Identification and localization of reactive oxygen species during nutrient-induced insulin secretion: role of NADPH oxidase.

• Grant number: 11/18993-0
• Support type: Scholarships in Brazil - Post-Doctorate
• Effective date (Start): February 01, 2012
• Effective date (End): August 31, 2015
• Field of knowledge: Biological Sciences - Physiology - Physiology of Organs and Systems
• Principal researcher: Angelo Rafael Carpinelli
• Grantee: Leticia Prates Roma
• Home Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated research grant: 09/51893-0 - The role of NAD(P)H oxidase in the molecular mechanisms of pancreatic beta cell physiology, AP.TEM
• Associated scholarship(s): 13/22830-5 - In vivo imaging of H2O2: characterization of the roGFP2-Orp1 mouse, BE.EP.PD

Abstract

In vivo and in vitro data provide evidences of oxygen reactive species (ROS) as one of the common factors between insulin resistance, decreased insulin secretion and diabetes. However, ROS are known to be important during cell signaling and other events such as proliferation, apoptosis and insulin secretion. Free Fatty acids (FFA) have a direct effect on pancreatic beta cell, controlling insulin secretion and cell viability. One of the important effects of FFA on beta cell is the activation of NADPH oxidase. The aim of this study is to investigate the role of ROS and NADPH oxidase on insulin secretion and beta cell dysfunction after exposure to nutrients. To test this, the following strategies will be used: 1) islets from control and knockout mice for gp91phox subunit (gp91 phox-/-) and 2) interference RNA to delete the p22 phox subunit in cell lines. Pancreatic islets and beta cells will be incubated with different glucose concentrations and FFA (palmitate and oleate) and infected with adenovirus/lentivirus expressing genetically encoded probes target to different compartments (mitochondria, cytoplasm, peroxissomes, endoplasmic reticulum) to measure oxidative stress in dynamic and real time experiments. Cell viability, changes in calcium , metabolism and signalling pathways will also be addressed. In addition, we will use an insulin resistance animal model (ob/ob) to analyze the importance of NADPH oxidase and ROS production on beta cell dysfunction. A better understanding of the role of NADPH oxidase e and FFA on ROS production, insulin secretion and signaling is of fundamental importance to elucidate the mechanisms of diabetes development.