Therefore, we aimed to clarify the mechanisms by which DCA modulates the miR-21 signalling pathway and contributes to apoptosis in primary rat hepatocytes. Cells were incubated with 25-100 μM DCA for 4 to 48 h. www.selleckchem.com/products/LDE225(NVP-LDE225).html Cell death, viability and caspase-3

activity were determined by the ApoTox-GloTM Triplex Assay. miR-21 expression was evaluated by qRT-PCR. Programmed cell death 4 (PDCD4) and phosphatase and tensin homolog (PTEN), two miR-2 1 targets, as well as NF-kB, IkB and caspases were analysed by immunobloting. NF-kB activation was evaluated by NF-kB subcellular localization. For functional analyses, miR-21, NF-kB and caspase-2 were modulated using specific genetic and pharmacologic inhibitors or activators. Our results show that the miR-21 pathway is modulated

by DCA in a dose-dependent manner. 100 μM DCA already significantly induced caspase2/-3 activities and apoptosis, while reducing cellular viability. In parallel, miR-21 expression was inhibited with a concomitant increase in PDCD4 and PTEN protein levels. In addition, DCA inhibited NF-kB expression and activity, NF-kB/IkB ratio and NF-қB nuclear expression, in a similar pattern to miR-21 inhibition. NVP-BEZ235 purchase In fact, miR-21 overexpression impaired the ability of DCA to induce PDCD4 and PTEN expression, as well as apoptosis, but had little effect on NF-қB activation. Importantly, after ectopic activation of NF-қB, DCA was less capable of repressing miR-2 1, and its cytotoxicity was decreased; inhibiting NFkB using BAY 11-7085 had opposite effects. Finally, caspase-2 inhibition by zVDVAD-fmk resulted in a significant decrease in DCA-repressed NF-қB and -induced cell death. In conclusion, DCA appears to modulate the miR-2 1 pro-apoptotic pathway via activation of caspase-2 上海皓元医药股份有限公司 and downstream inhibition of NFkB. A better understanding of the mechanisms by which DCA impacts on cell death may allow for the development of new therapeutic tools to treat apoptosis-related pathologies. (Supported by PTDC/SAU-OSM/1 02099/2008, PTDC/SAU ORG/111 930/2009, Pest-OE/SA U/ / U I401 3/2011, SFRH/BD/88212/2012 (P. M. R. ),

SFRH/BD/91119/2012 (M. B. A) and SFRH/BD/60521/2009 (D. M. S. F) from FCT, Lisbon). Disclosures: The following people have nothing to disclose: Pedro M. Rodrigues, Marta B. Afonso, Duarte M. Ferreira, Pedro M. Borralho, Cecίlia M. Rodrigues, Rui E. Castro Bile acids are retained during cholestatic liver disease and and contribute to ongoing pathology by inducing hepatocyte apoptosis. Bile acid induced apoptosis proceeds through a phosphoinositide-3-kinase gamma/endoplasmic reticulum stress/CJun-NH3 terminal kinase (JNK) mitochondrially dependent pathway (Hohenester S et al J Hepatol. 2010; 53: 918; Johnston A et al Am J Physiol Gastrointest Liver, 2011; 301: G385). Some bile acids activate the delta isoform of protein kinase C (PKC) in hepatocytes, but the role of this kinase in bile acid apoptosis is unknown. AIM: To determine the role of PKC delta in bile acid apoptosis.