Alpha-melanocyte stimulating hormone preserves islet graft survival through down-regulation of Toll-like receptors

Transplant Proc. 2012 May;44(4):1086-90. doi: 10.1016/j.transproceed.2012.02.018.

Abstract

The induction of Toll-like receptors (TLRs) in β cells is involved in β-cell death and graft rejection after transplantation. This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLRs. To test the effect of α-MSH on TLR regulation, we first isolated pancreatic islets from rats pretreated with/without α-MSH and assayed inflammatory cytokines and insulin release, and measured the expression of TLRs. Pancreatic islets were transplanted into the kidney capsule of a diabetes mellitus (DM) mouse with and without prior injection of α-MSH. The blood glucose levels were measured and TLR4 expression in transplanted kidney tissue was assessed. Islet morphology, including size and total mass, was improved in the α-MSH group compared to the control group. The expression of TLRs as well as nitric oxide and monocyte chemoattractant protein 1 production were decreased in islets isolated from α-MSH-treated rats. In DM mice, the normoglycemic ratio was higher in the α-MSH-treated group than in the sham group. Moreover, the high levels of TLR4 expression observed in DM kidney tissue were significantly decreased in islet-transplanted tissue with α-MSH. This study showed that α-MSH protects pancreatic islets from cell death and dysfunction through downregulation of TLRs. In conclusion, α-MSH could contribute to improved islet graft survival and function in pancreatic islet transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Chemokine CCL2 / metabolism
  • Cytokines / metabolism
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / immunology
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / surgery*
  • Diabetes Mellitus, Type 1 / chemically induced
  • Diabetes Mellitus, Type 1 / immunology
  • Diabetes Mellitus, Type 1 / metabolism
  • Diabetes Mellitus, Type 1 / surgery*
  • Down-Regulation
  • Graft Survival / drug effects*
  • Inflammation Mediators / metabolism
  • Injections, Intraperitoneal
  • Insulin / metabolism
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / immunology
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / surgery*
  • Islets of Langerhans Transplantation*
  • Male
  • Mice
  • Mice, Nude
  • Nitric Oxide / metabolism
  • Rats
  • Rats, Inbred Lew
  • Toll-Like Receptors / drug effects*
  • Toll-Like Receptors / metabolism
  • alpha-MSH / administration & dosage
  • alpha-MSH / pharmacology*

Substances

  • Blood Glucose
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Cytokines
  • Inflammation Mediators
  • Insulin
  • Toll-Like Receptors
  • Nitric Oxide
  • alpha-MSH