Toyono Tetsuya, Usui Tomohiko, Yokoo Seiichi, Taketani Yukako, Nakagawa Suguru, Kuroda Masahiko, Yamagami Satoru, Amano Shiro
Department of Ophthalmology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Department of Pathology, Tokyo Medical University, Tokyo, Japan.
PLoS One. 2015 Jan 26;10(1):e0116838. doi: 10.1371/journal.pone.0116838. eCollection 2015.
We sought to identify the anti-angiogenic molecule expressed in corneal keratocytes that is responsible for maintaining the avascularity of the cornea.
Human umbilical vein endothelial cells (HUVECs) were cultured with either human dermal fibroblasts or with human corneal keratocytes under serum-free conditions. The areas that exhibited blood vessel formation were estimated by immunostaining the cultures with an antitibody against CD31, a blood vessel marker. We also performed microarray gene-expression analysis and selected one molecule, angiopoietin-like 7 (ANGPTL7) for further functional studies conducted with the keratocytes and in vivo in mice.
Areas showing blood vessel formation in normal serum-free medium were conditions were markedly smaller when HUVECs were co-cultured with corneal keratocytes than when they were co-cultured with the dermal fibroblasts under the same conditions. Microarray analysis revealed that ANGPTL7 expression was higher in keratocytes than in dermal fibroblasts. In vitro, inhibiting ANGPTL7 expression by using a specific siRNA led to greater tube formation than did the transfection of cells with a control siRNA, and this increase in tube formation was abolished when recombinant ANGPTL7 protein was added to the cultures. In vivo, intrastromal injections of an ANGPTL7 PshRNA into the avascular corneal stroma of mice resulted in the growth of blood vessels.
ANGPTL7, which is abundantly expressed in keratocytes, plays a major role in maintaining corneal avascularity and transparency.
我们试图鉴定在角膜基质细胞中表达的抗血管生成分子,该分子负责维持角膜的无血管状态。
在无血清条件下,将人脐静脉内皮细胞(HUVECs)与人皮肤成纤维细胞或人角膜基质细胞共同培养。通过用抗血管标志物CD31的抗体对培养物进行免疫染色来估计显示血管形成的区域。我们还进行了微阵列基因表达分析,并选择了一种分子,即血管生成素样7(ANGPTL7),用于与角膜基质细胞一起进行进一步的功能研究以及在小鼠体内进行研究。
在正常无血清培养基中显示血管形成的区域,当HUVECs与角膜基质细胞共培养时,明显小于在相同条件下与皮肤成纤维细胞共培养时。微阵列分析显示,ANGPTL7在角膜基质细胞中的表达高于皮肤成纤维细胞。在体外,使用特异性siRNA抑制ANGPTL7表达导致形成的管状物比用对照siRNA转染细胞时更多,并且当将重组ANGPTL7蛋白添加到培养物中时,这种管状物形成的增加被消除。在体内,将ANGPTL7的短发夹RNA(PshRNA)基质内注射到小鼠的无血管角膜基质中导致血管生长。
在角膜基质细胞中大量表达的ANGPTL7在维持角膜无血管状态和透明度方面起主要作用。