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Imaging macular carotenoids and their related proteins in the human retina with confocal resonance Raman and fluorescence microscopy.
Li, Binxing; Chang, Fu-Yen; Wan, Zihe; Giauque, Nathan A; Addo, Emmanuel K; Bernstein, Paul S.
Afiliação
  • Li B; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA. Electronic address: binxing.li@hsc.utah.edu.
  • Chang FY; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA.
  • Wan Z; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA.
  • Giauque NA; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA.
  • Addo EK; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA.
  • Bernstein PS; Department of Ophthalmology and Visual Sciences, School of Medicine, University of Utah, Salt Lake City, UT, 84132, USA. Electronic address: paul.bernstein@hsc.utah.edu.
Exp Eye Res ; 247: 110043, 2024 Oct.
Article em En | MEDLINE | ID: mdl-39151780
ABSTRACT
Lutein and zeaxanthin are highly concentrated at the central region of the human retina, forming a distinct yellow spot known as the macula lutea. The delivery and retention of the macular pigment carotenoids in the macula lutea involves many proteins, but their exact roles remain incompletely understood. In our study, we examined the distribution of the twelve known macular carotenoid-related proteins within the human macula and the underlying retinal pigment epithelium (RPE) using both fluorescence and Raman modes on our confocal resonance Raman microscope. Additionally, we assessed protein and gene expression through Western blot analysis and a single-cell RNA sequencing database. Our findings revealed that GSTP1, BCO2, and Aster-B exhibited distribution patterns similar to the macular carotenoids, with higher expression levels within the macular region compared to the periphery, while SR-BI and ABCA1 did not exhibit specific distribution patterns within the macula or RPE. Interestingly, LIPC, SR-BI's partner, accumulated specifically in the sub-foveal RPE. All three of these carotenoid transport proteins were found to be highly expressed in the RPE. These results offer valuable insights into the roles these proteins play in the formation of the macula lutea.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise Espectral Raman / Carotenoides / Microscopia Confocal / Epitélio Pigmentado da Retina / Macula Lutea / Microscopia de Fluorescência Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise Espectral Raman / Carotenoides / Microscopia Confocal / Epitélio Pigmentado da Retina / Macula Lutea / Microscopia de Fluorescência Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article