Dysfunctional cGMP Signaling Leads to Age-Related Retinal Vascular Alterations and Astrocyte Remodeling in Mice |
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Authors: | Joseph M Holden Sara Al Hussein Al Awamlh Louis-Philippe Croteau Andrew M Boal Tonia S Rex Michael L Risner David J Calkins Lauren K Wareham |
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Affiliation: | Vanderbilt Eye Institute, Vanderbilt University Medical Center, Nashville, TN 37232, USA; (J.M.H.); (S.A.H.A.A.); (L.-P.C.); (A.M.B.); (T.S.R.); (M.L.R.); (D.J.C.) |
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Abstract: | The nitric oxide–guanylyl cyclase-1–cyclic guanylate monophosphate (NO–GC-1–cGMP) pathway is integral to the control of vascular tone and morphology. Mice lacking the alpha catalytic domain of guanylate cyclase (GC1−/−) develop retinal ganglion cell (RGC) degeneration with age, with only modest fluctuations in intraocular pressure (IOP). Increasing the bioavailability of cGMP in GC1−/− mice prevents neurodegeneration independently of IOP, suggesting alternative mechanisms of retinal neurodegeneration. In continuation to these studies, we explored the hypothesis that dysfunctional cGMP signaling leads to changes in the neurovascular unit that may contribute to RGC degeneration. We assessed retinal vasculature and astrocyte morphology in young and aged GC1−/− and wild type mice. GC1−/− mice exhibit increased peripheral retinal vessel dilation and shorter retinal vessel branching with increasing age compared to Wt mice. Astrocyte cell morphology is aberrant, and glial fibrillary acidic protein (GFAP) density is increased in young and aged GC1−/− mice, with areas of dense astrocyte matting around blood vessels. Our results suggest that proper cGMP signaling is essential to retinal vessel morphology with increasing age. Vascular changed are preceded by alterations in astrocyte morphology which may together contribute to retinal neurodegeneration and loss of visual acuity observed in GC1−/− mice. |
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Keywords: | retinal vasculature neurovascular unit blood retinal barrier astrocyte connexin gap junctions neurodegeneration retinal ganglion cell |
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