Targeting Estrogen Receptors to Protect Functional Beta-cell Mass in Diabetes

Tulane University Of Louisiana, New Orleans LA

Investigators

Linked publications, trials & patents

Abstract

DESCRIPTION (provided by applicant): This is the resubmission of the first competitive renewal of R01DK074970 Role of estrogen receptors in beta- cell survival and insulin secretion. Our laboratory was a pioneer in demonstrating that the female hormone 17¿-estradiol (E2) protects islet ¿-cells from apoptosis in vivo in mice. We have shown that E2 anti-apoptotic protection is mediated via extranuclear estrogen receptor (ER)s. We also reported that activation of these ERs enhances islet insulin biosynthesis and prevents islet lipotoxicity in vivo thus preventing ¿-cell failure in rodent models of type 2 diabetes. This competitive renewal focuses on the role of ERs in pancreatic islet engraftment during transplantation in insulin deficient diabetes. Pancreatic islet transplantation (PIT) is an important therapeutic approach in type 1 diabetes (T1D). However, the failure of islet revascularization and engraftment limits its widespread application. The transplanted islets exposed to multiple insults may be destroyed before revascularization occurs. Our new preliminary data suggest that ER activation permanently improves human islet engraftment during PIT in a mouse model of T1D via multiple mechanisms involving an acute suppression of islet graft hypoxia and apoptosis and an acute suppression of hyperglucagonemia. This is associated to a latter increase in islet revascularization and functional mass. In this application we propose to explore the contributions of the ER¿ in graft ¿-cells, recipient ¿-cells and endothelial cells to islet revascularization during PIT, using mice with conditional null alleles of ER¿ in these cells. We also propose to explore the synergy between estrogen and glucagon-like peptide-1 (GLP-1) in human islet survival and revascularization in a diabetic mouse model of PIT using a novel compound combining E2 and GLP-1 in a single molecule which allows the targeting of E2 where membrane GLP-1 receptors are present, the ¿-cells and the endothelial cells, and away from gynecological tissues.