In-cell ligand binding was examined by monitoring the enhancement of PPAR alpha LBD expression as a function of the concentration of ligand in the growth media. The efficient expression and in-cell assay of the reported PPAR alpha LBD construct make it amenable to high through-put screening

assays in drug discovery programs. (C) 2009 Elsevier Inc. All rights reserved.”
“The secreted glycoprotein Dickkopf-1 (Dkk1), an antagonist of the Wnt/beta-catenin pathway, has been implicated in many neurodegenerative diseases. However, it is unknown whether Dkk1 is involved in the pathogenesis of Parkinson’s eFT-508 cell line disease (PD). In this study, we discovered that Dkk1 was induced in MPP+-treated PC12 cells and the increase of Dkk1 preceded PC12 cell loss. RhDkk1 aggravated the neurotoxicity of MPP+ in PC12 cells. Furthermore, the level of Dkk1 was correlated with the number of apoptotic PC12 cells. The apoptosis could be decreased by Dkk1-siRNA in MPP+-induced PC12 cells and Dkk1-siRNATegulated the expression of beta-catenin and p-Ser9-GSK-3 beta in MPP+-induced PC12 cells. LiCl (an inhibitor of GSK-3 beta) also rescued the loss of PC12 cell viability and the apoptosis induced by MPP+. These data suggest that the induction of Dkk1 contributes to the MPP+-induced neurotoxicity in PC12 cells via

inhibition of the canonical Wnt pathway and Dkk1 antagonists which could rescue the Wnt pathway might be neuroprotective in PD. (C) 2012 Elsevier Ltd. All rights reserved.”
“Midkine (MDK) belongs to a class of heparin-binding growth factors and is highly expressed in a number of cancers. MDK is a cysteine-rich 13 Silmitasertib cost kDa protein containing five disulfide bonds. In this study, we expressed recombinant human MDK (rhMDK) in Escherichia coli Origami 2 (DE3) strain, which carries a (trxB(-)/gor(522-)) double mutation. Soluble rhMDK was expressed at a high-level in this strain and the protein was purified by a two-step purification using heparin affinity and gel filtration chromatography. Seven milligrams of rhMDK with high purity was obtained from a 3 L culture. All 10 cysteines

were confirmed to be engaged in correct disulfide bond linkages by mass spectrometry analysis. Activity of purified rhMDK was confirmed by a neurite outgrowth assay using rat cerebellar granule cells. Active rhMDK is MK-8776 molecular weight a critical reagent for cancer drug discovery studies. (C) 2009 Elsevier Inc. All rights reserved.”
“The nucleus accumbens shell (AcbSh) and the lateral hypothalamus (LH) are both involved in the control of food intake. Activation of GABA(A) receptors or blockade of AMPA and kainate receptors within the AcbSh induces feeding, as does blockade of GABAA receptors or activation of NMDA receptors in the LH. Further, evidence suggests that feeding induced via the AcbSh can be suppressed by LH inhibition. However, it is unclear if this suppression is specific to feeding.