| Grant number: | 11/51701-3 |
| Support Opportunities: | Research Grants - Young Investigators Grants |
| Start date: | June 01, 2012 |
| End date: | May 31, 2016 |
| Field of knowledge: | Biological Sciences - Physiology - Physiology of Organs and Systems |
| Principal Investigator: | Paula Bresciani Martins de Andrade |
| Grantee: | Paula Bresciani Martins de Andrade |
| Host Institution: | Pró-Reitoria de Extensão e Assuntos Comunitários. Universidade Cruzeiro do Sul (UNICSUL). São Paulo , SP, Brazil |
| City of the host institution: | São Paulo |
| Associated scholarship(s): | 15/10122-1 - Oxygen consumption in 3T3-L1 pre-adipocytes and the effect of palmitoleic acid,
BP.IC 12/10525-0 - MITOCHONDRIAL FUNCTION DURING WHITE ADIPOSE TISSUE (WAT) ADIPOGEESIS: THE EFFECT OF FATTY ACIDS, BP.JP |
Abstract
Mitochondrial biogenesis and metabolism are involved in the regulation of white adipose tissue functioning, such as adipogenesis, lipid and carbohydrate metabolism, preadipocyte proliferation, adipocyte dedifferentiation and triglyceride accumulation. However, this issue is still under debate. The goal of this project is to investigate the effect of saturated and insaturated fatty acids (FA) on mitochondrial metabolism and their implication on preadipocytes differentiation into mature adipocytes (adipogenesis). The clonal cell line 3T3-L1 will be employed, as well as primary preadipocytes driven to the differentiation into mature adipocytes. These cells will be treated in different periods of cell culture with the following FA: palmitic (C16:0), palmitoleic (C16:1 omega-7), linoleic (C18:2, omega-6), eicosapentaenoic (EPA, C20:5 omega-3) and docosahexaenoic (DHA, C22:6 omega-3). The following parameters will be evaluated: (1) mitochondrial biogenesis and metabolism, (2) adipogenic potential of primary preadipocytes and 3T3-L1 cells, (3) peroxisome proliferator-activated receptor (PPAR)-y coactivator (PGC)-1a, transcription factor A (TFAM), carnitine palmitoyl transferase 1 (CPT1), nuclear respiratory factor 1 (NRF1), uncoupling protein 2 (UCP2) and manganese superoxide dismutase (MnSOD) gene expression, and (4) mitochondrial proteomics analysis during adipogenesis. The following techniques will be employed: fluorimetry, lumínescence, real time RT-PCR, western blotting and proteomics. With the results obtained we will contribute to the elucidation of the role of mitochondria and different FA in adipogenesis. (AU)
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