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Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degeneration.
Voigt, Andrew P; Mullin, Nathaniel K; Mulfaul, Kelly; Lozano, Lola P; Wiley, Luke A; Flamme-Wiese, Miles J; Boese, Erin A; Han, Ian C; Scheetz, Todd E; Stone, Edwin M; Tucker, Budd A; Mullins, Robert F.
Afiliación
  • Voigt AP; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Mullin NK; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
  • Mulfaul K; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Lozano LP; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
  • Wiley LA; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Flamme-Wiese MJ; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
  • Boese EA; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Han IC; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
  • Scheetz TE; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Stone EM; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
  • Tucker BA; Department of Ophthalmology and Visual Sciences, The University of Iowa Carver College of Medicine, Iowa City, IA 52242, USA.
  • Mullins RF; Institute for Vision Research, The University of Iowa, Iowa City, IA 52242, USA.
Hum Mol Genet ; 31(14): 2406-2423, 2022 07 21.
Article en En | MEDLINE | ID: mdl-35181781
The human choroid is a heterogeneous, highly vascular connective tissue that dysfunctions in age-related macular degeneration (AMD). In this study, we performed single-cell RNA sequencing on 21 human choroids, 11 of which were derived from donors with early atrophic or neovascular AMD. Using this large donor cohort, we identified new gene expression signatures and immunohistochemically characterized discrete populations of resident macrophages, monocytes/inflammatory macrophages and dendritic cells. These three immune populations demonstrated unique expression patterns for AMD genetic risk factors, with dendritic cells possessing the highest expression of the neovascular AMD-associated MMP9 gene. Additionally, we performed trajectory analysis to model transcriptomic changes across the choroidal vasculature, and we identified expression signatures for endothelial cells from choroidal arterioles and venules. Finally, we performed differential expression analysis between control, early atrophic AMD, and neovascular AMD samples, and we observed that early atrophic AMD samples had high expression of SPARCL1, a gene that has been shown to increase in response to endothelial damage. Likewise, neovascular endothelial cells harbored gene expression changes consistent with endothelial cell damage and demonstrated increased expression of the sialomucins CD34 and ENCM, which were also observed at the protein level within neovascular membranes. Overall, this study characterizes the molecular features of new populations of choroidal endothelial cells and mononuclear phagocytes in a large cohort of AMD and control human donors.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neovascularización Coroidal / Degeneración Macular Húmeda Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neovascularización Coroidal / Degeneración Macular Húmeda Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos