Suppressor of cytokine signaling-1 ameliorates expression of MCP-1 in diabetic nephropathy

Am J Nephrol. 2010;31(5):380-8. doi: 10.1159/000286559. Epub 2010 Mar 19.

Abstract

Background: Janus kinase (JAK)/signal transducers and activators of transcription (STAT) contribute to diabetic nephropathy. Suppressor of cytokine signaling-1 (SOCS-1) is one of the negative feedback regulators of JAK/STAT signaling. This study investigated the effect of SOCS-1 on the JAK/STAT pathway and MCP-1 expression in diabetic nephropathy.

Methods: Streptozotocin-induced diabetic mice received pEF-FLAG-I/mSOCS-1 plasmid or pEF-FLAG-I vector for 4 weeks and were compared with age-matched nondiabetic mice. Functional and pathologic markers, expression of monocyte chemoattractant protein-1 (MCP-1) and TGF-beta1 and phosphorylation of STAT1 and STAT3 were assessed. The effect of SOCS-1 on the expression of MCP-1 in mesangial cells under high glucose conditions was also examined.

Results: Urine albumin excretion and renal hypertrophy were alleviated in diabetic mice by overexpression of SOCS-1. The expression of TGF-beta1 and MCP-1 and the activation of STAT1 and STAT3 were significantly inhibited in diabetic kidney by gene delivery of SOCS-1. In cultured mesangial cells, overexpression of SOCS-1 markedly suppressed high glucose-induced MCP-1 expression.

Conclusions: This study suggests that SOCS-1 may attenuate renal damage by ameliorating MCP-1 expression and regulation of the phosphorylation of JAK/STAT in diabetic mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Chemokine CCL2 / metabolism*
  • Diabetes Mellitus, Experimental / blood*
  • Diabetes Mellitus, Experimental / therapy
  • Diabetic Nephropathies / blood*
  • Diabetic Nephropathies / therapy*
  • Humans
  • Immunohistochemistry / methods
  • Male
  • Mice
  • Phosphorylation
  • STAT1 Transcription Factor / metabolism
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling Proteins / metabolism*
  • Transforming Growth Factor beta1 / biosynthesis

Substances

  • Blood Glucose
  • CCL2 protein, human
  • Ccl2 protein, mouse
  • Chemokine CCL2
  • SOCS1 protein, human
  • STAT1 Transcription Factor
  • Socs1 protein, mouse
  • Stat1 protein, mouse
  • Suppressor of Cytokine Signaling 1 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Transforming Growth Factor beta1