Lack of Delta-Sarcoglycan (Sgcd) Results in Retinal Degeneration
2019
Andric C. Perez-Ortiz | Martha J. Peralta-Ildefonso | Esmeralda Lira-Romero | Ernesto Moya-Albor | Jorge Brieva | Israel Ramirez-Sanchez | Carmen Clapp | Alexandra Luna-Angulo | Alvaro Rendon | Elva Adan-Castro | Gabriela Ramírez-Hernández | Nundehui Díaz-Lezama | Ramón M. Coral-Vázquez | Francisco J. Estrada-Mena
Age-related macular degeneration (AMD) is the leading cause of central vision loss and severe blindness among the elderly population. Recently, we reported on the association of the SGCD gene (encoding for δ-sarcoglycan) polymorphisms with AMD. However, the functional consequence of Sgcd alterations in retinal degeneration is not known. Herein, we characterized changes in the retina of the Sgcd knocked-out mouse (KO, Sgcd<sup>−/−</sup>). At baseline, we analyzed the retina structure of three-month-old wild-type (WT, Sgcd<sup>+/+</sup>) and Sgcd<sup>−/−</sup> mice by hematoxylin and eosin (H&E) staining, assessed the Sgcd−protein complex (α-, β-, γ-, and ε-sarcoglycan, and sarcospan) by immunofluorescence (IF) and Western blot (WB), and performed electroretinography. Compared to the WT, Sgcd<sup>−/−</sup> mice are five times more likely to have retinal ruptures. Additionally, all the retinal layers are significantly thinner, more so in the inner plexiform layer (IPL). In addition, the number of nuclei in the KO versus the WT is ever so slightly increased. WT mice express Sgcd-protein partners in specific retinal layers, and as expected, KO mice have decreased or no protein expression, with a significant increase in the α subunit. At three months of age, there were no significant differences in the scotopic electroretinographic responses, regarding both a- and b-waves. According to our data, Sgcd<sup>−/−</sup> has a phenotype that is compatible with retinal degeneration.
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