Haefliger JA Rohner-Jeanrenaud F Caille D Charollais A Meda P Allagnat F 2013 Channels formed by the gap junction protein Connexin36 (CX36) contribute to the proper control of insulin secretion. We previously demonstrated that chronic exposure to glucose decreases Cx36 levels in insulin-secreting cells in vitro. Here, we investigated whether hyperglycemia also regulates Cx36 in vivo. Using a model of continuous glucose infusion in adult rats, we showed that prolonged (24-48 h) hyperglycemia reduced the Cx36 gene Gjd2 mRNA levels in pancreatic islets. Accordingly, prolonged exposure to high glucose concentrations also reduced the expression and function of Cx36 in the rat insulin-producing INS-1E cell line. The glucose effect was blocked after inhibition of the cAMP/PKA pathway and was associated with an overexpression of the inducible cAMP early repressor ICER-1/ICER-1γ, which binds to a functional cAMP-response element in the promoter of the Cx36 gene Gjd2. The involvement of this repressor was further demonstrated using an antisense strategy of ICER-1 inhibition, which prevented glucose-induced downregulation of Cx36. The data indicate that chronic exposure to glucose alters the in vivo expression of Cx36 by the insulin-producing β-cells through ICER-1/ICER-1γ overexpression. This mechanism may contribute to the reduced glucose sensitivity and altered insulin secretion, which contribute to the pathophysiology of diabetes. application/pdf https://sonar.ch/global/documents/257093 eng info:eu-repo/semantics/altIdentifier/doi/10.1530/JME-13-0054 info:eu-repo/semantics/altIdentifier/pmid/23613279 info:eu-repo/semantics/openAccess Journal of molecular endocrinology. - 2013 ICER-1 connexin36 gap junctions glucose Animals Blood Glucose Cell Line, Tumor Connexins Cyclic AMP Response Element Modulator Gene Expression Regulation Glucose Hyperglycemia Islets of Langerhans Male Rats Hyperglycemia downregulates Connexin36 in pancreatic islets via the upregulation of ICER-1/ICER-1γ. http://purl.org/coar/resource_type/c_6501