Prosaposin treatment induces PC12 entry in the S phase of the cell cycle and prevents apoptosis: activation of ERKs and sphingosine kinase
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- ROBERTA MISASI
- Dipartimento di Medicina Sperimentale e Patologia Università ‘La Sapienza’ Roma Rome Italy
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- MAURIZIO SORICE
- Dipartimento di Medicina Sperimentale e Patologia Università ‘La Sapienza’ Roma Rome Italy
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- LUISA DI MARZIO
- Dipartimento di Medicina Sperimentale Università di L’Aquila Italy
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- W. MARIE CAMPANA
- Department of Neurosciences University of California San Diego School of Medicine Center for Molecular Genetics LaJolla California USA
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- SABRINA MOLINARI
- Dipartimento di Medicina Sperimentale e Patologia Università ‘La Sapienza’ Roma Rome Italy
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- MARIA GRAZIA CIFONE
- Dipartimento di Medicina Sperimentale Università di L’Aquila Italy
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- ANTONIO PAVAN
- Dipartimento di Medicina Sperimentale Università di L’Aquila Italy
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- GIUSEPPE M. PONTIERI
- Dipartimento di Medicina Sperimentale e Patologia Università ‘La Sapienza’ Roma Rome Italy
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- JOHN S. O’BRIEN
- Department of Neurosciences University of California San Diego School of Medicine Center for Molecular Genetics LaJolla California USA
抄録
<jats:title>ABSTRACT</jats:title><jats:p>We report that prosaposin treatment induced extracellular signal‐regulated kinases (ERKs) and sphingosine kinase activity, increased DNA synthesis, and prevented cell apoptosis. Prosaposin treatment induced pheochromocytoma cells (PC12) to enter the S phase of the cell cycle;this effect was inhibited by the MEK inhibitor PD98059, indicating that prosaposin‐induced ERK phosphorylation is required for stimulation of DNA synthesis. The prosaposin effect was also inhibited by pertussis toxin, indicating that the prosaposin receptor is a G‐protein‐coupled receptor. Prosaposin rescued PC12 cells from apoptosis induced by staurosporine or ceramide. Sphingosine kinase activity was increased by prosaposin treatment. We propose that this effect is a mechanism underlying the proliferative and anti‐apoptotic functions of prosaposin. Prosaposin appears to be a key regulatory factor in the ceramide‐S‐1‐P rheostat, which regulates cell fate.—Misasi, R., Sorice, M., Di Marzio, L., Campana, W. M., Molinari, S., Cifone, M. G., Pavan, A., Pontieri, G. M., O'Brien, J. S. Prosaposin treatment induces PC12 entry in the S phase of the cell cycle and prevents apoptosis: activation of ERKs and sphingosine kinase. <jats:italic>FASEB J.</jats:italic> 15, 467‐474 (2001)</jats:p>
収録刊行物
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- The FASEB Journal
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The FASEB Journal 15 (2), 467-474, 2001-02
Wiley
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詳細情報 詳細情報について
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- CRID
- 1364233270688145792
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- NII論文ID
- 30018584253
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- ISSN
- 15306860
- 08926638
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