF 等位基因和在人泛素 C(ubc)启动子控制下的 Cre/ERT2 转基因的小鼠用于在他莫昔芬诱导下条件性删除 CTGF 基因。光疗性角膜切削术(PTK)用于产生急性角膜伤口,并通过荧光素染色评估角膜再上皮化。
CTGF 表达在多种眼部组织中,角膜内皮、晶状体囊下上皮和虹膜及视网膜血管中表达水平较高。受伤的角膜对伤口边缘上皮细胞中 CTGF 的即刻上调以及再上皮化过程中的持续 CTGF 诱导有反应。在混浊形成开始时,CTGF 蛋白在基底层上皮中更加集中。与野生型小鼠相比,CTGF 基因缺失导致角膜再上皮化率降低 40%(P < 0.01)。
CTGF 在未受伤的角膜、晶状体、虹膜和视网膜中表达,并在上皮损伤后立即表达。CTGF 的缺失会损害角膜伤口的有效再上皮化。