| Literature DB >> 34297923 |
Xinzheng Guo1, Jing Zhou1, Christopher Starr1, Ethan J Mohns2, Yidong Li2, Earnest P Chen3, Yonejung Yoon4, Christopher P Kellner4, Kohichi Tanaka5, Hongbing Wang6, Wei Liu7, Louis R Pasquale1, Jonathan B Demb8, Michael C Crair9, Bo Chen10.
Abstract
Retinal ganglion cells (RGCs) are the sole output neurons that transmit visual information from the retina to the brain. Diverse insults and pathological states cause degeneration of RGC somas and axons leading to irreversible vision loss. A fundamental question is whether manipulation of a key regulator of RGC survival can protect RGCs from diverse insults and pathological states, and ultimately preserve vision. Here, we report that CaMKII-CREB signaling is compromised after excitotoxic injury to RGC somas or optic nerve injury to RGC axons, and reactivation of this pathway robustly protects RGCs from both injuries. CaMKII activity also promotes RGC survival in the normal retina. Further, reactivation of CaMKII protects RGCs in two glaucoma models where RGCs degenerate from elevated intraocular pressure or genetic deficiency. Last, CaMKII reactivation protects long-distance RGC axon projections in vivo and preserves visual function, from the retina to the visual cortex, and visually guided behavior.Entities:
Keywords: CREB; CaMKII; RGC; RGC protection; excitotoxicity; glaucoma; optic nerve crush; vision preservation; visual function; visual pathway
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Year: 2021 PMID: 34297923 PMCID: PMC8530265 DOI: 10.1016/j.cell.2021.06.031
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 66.850