Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin Eye Institute, Tianjin Eye Hospital, Tianjin, China.
Medical College of Optometry and Ophthalmology, Shandong University of Traditional Chinese Medicine, Jinan, China.
Invest Ophthalmol Vis Sci. 2024 Sep 3;65(11):8. doi: 10.1167/iovs.65.11.8.
This study investigates alterations in intrinsically photosensitive retinal ganglion cells (ipRGCs) and dopaminergic amacrine cells (DACs) in lid suture myopia (LSM) rats.
LSM was induced in rats by suturing the right eyes for 4 weeks. Double immunofluorescence staining of ipRGCs and DACs in whole-mount retinas was performed to analyze changes in the density and morphology of control, LSM, and fellow eyes. Real-time quantitative PCR and Western blotting were used to detect related genes and protein expression levels.
Significant myopia was induced in the lid-sutured eye, but the fellow eye was not different to control. Decreased ipRGC density with paradoxically increased overall melanopsin expression and enlarged dendritic beads was observed in both the LSM and fellow eyes of the LSM rat retinas. In contrast, DAC changes occurred only in the LSM eyes, with reduced DAC density and tyrosine hydroxylase (TH) expression, sparser dendritic processes, and fewer varicosities. Interestingly, contacts between ipRGCs and DACs in the inner plexiform layer (IPL) and the expression of pituitary adenylate cyclase-activating polypeptide (PACAP) and vesicular monoamine transporter protein 2 (VMAT2) mRNA were decreased in the LSM eyes.
The ipRGCs and DACs in LSM rat retinas undergo multiple alterations in density, morphology, and related molecule expressions. However, the ipRGC changes alone appear not to be required for the development of myopia, given that myopia is only induced in the lid-sutured eye, and they are unlikely alone to drive the DAC changes. Reduced contacts between ipRGCs and DACs in the LSM eyes may be the structural foundation for the impaired signaling between them. PACAP and VMAT2, strongly associated with ipRGCs and DACs, may play important roles in LSM through complex mechanisms.
本研究旨在探讨睑板缝合性近视(LSM)大鼠中内在光敏感视网膜神经节细胞(ipRGCs)和多巴胺能无长突细胞(DACs)的变化。
通过缝合右眼 4 周诱导 LSM 大鼠。对全视网膜铺片进行 ipRGCs 和 DACs 的双重免疫荧光染色,以分析对照眼、LSM 眼和对侧眼的密度和形态变化。实时定量 PCR 和 Western blot 用于检测相关基因和蛋白表达水平。
在缝合眼诱导出明显的近视,但对侧眼与对照眼无差异。在 LSM 大鼠视网膜中,LSM 眼和对侧眼的 ipRGC 密度降低,同时整体黑视素表达增加,树突珠增大。相比之下,只有在 LSM 眼中观察到 DAC 变化,表现为 DAC 密度和酪氨酸羟化酶(TH)表达降低,树突过程稀疏,轴突末梢减少。有趣的是,在 LSM 眼中,内丛状层(IPL)中 ipRGC 和 DAC 之间的接触减少,垂体腺苷酸环化酶激活肽(PACAP)和囊泡单胺转运蛋白 2(VMAT2)mRNA 的表达降低。
LSM 大鼠视网膜中的 ipRGCs 和 DACs 在密度、形态和相关分子表达方面发生了多种改变。然而,由于近视仅发生在缝合眼,ipRGC 的改变似乎不是近视发展所必需的,而且它们不太可能单独引起 DAC 的改变。LSM 眼中 ipRGC 和 DAC 之间的接触减少可能是它们之间信号受损的结构基础。与 ipRGCs 和 DACs 强烈相关的 PACAP 和 VMAT2 可能通过复杂机制在 LSM 中发挥重要作用。