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Multi-User equipment approved in grant 20/04159-8: spectrophotometer Synergy

Grant number: 21/10469-2
Support Opportunities:Multi-user Equipment Program
Duration: November 01, 2021 - October 31, 2028
Field of knowledge:Biological Sciences - Physiology - Physiology of Organs and Systems
Principal Investigator:William Tadeu Lara Festuccia
Grantee:William Tadeu Lara Festuccia
Host Institution: Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
Associated research grant:20/04159-8 - mTORC2 and mTORC1 biology and involvement in steatosis development and progression to steatohepatitis and hepatocellular carcinoma, AP.TEM
As informações de acesso ao Equipamento Multiusuário são de responsabilidade do Pesquisador responsável
EMU web page: Página do Equipamento Multiusuário não informada
Type of equipment:Processos Biológicos - Caracterização - Leitores de placas
Caracterização de Materiais - Imageamento - Ótico
Manufacturer: Fabricante não informado
Model: Modelo não informado


Evidence gathered in the last decades suggests that lipotoxicity and inflammation, through still not completed defined molecular mechanisms, are the main factors connecting adipose tissue dysfunction to the development nonalcoholic fatty liver disease (NAFLD), a group of liver diseases that comprises from a simple hepatic steatosis (NAFL) to more severe steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma (HCC). We propose herein to molecularly characterize mTORC1 and mTORC2 biology in hepatocytes and macrophages with a special emphasis in their involvement in the development of NAFL and its progression to NASH and HCC. For this, we will perform hepatocyte and macrophage mTORC1 (Raptor) and mTORC2 (Rictor) gain and loss of function experiments in vitro in primary cells and in vivo in two different mouse models of NAFLD induced either genetically through hepatocyte deletion of PTEN or through the intake of a high-fat, high-cholesterol, high-sucrose, high-fructose diet associated to weekly injections of a carcinogen, denominated altogether as diet-induced NAFLD (DIN). By employing imaging techniques, molecular biology tools and metabolic assays combined with powerful state-of-the-art OMICS (lipidomics, phosphoproteomics, acetylomics and transcriptomics), we will investigate the role of mTORC1 and mTORC2 in the regulation of the following inter-related processes in the NAFL-NASH-HCC progression: lipid metabolism and lipotoxicity; glucose homeostasis and glucotoxicity; endoplasmic reticulum and oxidative stress; inflammation; mitochondrial and peroxisomal oxidative metabolism, reactive oxygen species production and function, autophagy, epigenetics, DNA mutagenesis and repair, and tumorigenesis. (AU)

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