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Human retinal pigment epithelial cells prefer proline as a nutrient and transport metabolic intermediates to the retinal side.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2017 Aug 04; Vol. 292 (31), pp. 12895-12905. Date of Electronic Publication: 2017 Jun 14. - Publication Year :
- 2017
-
Abstract
- Metabolite transport is a major function of the retinal pigment epithelium (RPE) to support the neural retina. RPE dysfunction plays a significant role in retinal degenerative diseases. We have used mass spectrometry with <superscript>13</superscript> C tracers to systematically study nutrient consumption and metabolite transport in cultured human fetal RPE. LC/MS-MS detected 120 metabolites in the medium from either the apical or basal side. Surprisingly, more proline is consumed than any other nutrient, including glucose, taurine, lipids, vitamins, or other amino acids. Besides being oxidized through the Krebs cycle, proline is used to make citrate via reductive carboxylation. Citrate, made either from <superscript>13</superscript> C proline or from <superscript>13</superscript> C glucose, is preferentially exported to the apical side and is taken up by the retina. In conclusion, RPE cells consume multiple nutrients, including glucose and taurine, but prefer proline, and they actively synthesize and export metabolic intermediates to the apical side to nourish the outer retina.<br /> (© 2017 by The American Society for Biochemistry and Molecular Biology, Inc.)
- Subjects :
- Animals
Biological Transport
Carbon Isotopes
Cell Polarity
Cells, Cultured
Citric Acid metabolism
Citric Acid Cycle
Coculture Techniques
Embryo, Mammalian cytology
Glucose metabolism
Humans
Kinetics
Metabolomics methods
Mice
Retina cytology
Retina enzymology
Retinal Pigment Epithelium cytology
Retinal Pigment Epithelium enzymology
Taurine metabolism
Tissue Culture Techniques
Proline metabolism
Retina metabolism
Retinal Pigment Epithelium metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1083-351X
- Volume :
- 292
- Issue :
- 31
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28615447
- Full Text :
- https://doi.org/10.1074/jbc.M117.788422