Wang Ya-Ni, Liu Xian-Ning, Wang Xiao-Dong, Yin Yong, Chen Yan, Xiao Xiang-Hua, Xu Kun, Zhu Xiu-Ping
Xi'an No.1 Hospital; Shaanxi Institute of Ophthalmology, Shaanxi Key Laboratory of Ophthalmology; Clinical Research Center for Ophthalmology Diseases of Shaanxi Province; First Affiliated Hospital of Northwestern University, Xi'an 710002, Shaanxi Province, China.
Int J Ophthalmol. 2019 Feb 18;12(2):201-206. doi: 10.18240/ijo.2019.02.03. eCollection 2019.
To investigate the expression of visual system homeobox 1 (VSX1) and myofibroblast marker alpha smooth muscle actin (α-SMA) in keratoconus (KC).
Thirty corneal tissue were collected from KC patients after corneal transplantation and 15 normal donor corneas were obtained. All corneal tissues divided into 4 parts for different detections. Scanning electron microscopy was used to observe the ultrastructure of the specimens. VSX1 and α-SMA localization in cornea tissues was detected using immunofluorescence histochemistry. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and Western blot were performed to analyze the expression level of VSX1 and α-SMA.
Compared to normal cornea tissue, the collagen fibers in KC stroma were distortional and attenuated and keratocytes were abnormally changed. VSX1 and α-SMA located in the corneal stroma. The mRNA and protein expression level of VSX1 in KC were about 3 times as high as that of normal tissue (<0.001). α-SMA was hardly expressed in the normal corneas, however, its expression in the KC was about 1.5 times higher than that of the normal corneas (<0.0001).
Compared with normal corneal the expression of VSX1 and α-SMA in KC both increased. VSX1 is related to the activation of keratocytes and involved in the pathogenesis of keratoconus.
研究视觉系统同源盒1(VSX1)和成肌纤维细胞标志物α平滑肌肌动蛋白(α-SMA)在圆锥角膜(KC)中的表达。
收集30例圆锥角膜患者角膜移植后的角膜组织,并获取15例正常供体角膜。所有角膜组织均分成4份用于不同检测。采用扫描电子显微镜观察标本的超微结构。利用免疫荧光组织化学检测角膜组织中VSX1和α-SMA的定位。进行逆转录-定量聚合酶链反应(RT-qPCR)和蛋白质印迹法分析VSX1和α-SMA的表达水平。
与正常角膜组织相比,圆锥角膜基质中的胶原纤维扭曲且变细,角膜细胞发生异常改变。VSX1和α-SMA定位于角膜基质。圆锥角膜中VSX1的mRNA和蛋白表达水平约为正常组织的3倍(<0.001)。α-SMA在正常角膜中几乎不表达,然而,其在圆锥角膜中的表达比正常角膜高约1.5倍(<0.0001)。
与正常角膜相比,圆锥角膜中VSX1和α-SMA的表达均增加。VSX1与角膜细胞的激活有关,并参与圆锥角膜的发病机制。