http://www.cnr.it/ontology/cnr/individuo/prodotto/ID4310
Nerve Growth Factor-dependent survival of CESS B cell line is mediated by increased expression and decreased degradation of MAPK Phosphatase 1 (Articolo in rivista)
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- Nerve Growth Factor-dependent survival of CESS B cell line is mediated by increased expression and decreased degradation of MAPK Phosphatase 1 (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1074/jbc.M305356200 (literal)
- Alternative label
Rosini P.1; De Chiara G.2; Bonini P.1; Lucibello M.2,3, Marcocci M.E.2; Garaci E.2; Cozzolino 1,2,3; Torcia M.G.1; (2004)
Nerve Growth Factor-dependent survival of CESS B cell line is mediated by increased expression and decreased degradation of MAPK Phosphatase 1
in Journal of biological chemistry (Online)
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- Rosini P.1; De Chiara G.2; Bonini P.1; Lucibello M.2,3, Marcocci M.E.2; Garaci E.2; Cozzolino 1,2,3; Torcia M.G.1; (literal)
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- Impact Factor 6.482 (literal)
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- 1= Department of Clinical Physiopathology, University of Florence, Florence, Italy;
2= Department of Experimental Medicine, University of Rome \"Tor Vergata\", Via di Tor Vergata 135, I-00133 Rome, Italy
3= Institute of Neurobiology and Molecular Medicine, National Research Council, Via del Fosso del Cavaliere 100, I-00133 Rome, Italy; (literal)
- Titolo
- Nerve Growth Factor-dependent survival of CESS B cell line is mediated by increased expression and decreased degradation of MAPK Phosphatase 1 (literal)
- Abstract
- The sIgG(+) lymphoblastoid B cell line CESS spontaneously produces a high amount of nerve growth factor (NGF) and expresses both high affinity (p140(Trk-A)) and low affinity (p75(NTR)) NGF receptors. Autocrine production of NGF maintains the survival of CESS cells through the continuous deactivation of p38 MAPK, an enzyme able to induce Bcl-2 phosphorylation and subsequent cytochrome c release and caspase activation. In this paper, we show that NGF induces transcriptional activation and synthesis of MAPK phosphatase 1 (MKP-1), a dual specificity phosphatase that dephosphorylates p38 MAPK, thus preventing Bcl-2 phosphorylation. Furthermore, NGF increases MKP-1 protein stability by preventing its degradation through the proteasome pathway. Following NGF stimulation, MKP-1 protein mainly localizes on mitochondria, suggesting an interaction with p38 MAPK in this compartment. Incubation of CESS cells with MKP-1-specific antisense oligonucleotides induces cell death, which was not prevented by exogenous NGF. By contrast, overexpression of native MKP-1, but not of its catalytically impaired form, inhibits apoptosis induced by NGF neutralization in CESS cells. Thus, the molecular mechanisms underlying the survival function of NGF in CESS B cell line predominantly consist in maintaining elevated levels of MKP-1 protein, which controls p38 MAPK activation. (literal)
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