(c) 2009 Elsevier Ltd. All rights reserved.”
“Neuregulin-1 beta (NRG-1 beta) is a growth factor with potent neuroprotective capacity. Growth-associated protein 43 (GAP-43) is expressed in dorsal root ganglion (DRG) neurons and an indicator of Flavopiridol in vivo neuronal survival in vitro. The purpose of present study is to evaluate the effects of NRG-1 beta on

GAP-43 expression in DRG neurons with excitotoxicity induced by glutamate (Glu) in vitro. The phosphatidylinositol 3-kinase (PI3K)/Akt and extracellular signal-regulated protein kinase 1/2 (ERK1/2) signaling pathways involved in these effects were also determined. Embryonic rat DRG neurons were treated with Glu in the absence or presence of NRG-1 beta and PI3K inhibitor LY294002 and/or

ERK1/2 inhibitor PD98059. After that, GAP-43 mRNA and GAP-43 protein levels were analyzed by real time-PCR and western blot assay, respectively. GAP-43 expression in situ was determined by immunofluorescent labeling. The results showed that the decreased GAP-43 levels induced Pevonedistat chemical structure by Glu could be partially reversed by the presence of NRG-1 beta. Inhibitors (LY294002, PD98059),either alone or in combination blocked the effects of NRG-1 beta. These data provide new insights of the actions of NRG-1 beta in sensory neurons. (c) 2013 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.”
“Aims: The main aims of this study were to construct a bivalent subunit vaccine containing flagellin flaA gene and flagellin flaB gene from Vibrio alginolyticus strain HY9901 and to explore the potential application of the fusion protein FlaA-(G4S)3-FlaB as a vaccine candidate for red snapper (Lutjanus sanguineus). Methods and Results: Flagellin gene flaA and flaB of V.similar to alginolyticus were linked by gene SOEing (gene splicing by overlap extension) technology. The expression of the fusion gene flaA-(G4S)3-flaB in Escherichia coli BL21(DE3) was confirmed

by SDS-PAGE. Western blot analysis showed that the fusion protein FlaA-(G4S)3-FlaB, which was purified by affinity chromatography on Ni-NTA resin, had positive reaction with mouse anti-FlaA serum and mouse anti-FlaB serum, respectively. The immunoprotection of FlaA-(G4S)3-FlaB as a bivalent subunit vaccine was investigated in red snapper model by enzyme-linked immunosorbent assay (ELISA) Ribonuclease T1 and challenge test. Red snapper vaccinated with FlaA-(G4S)3-FlaB produced specific antibodies and were highly resistant to infection by virulent V.similar to alginolyticus. Conclusions: The fusion gene flaA-(G4S)3-flaB from V.similar to alginolyticus strain HY9901 was cloned by gene SOEing and was expressed in E similar to coli. This fusion protein FlaA-(G4S)3-FlaB is a good protective antigen of V.similar to alginolyticus and should be considered as an effective vaccine candidate against infection by V.similar to alginolyticus in red snapper.