Mouse model of ocular hypertension with retinal ganglion cell degeneration

Autor: Eiichi Hasegawa, Ryo Mukai, Meredith S Gregory-Ksander, Kip M. Connor, Yoko Okunuki, Anitha Krishnan, Garrett Klokman, Dong Ho Park, Joan W. Miller, Deeba Husain, Clifford Kim
Rok vydání: 2019
Předmět:
Male
Retinal Ganglion Cells
0301 basic medicine
Intraocular pressure
Eye Diseases
genetic structures
Polymers
Ocular hypertension
Glaucoma
Blood Pressure
Degeneration (medical)
Vascular Medicine
Cornea
Mice
0302 clinical medicine
Animal Cells
Medicine and Health Sciences
Materials
Neurons
Multidisciplinary
Retinal Degeneration
Immunohistochemistry
Chemistry
medicine.anatomical_structure
Macromolecules
Retinal ganglion cell
Physical Sciences
Hypertension
Medicine
Cellular Types
Anatomy
Tomography
Optical Coherence

Research Article
medicine.medical_specialty
Programmed cell death
Ganglion Cells
Science
Ocular Anatomy
Materials Science
Retina
Microbeads
03 medical and health sciences
Ocular System
Ophthalmology
medicine
Animals
Intraocular Pressure
business.industry
Biology and Life Sciences
Afferent Neurons
Cell Biology
Polymer Chemistry
medicine.disease
eye diseases
Mice
Inbred C57BL

Disease Models
Animal

030104 developmental biology
Cellular Neuroscience
030221 ophthalmology & optometry
Eyes
Ocular Hypertension
sense organs
business
Head
Neuroscience
Zdroj: PLoS ONE
PLoS ONE, Vol 14, Iss 1, p e0208713 (2019)
ISSN: 1932-6203
Popis: ObjectivesOcular hypertension is a primary risk factor for glaucoma and results in retinal ganglion cell (RGC) degeneration. Current animal models of glaucoma lack severe RGC cell death as seen in glaucoma, making assessment of physiological mediators of cell death difficult. We developed a modified mouse model of ocular hypertension whereby long-lasting elevation of intraocular pressure (IOP) is achieved, resulting in significant reproducible damage to RGCs.ResultsIn this model, microbeads are mixed with hyaluronic acid and injected into the anterior chamber of C57BL/6J mice. The hyaluronic acid allows for a gradual release of microbeads, resulting in sustained blockage of Schlemm's canal. IOP elevation was bimodal during the course of the model's progression. The first peak occurred 1 hours after beads injection, with an IOP value of 44.69 ± 6.00 mmHg, and the second peak occurred 6-12 days post-induction, with an IOP value of 34.91 ± 5.21 mmHg. RGC damage was most severe in the peripheral retina, with a loss of 64.1% compared to that of untreated eyes, while the midperiphery exhibited a 32.4% loss, 4 weeks following disease induction.ConclusionsThese results suggest that sustained IOP elevation causes more RGC damage in the periphery than in the midperiphery of the retina. This model yields significant and reproducible RGC degeneration.
Databáze: OpenAIRE