Literature DB >> 14502241

Bifunctional apoptosis inhibitor (BAR) protects neurons from diverse cell death pathways.

W Roth1, P Kermer, M Krajewska, K Welsh, S Davis, S Krajewski, J C Reed.   

Abstract

The bifunctional apoptosis regulator (BAR) is a multidomain protein that was originally identified as an inhibitor of Bax-induced apoptosis. Immunoblot analysis of normal human tissues demonstrated high BAR expression in the brain, compared to low or absent expression in other organs. Immunohistochemical staining of human adult tissues revealed that the BAR protein is predominantly expressed by neurons in the central nervous system. Immunofluorescence microscopy indicated that BAR localizes mainly to the endoplasmic reticulum (ER) of cells. Overexpression of BAR in CSM 14.1 neuronal cells resulted in significant protection from a broad range of cell death stimuli, including agents that activate apoptotic pathways involving mitochondria, TNF-family death receptors, and ER stress. Downregulation of BAR by antisense oligonucleotides sensitized neuronal cells to induction of apoptosis. Moreover, the search for novel interaction partners of BAR identified several candidate proteins that might contribute to the regulation of neuronal apoptosis (HIP1, Hippi, and Bap31). Taken together, the expression pattern and functional data suggest that the BAR protein is involved in the regulation of neuronal survival.

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Year:  2003        PMID: 14502241     DOI: 10.1038/sj.cdd.4401287

Source DB:  PubMed          Journal:  Cell Death Differ        ISSN: 1350-9047            Impact factor:   15.828


  19 in total

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8.  Preliminary structural studies on the leucine-zipper homology region of the human protein Bap31.

Authors:  Takashi Mukasa; Eugenio Santelli; John C Reed; Jaime Pascual
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-03-12

9.  Cytosolic prion protein is the predominant anti-Bax prion protein form: exclusion of transmembrane and secreted prion protein forms in the anti-Bax function.

Authors:  David T S Lin; Julie Jodoin; Michaël Baril; Cynthia G Goodyer; Andréa C Leblanc
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10.  Transcription regulation of caspase-1 by R393 of HIPPI and its molecular partner HIP-1.

Authors:  M Banerjee; M Datta; P Majumder; D Mukhopadhyay; N P Bhattacharyya
Journal:  Nucleic Acids Res       Date:  2009-11-24       Impact factor: 16.971

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