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Volume 6, Issue 8(Suppl) J Obes Weight Loss Ther 2016
ISSN: 2165-7904 JOWT, an open access journal
Page 53
Notes:
Euro Obesity 2016
October 10-12, 2016
conferenceseries.com
7th Obesity & Endocrinology
Specialists Congress
October 10-12, 2016 Manchester, UK
Role of macrophage in the regulation of hepatocyte fat metabolism
Susmita Chandra
Indian Institute of Chemical Biology-CSIR, India
Macrophage secretory products contribute to the pathogenesis of chronic liver diseases by sensing danger signals from damaged
cellsunder pathogenic inflammatory conditions like fatty liver or infection. Liver resident Kupffer cells activate inflammosome
and caspase-1 to proteolyte cytokines IL-1β and IL-18. The endogenous interleukin-1 receptor antagonist (IL-1Ra), secreted
by activated monocytes and macrophages binds to IL-1 receptors & prevents IL-1 from sending a signal to that cell. Our study
is designed to understand the molecular basis of inflammatory condition developed during fatty liver diseases which regulates
hepatocyte fat metabolism. Cultured human THP-1 cells were differentiated into macrophages and stimulated by LPS to treat with
BSA-Palmitate. The cytokines in THP-1 conditioned media (CM) were profiled by ELISA or HPLC. HepG2 cells were treated with
the CM & BSA-Palmitate. Fatty acid oxidation (FAO) was measured in HepG2. Fat deposition was qualitatively determined by Oil
Red O and Triglyceride (TG) accumulation assay. Total RNA from HepG2 cells were isolated to profile gene expressions by RTqPCR.
Some expressed proteins were determined by qPCR and immune-blotting. Recombinant IL-1 decreased FAO which was dose-
dependently reversed by IL-1Ra in HepG2 cells. IL-1Ra enriched CM from LPS stimulated THP-1 macrophage increased rate of FAO
and prevented IL-1 dependent decrease in FAO. The intracellular triglyceride levels were accordingly modulated. Thus, IL-1Ra has
an important role in controlling the fat accumulation and its metabolism in HepG2 cells. Recombinant IL-1Ra can play a potential
role in blocking inflammasome induced IL-1β dependent liver inflammation and combat the inflammatory condition developed
during fatty liver diseases.
Biography
Susmita Chandra has completed her PhD during 2011 from Jadavpur University, Kolkata, India. She is working as a Post-doctoral Fellow at Cell Biology and Physiology
Division of Indian Institute of Chemical Biology. She has 10 published papers in reputed journals and has presented her research contribution in a number of national and
international conferences. Her previous and current research contribution encompasses mainly different areas of drug development studies.
Susmita Chandra, J Obes Weight Loss Ther 2016, 6:8(Suppl)