Advanced glycation end (AGE) product modification of laminin downregulates Kir4.1 in retinal Müller cells

PLoS One. 2018 Feb 23;13(2):e0193280. doi: 10.1371/journal.pone.0193280. eCollection 2018.

Abstract

Diabetic retinopathy (DR) is a major cause of adult blindness. Retinal Müller cells maintain water homeostasis and potassium concentration via inwardly rectifying Kir4.1 channels. Accumulation of advanced glycation end products (AGEs) is a major pathologic event in DR. While diabetes leads to a decrease in the Kir4.1 channels, it remains unknown whether AGEs-linked to the basement membrane (BM) affect normal Kir4.1 channels. For this study, we hypothesized that AGE-modification of laminin is detrimental to Kir4.1 channels, therefore, disrupting Müller cell function. The AGE-modified laminin-coated substrates were prepared by incubating Petri-dishes with laminin and methylglyoxal for seven days. The rat Müller cells (rMC-1) were propagated on AGE-modified laminin, and Kir4.1 expression and function were evaluated. Quantification of AGEs using ELISA revealed a dose-dependent increase in methylglyoxal-hydro-imidazolone adducts. The rMC-1 propagated on AGE-modified laminin demonstrated a decrease in Kir4.1 levels in immunofluorescence and western blot studies and a decrease in the Kir4.1 channel function. Kir4.1 decrease on AGE-modified laminin resulted in a disorganization of an actin cytoskeleton and disruption of α-dystroglycan-syntrophin-dystrophin complexes. Our studies suggest that AGE-modification of laminin is detrimental to Kir4.1 channels. By studying the role of AGEs in Kir4.1 channels we have identified a novel mechanism of Müller cell dysfunction and its subsequent involvement in DR.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cell Line
  • Diabetic Retinopathy / metabolism*
  • Diabetic Retinopathy / pathology
  • Ependymoglial Cells / metabolism*
  • Ependymoglial Cells / pathology
  • Glycation End Products, Advanced / chemistry
  • Glycation End Products, Advanced / metabolism*
  • Glycation End Products, Advanced / pharmacology
  • Laminin / chemistry
  • Laminin / metabolism*
  • Laminin / pharmacology
  • Potassium Channels, Inwardly Rectifying / biosynthesis*
  • Rats
  • Retina / metabolism*
  • Retina / pathology

Substances

  • Glycation End Products, Advanced
  • Kcnj10 (channel)
  • Laminin
  • Potassium Channels, Inwardly Rectifying