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A Population Study of Common Ocular Abnormalities in C57BL/6N rd8 Mice.
Moore, Bret A; Roux, Michel J; Sebbag, Lionel; Cooper, Ann; Edwards, Sydney G; Leonard, Brian C; Imai, Denise M; Griffey, Stephen; Bower, Lynette; Clary, Dave; Lloyd, K C Kent; Hérault, Yann; Thomasy, Sara M; Murphy, Christopher J; Moshiri, Ala.
Afiliación
  • Moore BA; William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.
  • Roux MJ; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France.
  • Sebbag L; Centre National de la Recherche Scientifique, UMR7104, Illkirch, France.
  • Cooper A; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France.
  • Edwards SG; Université de Strasbourg, Illkirch, France.
  • Leonard BC; William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.
  • Imai DM; William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.
  • Griffey S; William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.
  • Bower L; William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.
  • Clary D; Comparative Pathology Laboratory, School of Veterinary Medicine, UC Davis, Davis, California, United States.
  • Lloyd KCK; Comparative Pathology Laboratory, School of Veterinary Medicine, UC Davis, Davis, California, United States.
  • Hérault Y; Mouse Biology Program, University of California-Davis, Davis, California, United States.
  • Thomasy SM; Mouse Biology Program, University of California-Davis, Davis, California, United States.
  • Murphy CJ; Mouse Biology Program, University of California-Davis, Davis, California, United States.
  • Moshiri A; Department of Surgery, School of Medicine, University of California-Davis, Sacramento, California, United States.
Invest Ophthalmol Vis Sci ; 59(6): 2252-2261, 2018 05 01.
Article en En | MEDLINE | ID: mdl-29847629
Purpose: The purpose of this study was to quantify the frequency and severity of ocular abnormalities affecting wild-type C57BL/6N mice, the most common strain used worldwide for the creation of single-gene knockouts. Methods: A total of 2773 animals (5546 eyes) were examined at one colony at UC Davis and in three more colonies at the Institut Clinique de la Souris in Strasbourg, France. Mice were examined at 15 to 16 weeks postnatal age by performing anterior segment biomicroscopy, posterior segment examination by indirect ophthalmoscopy, intraocular pressure measurement, and optical coherence tomography of anterior and posterior segment structures. Results: Common ocular findings in the C57BL/6N strain included corneal deposits (3%), increased optical density of the anterior lens capsule (67%), punctate nuclear cataracts (98%), vitreous crystalline deposits (61%), hyaloid vascular remnant (6%), and retinal dysplasia attributed to the rd8 mutation (58%). Interestingly, retinal dysplasia was more common in male mice in all four breeding colonies evaluated in this study. The thickness of ocular tissues and compartments were measured by spectral-domain optical coherence tomography, including the central cornea, anterior chamber, vitreous, and retinal layers. Intraocular pressure was measured by rebound tonometry. Conclusions: Ocular abnormalities are common in anterior and posterior segments of the C57BL/6N mouse, the most common background on which single-gene knockout mice have been made. It is important that vision scientists understand the extent and variability of ocular findings associated with this particular genetic background of mice.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / Proteínas Nucleares / Anomalías del Ojo / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN / Proteínas Nucleares / Anomalías del Ojo / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos