Lu Xiaowen, Elizondo Rodolfo A, Nielsen Rikke, Christensen Erik I, Yang Jun, Hammock Bruce D, Watsky Mitchell A
Department of Cell Biology and Anatomy Georgia Regents University, Augusta, Georgia, United States.
Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Invest Ophthalmol Vis Sci. 2015 Sep;56(10):5880-7. doi: 10.1167/iovs.15-17177.
To determine the source(s) of vitamin D in tear fluid and examine the expression of the endocytic proteins and putative vitamin D transporters megalin and cubilin in lacrimal and Harderian glands.
Wild-type, heterozygous, and vitamin D receptor (VDR) knockout C57BL/6 mice were used, with a subset of knockout mice fed a replenishment diet for some studies. Mouse lacrimal and Harderian glands from each group were used to measure megalin and cubilin by RT-PCR, Western blot, and immunohistochemistry. New Zealand white rabbits were used to collect lacrimal and accessory gland fluid for vitamin D mass spectroscopy measurements.
Ten-week-old knockout mice were significantly (P < 0.05) smaller than wild-type mice. Real-time PCR and Western blot showed decreased expression of megalin and cubilin in select VDR knockout mouse groups. Immunohistochemistry showed apical duct cell megalin staining and weaker megalin staining in VDR knockout mice compared with controls. Vitamin D2 was more prevalent in rabbit lacrimal and accessory gland fluid than vitamin D3, and greater amounts of Vitamin D2 were found in in tear fluid obtained directly from lacrimal and accessory glands as compared with plasma concentrations.
This is the first study to demonstrate the presence of megalin and cubilin in lacrimal and accessory glands responsible for producing tear fluid. The results strengthen the hypothesis that megalin and cubilin are likely involved in the secretory pathway of vitamin D into tear fluid by the duct cells.
确定泪液中维生素D的来源,并检测泪腺和哈德氏腺中内吞蛋白及假定的维生素D转运蛋白巨膜蛋白和立方蛋白的表达。
使用野生型、杂合型和维生素D受体(VDR)基因敲除的C57BL/6小鼠,部分基因敲除小鼠在一些研究中喂食补充饮食。每组小鼠的泪腺和哈德氏腺用于通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫组织化学检测巨膜蛋白和立方蛋白。使用新西兰白兔收集泪液和副腺液进行维生素D质谱测量。
10周龄的基因敲除小鼠明显(P < 0.05)比野生型小鼠小。实时PCR和蛋白质免疫印迹法显示,在选定的VDR基因敲除小鼠组中,巨膜蛋白和立方蛋白的表达降低。免疫组织化学显示,与对照组相比,VDR基因敲除小鼠的顶端导管细胞有巨膜蛋白染色,且巨膜蛋白染色较弱。维生素D2在兔泪液和副腺液中比维生素D3更普遍,与血浆浓度相比,直接从泪腺和副腺获得的泪液中发现了更多的维生素D2。
这是第一项证明在产生泪液的泪腺和副腺中存在巨膜蛋白和立方蛋白的研究。结果强化了以下假设,即巨膜蛋白和立方蛋白可能参与导管细胞将维生素D分泌到泪液中的途径。