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Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors.
Lhussiez, Vincent; Dubus, Elisabeth; Cesar, Quénol; Acar, Niyazi; Nandrot, Emeline F; Simonutti, Manuel; Audo, Isabelle; Lizé, Eléonore; Nguyen, Sylvie; Geissler, Audrey; Bouchot, André; Ansar, Muhammad; Picaud, Serge; Thauvin-Robinet, Christel; Olivier-Faivre, Laurence; Duplomb, Laurence; Da Costa, Romain.
Afiliación
  • Lhussiez V; INSERM UMR1231, Equipe GAD, Université de Bourgogne Franche Comté, Dijon, France.
  • Dubus E; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Cesar Q; Centre des Sciences du Goût et de l'Alimentation, AgroSup Dijon, CNRS, INRAE, Université Bourgogne Franche-Comté, Dijon, France.
  • Acar N; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Nandrot EF; Centre des Sciences du Goût et de l'Alimentation, AgroSup Dijon, CNRS, INRAE, Université Bourgogne Franche-Comté, Dijon, France.
  • Simonutti M; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Audo I; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Lizé E; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Nguyen S; INSERM UMR1231, Equipe GAD, Université de Bourgogne Franche Comté, Dijon, France.
  • Geissler A; INSERM UMR1231, Equipe GAD, Université de Bourgogne Franche Comté, Dijon, France.
  • Bouchot A; Plateforme d'Imagerie Cellulaire DImaCell (site CellImaP), INSERM LNC UMR1231, Dijon, France.
  • Ansar M; Plateforme d'Imagerie Cellulaire DImaCell (site CellImaP), INSERM LNC UMR1231, Dijon, France.
  • Picaud S; Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
  • Thauvin-Robinet C; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
  • Olivier-Faivre L; Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
  • Duplomb L; INSERM UMR1231, Equipe GAD, Université de Bourgogne Franche Comté, Dijon, France.
  • Da Costa R; FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
Invest Ophthalmol Vis Sci ; 61(11): 18, 2020 09 01.
Article en En | MEDLINE | ID: mdl-32915983
Purpose: Cohen syndrome (CS) is a rare genetic disorder caused by variants of the VPS13B gene. CS patients are affected with a severe form of retinal dystrophy, and in several cases cataracts also develop. The purpose of this study was to investigate the mechanisms and risk factors for cataract in CS, as well as to report on cataract surgeries in CS patients. Methods: To understand how VPS13B is associated with visual impairments in CS, we generated the Vps13b∆Ex3/∆Ex3 mouse model. Mice from 1 to 3 months of age were followed by ophthalmoscopy and slit-lamp examinations. Phenotypes were investigated by histology, immunohistochemistry, and western blot. Literature analysis was performed to determine specific characteristic features of cataract in CS and to identify potential genotype-phenotype correlations. Results: Cataracts rapidly developed in 2-month-old knockout mice and were present in almost all lenses at 3 months. Eye fundi appeared normal until cataract development. Lens immunostaining revealed that cataract formation was associated with the appearance of large vacuoles in the cortical area, epithelial-mesenchymal transition, and fibrosis. In later stages, cataracts became hypermature, leading to profound retinal remodeling due to inflammatory events. Literature analysis showed that CS-related cataracts display specific features compared to other forms of retinitis pigmentosa-related cataracts, and their onset is modified by additional genetic factors. Corroboratively, we were able to isolate a subline of the Vps13b∆Ex3/∆Ex3 model with delayed cataract onset. Conclusions: VPS13B participates in lens homeostasis, and the CS-related cataract development dynamic is linked to additional genetic factors.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Degeneración Retiniana / Catarata / ARN / Regulación de la Expresión Génica / Proteínas de Transporte Vesicular / Dedos / Homeostasis / Cristalino / Discapacidad Intelectual / Microcefalia Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2020 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Degeneración Retiniana / Catarata / ARN / Regulación de la Expresión Génica / Proteínas de Transporte Vesicular / Dedos / Homeostasis / Cristalino / Discapacidad Intelectual / Microcefalia Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2020 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos