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Differential Distribution of RBPMS in Pig, Rat, and Human Retina after Damage
Xandra Pereiro1, Noelia Ruzafa1, J Haritz Urcola1,2
1Department of Cell Biology and Histology, Experimental Ophthalmo-Biology Group (GOBE), University of the Basque Country UPV/EHU, 48940 Leioa, Vizcaya, Spain.
International Journal of Molecular Sciences
|December 10, 2020
Summary
RNA binding protein with multiple splicing (RBPMS) shifts location in retinal ganglion cells (RGCs) during hypoxia, moving to dendrites and axons. This suggests RBPMS plays a role in RGC damage response.
Area of Science:
- Neuroscience
- Cell Biology
- Ophthalmology
Background:
- RNA binding protein with multiple splicing (RBPMS) is found in retinal ganglion cells (RGCs) across many species.
- The function of RBPMS in RGCs and its response to injury remain largely unknown.
Purpose of the Study:
- To investigate the expression and localization of RBPMS in mammalian retinas under various conditions.
- To explore the potential role of RBPMS in retinal damage and degeneration.
Main Methods:
- Immunohistochemical analysis of RBPMS expression in retinas from humans, pigs, and rats.
- Examination of retinas at different developmental stages (neonatal, adult) and injury levels (control, hypoxia, organotypic culture).
Main Results:
- RBPMS is localized in RGC somas under normal conditions.
- Hypoxia induces a shift in RBPMS localization to RGC dendrites in the inner plexiform layer.
- RBPMS is also found in degenerating RGC axons in the nerve fiber layer of retinal explants.
Conclusions:
- RBPMS exhibits dynamic localization in RGCs in response to physiological stress like hypoxia.
- The findings suggest RBPMS may be involved in axonal and dendritic degeneration processes in the mammalian retina.
- Further research into RBPMS is warranted to understand its role in retinal damage and potential therapeutic strategies.

