Glycogen storage in the human retinal pigment epithelium: A comparative study of diabetic and non-diabetic donors

Cristina Hernández, Marta Garcia-Ramírez, Mar García-Rocha, Cristina Saez-López, Ángela M. Valverde, Joan J. Guinovart, Rafael Simó

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10 Citations (Scopus)

Abstract

Liver and muscle glycogen content is reduced in diabetic patients but there is no information on the effect of diabetes on the glycogen content in the retinal pigment epithelium (RPE). The main aim of the study was to compare the glycogen content in the RPE between diabetic and non-diabetic human donors. Glycogen synthase (GS) and glycogen phosphorylase (GP), the key enzymes of glycogen metabolism, as well as their isoforms, were also assessed. For this purpose, 44 human postmortem eye cups were included (22 from 11 type 2 diabetic and 22 from 11 non-diabetic donors matched by age). Human RPE cells cultured in normoglycemic and hyperglycemic conditions were also analyzed. Glycogen content as well as the mRNA, protein content and enzyme activity of GS and GP were determined. In addition, GS and GP isoforms were characterized. In the RPE from diabetic donors, as well as in RPE cells grown in hyperglycemic conditions, the glycogen content was increased. The increase in glycogen content was associated with an increase in GS without changes in GP levels. In RPE form human donors, the muscle GS isoform but not the liver GS isoform was detected. Regarding GP, the muscle and brain isoform of GP but not the liver GP isoform were detected. We conclude that glycogen storage is increased in the RPE of diabetic patients, and it is associated with an increase in GS activity. Further studies aimed at determining the role of glycogen deposits in the pathogenesis of diabetic retinopathy are warranted. © 2014 Springer-Verlag.
Original languageEnglish
Pages (from-to)543-552
JournalActa Diabetologica
Volume51
Issue number4
DOIs
Publication statusPublished - 1 Jan 2014

Keywords

  • Diabetes
  • Glycogen
  • Glycogen phosphorilase
  • Glycogen synthase
  • Retina

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