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In addition to the autonomic and peripheral sensory neuropathies that challenge patient survival, one of the most debilitating symptoms affecting patients' quality of life is progressive blindness resulting from the steady loss of retinal ganglion cells (RGCs). Within the FD community, there is a concerted effort to develop treatments to prevent the loss of RGCs. However, the mechanisms underlying the death of RGCs are not well understood. To study the mechanisms underlying RGC death,\n                    <jats:italic>Pax6\u2010cre;Elp1<\/jats:italic>\n                    <jats:sup>\n                      <jats:italic>loxp\/loxp<\/jats:italic>\n                    <\/jats:sup>\n                    male and female mice and postmortem retinal tissue from an FD patient were used to explore the neuronal and non\u2010neuronal cellular pathology associated with the FD optic neuropathy. Neurons, astrocytes, microglia, M\u00fcller glia, and endothelial cells were investigated using a combination of histological analyses. We identified a novel disruption of cellular homeostasis and gliosis in the FD retina. Beginning shortly after birth and progressing with age, the FD retina is marked by astrogliosis and perturbations in microglia, which coincide with vascular remodeling. These changes begin before the onset of RGC death, suggesting alterations in the retinal neurovascular unit may contribute to and exacerbate RGC death. We reveal for the first time that the FD retina pathology includes reactive gliosis, increased microglial recruitment to the ganglion cell layer (GCL), disruptions in the deep and superficial vascular plexuses, and alterations in signaling pathways. These studies implicate the neurovascular unit as a disease\u2010modifying target for therapeutic interventions in FD.\n                  <\/jats:p>","DOI":"10.1002\/glia.24612","type":"journal-article","created":{"date-parts":[[2024,9,4]],"date-time":"2024-09-04T01:09:11Z","timestamp":1725412151000},"page":"2268-2294","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Neuronal and glial cell alterations involved in the retinal degeneration of the familial dysautonomia optic neuropathy"],"prefix":"10.1002","volume":"72","author":[{"ORCID":"https:\/\/orcid.org\/0009-0009-6323-8407","authenticated-orcid":false,"given":"Anastasia","family":"Schultz","sequence":"first","affiliation":[{"name":"Department of Microbiology and Cell Biology Montana State University  Bozeman Montana 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