Functional connexin35 increased in the myopic chicken retina.


Journal

Visual neuroscience
ISSN: 1469-8714
Titre abrégé: Vis Neurosci
Pays: England
ID NLM: 8809466

Informations de publication

Date de publication:
14 05 2021
Historique:
entrez: 14 5 2021
pubmed: 15 5 2021
medline: 29 10 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 33988110
doi: 10.1017/S0952523821000079
pii: S0952523821000079
pmc: PMC8167454
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

E008

Commentaires et corrections

Type : ErratumIn

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Auteurs

Seema Banerjee (S)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

Qing Wang (Q)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

George Tang (G)

School of Clinical Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, United Kingdom.

ChungHim So (C)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

Sze Wan Shan (SW)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

King Kit Li (KK)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.

Chi-Wai Do (CW)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Centre for Eye and Vision Research (CEVR), 17W Hong Kong Science Park, Hong Kong.

Feng Pan (F)

School of Optometry, The Hong Kong Polytechnic University, Kowloon, Hong Kong.
Centre for Eye and Vision Research (CEVR), 17W Hong Kong Science Park, Hong Kong.

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Classifications MeSH