Connections between apoptosis pathways, endoplasmic reticulum stress and autophagy...
| Grant number: | 18/50004-6 |
| Support type: | Regular Research Grants |
| Duration: | August 01, 2018 - July 31, 2020 |
| Field of knowledge: | Health Sciences - Pharmacy |
| Cooperation agreement: | Texas Tech University |
| Mobility Program: | SPRINT - Projetos de pesquisa - Mobilidade |
| Principal Investigator: | Joilson de Oliveira Martins |
| Grantee: | Joilson de Oliveira Martins |
| Principal investigator abroad: | Naima Moustaid-Moussa |
| Institution abroad: | Texas Tech University (TTU), United States |
| Home Institution: | Faculdade de Ciências Farmacêuticas (FCF). Universidade de São Paulo (USP). São Paulo , SP, Brazil |
| Associated research grant: | 17/11540-7 - Investigating the role of insulin in the presence of allergic pulmonary inflammation in diabetic and healthy mice, AP.R |
Abstract
Obesity is a complex disease that increases mortality and associated comorbities such as diabetes and cardiovascular diseases. One of the critical pathways involved in obesity is the Renin Angiotensin System (RAS) which is classically known to regulate blood pressure and fluid balance is also expressed in adipose tissue. RAS contributes to inflammation in obesity and diabetes and is often linked to dysfunctions in cellular processes. These include the endoplasmic reticulum (ER) stress and autophagy, which are not well understood. We hypothesize that RAS contributes to metabolic diseases-associated inflammation through dysregulated ER stress and autophagy in adipocytes and immune cells (macrophages). We will test this hypothesis using mice overexpressing RAS specifically in the adipose tisssie to determine changes in these cellular processes. Additionally, we will investigate the mechanisms mediating these effects using adipocytes and cultured macrophages. Further, since adipose tissue is also composed of immune cells, it is critical to investigate the interactions between adipocytes and macrophages to better understand how they affect diabetes and obesity. Our proposal will help identify new potential targets for reducing RAS-induced obesity and related metabolic diseases. Importantly the foundation for the proposed research is based on strong established and complementary expertise and published work by the TTU (obesity/adipose tissue and USP (immunology partnering teams. (AU)