Ma Nan, Siegfried Carla, Kubota Miyuki, Huang Jie, Liu Ying, Liu Margaret, Dana Belinda, Huang Andrew, Beebe David, Yan Hong, Shui Ying-Bo
Department of Ophthalmology and Visual Sciences Washington University School of Medicine, St. Louis, Missouri, United States 2Department of Ophthalmology, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Department of Ophthalmology and Visual Sciences Washington University School of Medicine, St. Louis, Missouri, United States.
Invest Ophthalmol Vis Sci. 2016 Jun 1;57(7):3440-50. doi: 10.1167/iovs.16-19162.
Ascorbic acid (AsA) is an important antioxidant in the eye. Ascorbic acid is usually transported by sodium-dependent AsA transporters (SVCTs), and dehydroascorbic acid (DHA) by glucose transporters (GLUTs). This study investigates these AsA-related transporters in human compared with mouse eyes.
Five pairs of human donor eyes and 15 pairs of mouse eyes were collected. Immunofluorescence and in situ hybridization were performed to detect SVCTs and GLUTs expression in the ciliary epithelium, retina, and lens epithelial cells (LECs). These tissues were isolated with laser microdissection followed by extraction of total RNA. Quantitative PCR (qPCR) was performed to examine the mRNA level of SVCTs and GLUTs in human and mouse ocular tissues.
Immunofluorescence and in situ hybridization showed SVCT2 and GLUT1 expression in human ciliary epithelium with varied distributions. Sodium-dependent AsA transporter 2 is expressed only in the pigmented epithelium (PE), and GLUT1 is predominately expressed in the nonpigmented epithelium (NPE). However, SVCT2 was not identified in mouse ciliary epithelium, whereas GLUT1 expressed in both PE and NPE. Laser microdissection and qPCR revealed high levels of SVCT2 mRNA in human RPE cells and murine neural retina. Sodium-dependent AsA transporter 1 mRNA could be detected only in human and murine LECs. Glucose transporter 3 and GLUT4 mRNA could not be detected in either the human or mouse ciliary processes or in the lens epithelium.
These fundamental findings indicate AsA transporter expression in eyes of humans is significantly different compared with mice. This may explain why human aqueous and vitreous humors contain higher AsA levels compared with other animals.
抗坏血酸(AsA)是眼睛中的一种重要抗氧化剂。抗坏血酸通常由钠依赖性抗坏血酸转运体(SVCTs)转运,而脱氢抗坏血酸(DHA)则由葡萄糖转运体(GLUTs)转运。本研究比较了人类和小鼠眼睛中这些与抗坏血酸相关的转运体。
收集了5对人类供体眼睛和15对小鼠眼睛。进行免疫荧光和原位杂交以检测睫状体上皮、视网膜和晶状体上皮细胞(LECs)中SVCTs和GLUTs的表达。用激光显微切割分离这些组织,随后提取总RNA。进行定量PCR(qPCR)以检测人类和小鼠眼组织中SVCTs和GLUTs的mRNA水平。
免疫荧光和原位杂交显示,人类睫状体上皮中SVCT2和GLUT1表达,分布各异。钠依赖性抗坏血酸转运体2仅在色素上皮(PE)中表达,而GLUT1主要在非色素上皮(NPE)中表达。然而,在小鼠睫状体上皮中未鉴定出SVCT2,而GLUT1在PE和NPE中均有表达。激光显微切割和qPCR显示,人类视网膜色素上皮(RPE)细胞和小鼠神经视网膜中SVCT2 mRNA水平较高。钠依赖性抗坏血酸转运体1 mRNA仅在人类和小鼠的LECs中可检测到。在人类或小鼠的睫状体或晶状体上皮中均未检测到葡萄糖转运体3和GLUT4 mRNA。
这些基础研究结果表明,人类眼睛中抗坏血酸转运体的表达与小鼠相比有显著差异。这可能解释了为什么与其他动物相比,人类房水和玻璃体液中抗坏血酸水平更高。