Differential antiapoptotic effect of erythropoietin on undifferentiated and retinoic acid-differentiated SH-SY5Y cells

Erythropoietin (Epo) is known to have a significant role in tissues outside the hematopoietic system. In this work, we investigated the function of Epo in cells of neuronal origin subjected to differentiation. Treatment of SH-SY5Y cells with all-trans-retinoic acid (atRA) generated differentiated ne...

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Autor principal: Wenker, S.D
Otros Autores: Chamorro, M.E, Vota, D.M, Callero, M.A, Vittori, D.C, Nesse, A.B
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2010
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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024 7 |2 cas  |a erythropoietin, 11096-26-7; phosphatidylinositol 3 kinase, 115926-52-8; protein bcl 2, 219306-68-0; protein bcl xl, 151033-38-4; protein kinase B, 148640-14-6; retinoic acid, 302-79-4; 1-Phosphatidylinositol 3-Kinase, 2.7.1.137; Erythropoietin, Recombinant; Tretinoin, 302-79-4 
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030 |a JCEBD 
100 1 |a Wenker, S.D. 
245 1 0 |a Differential antiapoptotic effect of erythropoietin on undifferentiated and retinoic acid-differentiated SH-SY5Y cells 
260 |c 2010 
270 1 0 |m Wenker, S. D.; Departamento de Química Biológica, Universidad de Buenos Aires, Ciudad Universitaria, Ciudad Autónoma de Buenos Aires C1428EHA, Argentina; email: swenker@qb.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Erythropoietin (Epo) is known to have a significant role in tissues outside the hematopoietic system. In this work, we investigated the function of Epo in cells of neuronal origin subjected to differentiation. Treatment of SH-SY5Y cells with all-trans-retinoic acid (atRA) generated differentiated neuron-like cells, observed by increased expression of neuronal markers and morphological changes. Exposure of undifferentiated cells to proapoptotic stimuli such as staurosporine, TNF-α, or hypoxia, significantly increased programmed cell death, which was prevented by previous treatment with Epo. In contrast, atRA-differentiated cultures showed cell resistance to apoptosis. No additional effect of Epo was detected in previously differentiated cells. The inhibition of the PI3K/Akt pathway by Ly294002 abrogated the protective effects induced by either Epo or atRA. The effect of atRA was mediated by an increased expression of Bcl-2 whereas the Epo treatment upregulated not only Bcl-2 but also Bcl-xL. This upregulation by Epo was not detected in atRA-differentiated cells, thus confirming the lack of the protective effect of Epo. As expected, assays with AG490, an inhibitor of Jak2, blocked the Epo action only in undifferentiated cells. This reduced neuroprotective function of Epo on SH-SY5Y-differentiated cells could be explained at least in part by downregulation of the Epo receptor expression, which was observed in atRA-differentiated cells. This study shows differential cellular protection induced by Epo at two stages of SH-SY5Y differentiation. The results allow us to suggest that this differential cell behavior can be ascribed to the interaction between atRA and the signaling pathways mediated by Epo. © 2010 Wiley-Liss, Inc.  |l eng 
593 |a Departamento de Química Biológica, Universidad de Buenos Aires, Ciudad Universitaria, Ciudad Autónoma de Buenos Aires C1428EHA, Argentina 
593 |a Consejo Nacional de Investigaciones Científicas Y Técnicas (CONICET), Avda. Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires, Argentina 
690 1 0 |a ALL-TRANS-RETINOIC ACID 
690 1 0 |a APOPTOSIS 
690 1 0 |a DIFFERENTIATION 
690 1 0 |a ERYTHROPOIETIN 
690 1 0 |a ERYTHROPOIETIN RECEPTOR 
690 1 0 |a NEUROPROTECTION 
690 1 0 |a SH-SY5Y CELLS 
690 1 0 |a ERYTHROPOIETIN 
690 1 0 |a ERYTHROPOIETIN RECEPTOR 
690 1 0 |a PHOSPHATIDYLINOSITOL 3 KINASE 
690 1 0 |a PROTEIN BCL 2 
690 1 0 |a PROTEIN BCL XL 
690 1 0 |a PROTEIN KINASE B 
690 1 0 |a RETINOIC ACID 
690 1 0 |a APOPTOSIS 
690 1 0 |a ARTICLE 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a CELL PROTECTION 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DOWN REGULATION 
690 1 0 |a ENZYME INHIBITION 
690 1 0 |a HUMAN 
690 1 0 |a HUMAN CELL 
690 1 0 |a NERVE CELL 
690 1 0 |a NEUROPROTECTION 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a PROTEIN FUNCTION 
690 1 0 |a 1-PHOSPHATIDYLINOSITOL 3-KINASE 
690 1 0 |a APOPTOSIS 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a CELL LINE, TUMOR 
690 1 0 |a CELL SURVIVAL 
690 1 0 |a CYTOPROTECTION 
690 1 0 |a DOWN-REGULATION 
690 1 0 |a ERYTHROPOIETIN, RECOMBINANT 
690 1 0 |a HUMANS 
690 1 0 |a SIGNAL TRANSDUCTION 
690 1 0 |a TRETINOIN 
690 1 0 |a ATRA 
700 1 |a Chamorro, M.E. 
700 1 |a Vota, D.M. 
700 1 |a Callero, M.A. 
700 1 |a Vittori, D.C. 
700 1 |a Nesse, A.B. 
773 0 |d 2010  |g v. 110  |h pp. 151-161  |k n. 1  |p J. Cell. Biochem.  |x 07302312  |t Journal of Cellular Biochemistry 
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