Expression of adiponectin and its receptors in type 1 diabetes mellitus in human and mouse retinas

Mol Vis. 2013 Aug 4:19:1769-78. Print 2013.

Abstract

Purpose: Recent studies have suggested that adiponectin (APN) is associated with several retinal diseases. We studied the expression of APN and its receptors (AdipoRs) in the human retina and in a mouse model of type 1 diabetes mellitus (T1DM).

Methods: Human eyeball specimens were obtained from the Chongqing Eye Bank. eNOS-knockout (eNOS⁻/⁻) mice were randomly divided into a T1DM group and a control group. The T1DM model was induced with an intraperitoneal injection of streptozotocin. To locate the AdipoRs in the retina, immunofluorescence was performed. Total APN protein and RNA were extracted from the neural retina and the retinal pigment epithelium (RPE)-choroid complex, and the APN protein was detected with enzyme-linked immunosorbent assay (ELISA). The mRNA and the protein of AdipoRs in the retina were detected with qRT-PCR and western blotting, respectively. The unpaired Student t test was used to assess the significance between the T1DM and the control groups, with p<0.05 regarded as statistically significant.

Results: APN, AdipoR1, and AdipoR2 were identified in the neural retina and in the RPE-choroid of humans and mice. AdipoR1 was found in the internal limiting membrane and in the outer segments of the photoreceptors in human and mouse retinas, whereas no noticeable AdipoR2 expression was seen in the retinal frozen sections of human and mouse eyes. Compared to the control group, APN and AdipoR1 expression in the retina was elevated in the T1DM group, but AdipoR2 expression remained unchanged.

Conclusions: We demonstrated that APN, AdipoR1, and AdipoR2 exist in human and mouse retinas and that retinal APN and AdipoR1 protein levels are elevated in T1DM mice, implying that the APN-AdipoR1 axis may be activated in the diabetic retina. In contrast, AdipoR2 appears to play a minor role in this pathological process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / genetics*
  • Adiponectin / metabolism
  • Adult
  • Aging / blood
  • Animals
  • Blood Glucose / metabolism
  • Choroid / metabolism
  • Choroid / pathology
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / genetics*
  • Female
  • Fluorescent Antibody Technique
  • Gene Expression Regulation
  • Humans
  • Male
  • Mice
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Adiponectin / genetics*
  • Receptors, Adiponectin / metabolism
  • Retina / metabolism*
  • Retina / pathology
  • Retinal Pigment Epithelium / metabolism
  • Retinal Pigment Epithelium / pathology

Substances

  • Adiponectin
  • Blood Glucose
  • RNA, Messenger
  • Receptors, Adiponectin