School of Optometry and Ophthalmology, and Eye Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
State Key Laboratory and Key Laboratory of Vision Science, Ministry of Health People's Republic of China and Zhejiang Provincial Key Laboratory of Ophthalmology and Optometry, Wenzhou, Zhejiang, China.
Invest Ophthalmol Vis Sci. 2021 Jul 1;62(9):27. doi: 10.1167/iovs.62.9.27.
The purpose of this study was to determine whether retinal gap junctions (GJs) via connexin 36 (Cx36, mediating coupling of many retinal cell types) and horizontal cell (HC-HC) coupling, are involved in emmetropization.
Guinea pigs (3 weeks old) were monocularly form deprived (FD) or raised without FD (in normal visual [NV] environment) for 2 days or 4 weeks; alternatively, they wore a -4 D lens (hyperopic defocus [HD]) or 0 D lens for 2 days or 1 week. FD and NV eyes received daily subconjunctival injections of a nonspecific GJ-uncoupling agent, 18-β-Glycyrrhetinic Acid (18-β-GA). The amounts of total Cx36 and of phosphorylated Cx36 (P-Cx36; activated state that increases cell-cell coupling), in the inner and outer plexiform layers (IPLs and OPLs), were evaluated by quantitative immunofluorescence (IF), and HC-HC coupling was evaluated by cut-loading with neurobiotin.
FD per se (excluding effect of light-attenuation) increased HC-HC coupling in OPL, whereas HD did not affect it. HD for 2 days or 1 week had no significant effect on retinal content of Cx36 or P-Cx36. FD for 4 weeks decreased the total amounts of Cx36 and P-Cx36, and the P-Cx36/Cx36 ratio, in the IPL. Subconjunctival 18-β-GA induced myopia in NV eyes and increased the myopic shifts in FD eyes, while reducing the amounts of Cx36 and P-Cx36 in both the IPL and OPL.
These results suggest that cell-cell coupling via GJs containing Cx36 (particularly those in the IPL) plays a role in emmetropization and form deprivation myopia (FDM) in mammals. Although both FD and 18-β-GA induced myopia, they had opposite effects on HC-HC coupling. These findings suggest that HC-HC coupling in the OPL might not play a significant role in emmetropization and myopia development.
本研究旨在确定视网膜缝隙连接(GJ)通过连接蛋白 36(Cx36,介导多种视网膜细胞类型的偶联)和水平细胞(HC-HC)偶联是否参与正视化过程。
将豚鼠(3 周龄)单眼形觉剥夺(FD)或在正常视觉(NV)环境中饲养(无 FD)2 天或 4 周;或者,它们佩戴-4 D 透镜(远视离焦[HD])或 0 D 透镜 2 天或 1 周。FD 和 NV 眼每日接受结膜下注射非特异性 GJ 解偶联剂 18-β-甘草次酸(18-β-GA)。通过定量免疫荧光(IF)评估内丛状层(IPL)和外丛状层(OPL)中总 Cx36 和磷酸化 Cx36(P-Cx36;增加细胞间偶联的激活状态)的含量,并通过神经生物素切割加载评估 HC-HC 偶联。
FD 本身(不包括光衰减的影响)增加了 OPL 中的 HC-HC 偶联,而 HD 则没有影响。HD 持续 2 天或 1 周对视网膜 Cx36 或 P-Cx36 的含量没有显著影响。FD 持续 4 周降低了 IPL 中总 Cx36 和 P-Cx36 的含量以及 P-Cx36/Cx36 比值。结膜下注射 18-β-GA 诱导 NV 眼近视,并增加 FD 眼的近视漂移,同时降低 IPL 和 OPL 中 Cx36 和 P-Cx36 的含量。
这些结果表明,包含 Cx36 的 GJ 介导的细胞间偶联(特别是 IPL 中的偶联)在哺乳动物的正视化和形觉剥夺性近视(FDM)中发挥作用。尽管 FD 和 18-β-GA 都诱导了近视,但它们对 HC-HC 偶联有相反的影响。这些发现表明,OPL 中的 HC-HC 偶联可能在正视化和近视发展中不起重要作用。