Abstract
Type 1 diabetes develops when most insulin-producing β cells of the pancreas are killed by an autoimmune attack. The in vivo conditions modulating the sensitivity and resistance of β cells to this attack remain largely obscure. Here, we show that connexin 36 (Cx36), a trans-membrane protein that forms gap junctions between β cells in the pancreatic islets, protects mouse β cells against both cytotoxic drugs and cytokines that prevail in the islet environment at the onset of type 1 diabetes. We documented that this protection was at least partially dependent on intercellular communication, which Cx36 and other types of connexin channels establish within pancreatic islets. We further found that proinflammatory cytokines decreased expression of Cx36 and that experimental reduction or augmentation of Cx36 levels increased or decreased β cell apoptosis, respectively. Thus, we conclude that Cx36 is central to β cell protection from toxic insults.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Alloxan / pharmacology
-
Alloxan / toxicity
-
Animals
-
Apoptosis / drug effects
-
Cell Communication
-
Cellular Microenvironment
-
Connexins / antagonists & inhibitors
-
Connexins / deficiency
-
Connexins / genetics
-
Connexins / physiology*
-
Diabetes Mellitus, Experimental / chemically induced
-
Diabetes Mellitus, Experimental / metabolism
-
Diabetes Mellitus, Experimental / pathology
-
Diabetes Mellitus, Experimental / prevention & control*
-
Gap Junction delta-2 Protein
-
Gap Junctions / physiology
-
Gene Dosage
-
Insulin / genetics
-
Interferon-gamma / toxicity
-
Interleukin-1beta / toxicity
-
Islets of Langerhans / drug effects
-
Islets of Langerhans / metabolism
-
Islets of Langerhans / pathology*
-
Mice
-
Mice, Inbred C57BL
-
Mice, Knockout
-
Mice, Transgenic
-
Nitric Oxide / biosynthesis
-
Promoter Regions, Genetic
-
RNA Interference
-
RNA, Small Interfering / pharmacology
-
Rats
-
Recombinant Fusion Proteins / physiology
-
Streptozocin / pharmacology
-
Streptozocin / toxicity
-
Tumor Necrosis Factor-alpha / toxicity
Substances
-
Connexins
-
Insulin
-
Interleukin-1beta
-
RNA, Small Interfering
-
Recombinant Fusion Proteins
-
Tumor Necrosis Factor-alpha
-
Nitric Oxide
-
Streptozocin
-
Alloxan
-
Interferon-gamma