Functional connexin35 increased in the myopic chicken retina.

IF 2.3 4区 医学 Q4 NEUROSCIENCES
Seema Banerjee, Qing Wang, George Tang, ChungHim So, Sze Wan Shan, King Kit Li, Chi-Wai Do, Feng Pan
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引用次数: 3

Abstract

Our previous research showed that increased phosphorylation of connexin (Cx)36 indicated extended  coupling of AII amacrine cells (ACs) in the rod-dominant mouse myopic retina. This research will determine whether phosphorylation at serine 276 of Cx35-containing gap junctions increased in the myopic chicken, whose retina is cone-dominant. Refractive errors and ocular biometric dimensions of 7-days-old chickens were determined following 12 h and 7 days induction of myopia by a -10D lens. The expression pattern and size of Cx35-positive plaques were examined in the early (12 h) and compensated stages (7 days) of lens-induced myopia (LIM). At the same time, phosphorylation at serine 276 (functional assay) of Cx35 in strata 5 (S5) of the inner plexiform layer was investigated. The axial length of the 7 days LIM eyes was significantly longer than that of non-LIM controls (P < 0.05). Anti-phospho-Ser276 (Ser276-P)-labeled plaques were significantly increased in LIM retinas at both 12 h and 7 days. The density of Ser276-P of Cx35 was observed to increase after 12 h LIM. In the meanwhile, the areas of existing Cx35 plaques did not change. As there was more phosphorylation of connexin35 at Ser276 at both the early and late stages (12 h) and 7 days of LIM chicken retinal activity, the coupling with ACs could be increased in myopia development of the cone-dominated chicken retina.

Abstract Image

Abstract Image

Abstract Image

功能性连接蛋白35在近视鸡视网膜中增加。
我们之前的研究表明,连接蛋白(Cx)36磷酸化的增加表明在杆状优势小鼠近视视网膜中AII无分泌细胞(ACs)的扩展偶联。本研究将确定含cx35间隙连接的276丝氨酸磷酸化是否在视网膜锥体显性的近视鸡中增加。采用-10D晶状体诱导7日龄鸡近视12 h和7 d,测定其屈光不正和眼部生物特征尺寸。在晶状体性近视(LIM)早期(12 h)和代偿期(7 d)检测cx35阳性斑块的表达模式和大小。同时,对内丛状层第5层(S5) Cx35丝氨酸276位点的磷酸化(功能测定)进行了研究。与非LIM对照组相比,LIM组7天眼轴长显著增加(P . 539)
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来源期刊
Visual Neuroscience
Visual Neuroscience 医学-神经科学
CiteScore
2.20
自引率
5.30%
发文量
8
审稿时长
>12 weeks
期刊介绍: Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.
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