Wang Eddie, Geng Andrew, Maniar Ankur M, Mui Byron W H, Gong Xiaohua
Invest Ophthalmol Vis Sci. 2016 Jun 1;57(7):3039-46. doi: 10.1167/iovs.16-19521.
The roles of gap junction protein connexin 50 (Cx50) encoded by Gja8, during lens development are not fully understood. Connexin 50 knockout (KO) lenses have decreased proliferation of epithelial cells and altered fiber cell denucleation. We further investigated the mechanism for cellular defects in Cx50 KO (Gja8-/-) lenses.
Fiber cell morphology and subcellular distribution of various lens membrane/cytoskeleton proteins from wild-type and Cx50 KO mice were visualized by immunofluorescent staining and confocal microscopy.
We observed multiple morphological defects in the cortical fibers of Cx50 KO lenses, including abnormal fiber cell packing geometry, decreased F-actin enrichment at tricellular vertices, and disrupted ball-and-socket (BS) structures on the long sides of hexagonal fibers. Moreover, only small gap junction plaques consisting of Cx46 (α3 connexin) were detected in cortical fibers and the distributions of the BS-associated beta-dystroglycan and ZO-1 proteins were altered.
Connexin 50 gap junctions are important for BS structure maturation and cortical fiber cell organization. Connexin 50-based gap junction plaques likely form structural domains with an array of membrane/cytoskeletal proteins to stabilize BS. Loss of Cx50-mediated coupling, BS disruption, and altered F-actin in Cx50 KO fibers, thereby contribute to the small lens and mild cataract phenotypes.
由Gja8编码的间隙连接蛋白连接蛋白50(Cx50)在晶状体发育过程中的作用尚未完全明确。连接蛋白50基因敲除(KO)的晶状体上皮细胞增殖减少,纤维细胞核脱失改变。我们进一步研究了Cx50基因敲除(Gja8-/-)晶状体细胞缺陷的机制。
通过免疫荧光染色和共聚焦显微镜观察野生型和Cx50基因敲除小鼠各种晶状体膜/细胞骨架蛋白的纤维细胞形态和亚细胞分布。
我们在Cx50基因敲除晶状体的皮质纤维中观察到多种形态学缺陷,包括纤维细胞堆积几何形状异常、三细胞顶点处F-肌动蛋白富集减少以及六边形纤维长边的球窝(BS)结构破坏。此外,在皮质纤维中仅检测到由Cx46(α3连接蛋白)组成的小间隙连接斑,并且与BS相关的β- dystroglycan和ZO-1蛋白的分布发生了改变。
连接蛋白50间隙连接对于BS结构成熟和皮质纤维细胞组织很重要。基于连接蛋白50的间隙连接斑可能与一系列膜/细胞骨架蛋白形成结构域以稳定BS。Cx50基因敲除纤维中Cx50介导的偶联丧失、BS破坏和F-肌动蛋白改变,从而导致晶状体小和轻度白内障表型。