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Evaluation of non-alcoholic fatty liver disease (NAFLD) susceptibility dependent of truncated neurotrophic tyrosine receptor kinase 2 (NTRK2.T1) in liver of C57BL/6J mice conditionally over-expressing and FVB/N conditionally supressing this receptor


Non-Alcahoolic Fatty Liver Disease prevalence is around one-fourth worldwide, being considered the hepatic component of metabolic syndrome. It is characterized by fat accumulation in liver (steatosis) and can develop to non-alcoholic steato-hepatitis (NASH). Brain derived neurotrophic factor (BDNF) signaling cascade requires neurotrophic receptor tyrosine kinase (NTRK2), mediating neuron survival, differentiation and plasticity, and in brain, this pathway is essential for appetite control.In liver, this signaling cascade represses oxidation/exportation of fat acids, leading to steatosis.In previous work, our group identified a 20x higher expression of NTRK2 in liver of FVB/N mouse strain, compared to C57Bl/6J strain. When challenged with high fat diet, FVB/N animals presented severe steatosis compared to C57Bl/6J.We also identified that truncated version of NTRK2 receptor (NTRK2.T1) is predomanately expressed in FVB/N hepatocytes.Considering the pronounced effect of BDNF/NTRK2 pathway in energy balance and the crescent interest in using agonists to treat obesity, via anorexigenic effects in central nervous system, it is important to evaluate this pathway role in development of NAFLD. Despite our previous results show a key role for NTRK2.T1 in this process in vitro, animals models manipulating NTRK2.T1 expression in liver are of great value to further understand NAFLD development. (AU)

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(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
GAISLER-SILVA, FERNANDA; CRUZ JUNHO, CAROLINA VICTORIA; FREDO-DA-COSTA, IZABELLE; CHRISTOFFOLETE, MARCELO AUGUSTO; CARNEIRO-RAMOS, MARCELA SORELLI. Diet-induced Obesity Differentially Modulates Cardiac Inflammatory Status in the C57 and FVB Mouse Strains. CURRENT MOLECULAR MEDICINE, v. 22, n. 4, p. 9-pg., . (15/02052-3, 15/19107-5, 18/07811-8, 19/11077-0)

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