Imaging retinal ganglion cells: Enabling experimental technology for clinical application

Corey A. Smith, Balwantray C. Chauhan

Producción científica: Contribución a una revistaArtículo de revisiónrevisión exhaustiva

28 Citas (Scopus)

Resumen

Recent advances in clinical ophthalmic imaging have enhanced patient care. However, the ability to differentiate retinal neurons, such as retinal ganglion cells (RGCs), would advance many areas within ophthalmology, including the screening and monitoring of glaucoma and other optic neuropathies. Imaging at the single cell level would take diagnostics to the next level. Experimental methods have provided techniques and insight into imaging RGCs, however no method has yet to be translated to clinical application. This review provides an overview of the importance of non-invasive imaging of RGCs and the clinically relevant capabilities. In addition, we report on experimental data from wild-type mice that received an invivo intravitreal injection of a neuronal tracer that labelled RGCs, which in turn were monitored for up to 100 days post-injection with confocal scanning laser ophthalmoscopy. We were able to demonstrate efficient and consistent RGC labelling with this delivery method and discuss the issue of cell specificity. This type of experimental work is important in progressing towards clinically applicable methods for monitoring loss of RGCs in glaucoma and other optic neuropathies. We discuss the challenges to translating these findings to clinical application and how this method of tracking RGCs invivo could provide valuable structural and functional information to clinicians.

Idioma originalEnglish
Páginas (desde-hasta)1-14
Número de páginas14
PublicaciónProgress in Retinal and Eye Research
Volumen44
DOI
EstadoPublished - ene. 1 2015

Nota bibliográfica

Funding Information:
The authors are very grateful to Michele Archibald, Kelly Stevens, Xu Wang, Andrea Nuschke and Julie Levesque for their input and technical support. We thank Dr. Nicholas Brecha for the RBPMS antibody. We also thank the three anonymous reviewers of this manuscript for their constructive comments. This research was supported by the Atlantic Canada Opportunities Agency, Atlantic Innovation Fund 197809 . The funder had no role in study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the article for publication.

Publisher Copyright:
© 2014 Elsevier Ltd.

ASJC Scopus Subject Areas

  • Ophthalmology
  • Sensory Systems

PubMed: MeSH publication types

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

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