The time-course of cyclic AMP signaling is critical for leukemia U-937 cell differentiation

The regulation of the cAMP signaling is intimately involved in several cellular processes, including cell differentiation. Here, we provide strong evidence supporting that the time-course of cAMP signal is critical for leukemia U-937 cell differentiation. Three stimulating-cAMP agents were used to a...

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Autor principal: Shayo, C.
Otros Autores: Legnazzi, B.L, Monczor, F., Fernández, N., Riveiro, M.E, Baldi, A., Davio, C.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Academic Press Inc. 2004
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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100 1 |a Shayo, C. 
245 1 4 |a The time-course of cyclic AMP signaling is critical for leukemia U-937 cell differentiation 
260 |b Academic Press Inc.  |c 2004 
270 1 0 |m Shayo, C.; Inst. de Biol. y Med. Experimental, Buenos Aires, Argentina; email: cshayo@dna.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a The regulation of the cAMP signaling is intimately involved in several cellular processes, including cell differentiation. Here, we provide strong evidence supporting that the time-course of cAMP signal is critical for leukemia U-937 cell differentiation. Three stimulating-cAMP agents were used to analyze the correlation between cAMP time-course and cell differentiation. All three agents denoted similar cAMP maximal responses in dose-response experiments. The kinetic of desensitization showed differential characteristics, while H2 receptor desensitized homologously without affecting PGE2 or forskolin effect, PGE2 response showed mixed desensitization characterized by a homologous initial phase followed by a heterologous phase. Regarding forskolin, long-term stimuli attenuated PGE2 and H2 agonist response without affecting adenylyl cyclase activity. In the absence of phosphodiesterase inhibitors, the three agents induced similar maximal cAMP levels after 5min, but only that induced by the H2 agonist returned to basal levels. Consistent with this observation, H2 agonist was not able to induce U-937 cell maturation in contrast to PGE2 and forskolin, supporting the importance of time-course signaling in the determination of cell behavior. © 2003 Elsevier Inc. All rights reserved.  |l eng 
593 |a Inst. de Biol. y Med. Experimental, Buenos Aires, Argentina 
593 |a Laboratorio de Radioisótopos, Fac. de Farmacia y Bioquímica, Universidad de Buenos Aires, Argentina 
593 |a Depto. Fisiol., Biol. Molec. y Cel., Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina 
593 |a Consejo Nac. de Invest. Cie. y Tec., Buenos Aires, Argentina 
690 1 0 |a CAMP SIGNALING 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a LEUKEMIA 
690 1 0 |a AMTHAMINE 
690 1 0 |a CALCIUM 
690 1 0 |a COMPLEMENT COMPONENT C5A 
690 1 0 |a CYCLIC AMP 
690 1 0 |a FORSKOLIN 
690 1 0 |a HISTAMINE AGONIST 
690 1 0 |a HISTAMINE H2 RECEPTOR 
690 1 0 |a MYC PROTEIN 
690 1 0 |a PROSTAGLANDIN E RECEPTOR 
690 1 0 |a PROSTAGLANDIN E2 
690 1 0 |a PROSTAGLANDIN RECEPTOR STIMULATING AGENT 
690 1 0 |a PROTEIN C FOS 
690 1 0 |a RECOMBINANT PROTEIN 
690 1 0 |a THIAZOLE DERIVATIVE 
690 1 0 |a ARTICLE 
690 1 0 |a BIOSYNTHESIS 
690 1 0 |a CELL DIFFERENTIATION 
690 1 0 |a CELL DIVISION 
690 1 0 |a CELL MATURATION 
690 1 0 |a CELL STRAIN U937 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CORRELATION ANALYSIS 
690 1 0 |a DESENSITIZATION 
690 1 0 |a DOSE RESPONSE 
690 1 0 |a DRUG EFFECT 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a GENETICS 
690 1 0 |a HUMAN 
690 1 0 |a HUMAN CELL 
690 1 0 |a KINETICS 
690 1 0 |a LEUKEMIA CELL 
690 1 0 |a METABOLISM 
690 1 0 |a PHYSIOLOGY 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a SEQUENCE HOMOLOGY 
690 1 0 |a SIGNAL TRANSDUCTION 
690 1 0 |a TIME 
700 1 |a Legnazzi, B.L. 
700 1 |a Monczor, F. 
700 1 |a Fernández, N. 
700 1 |a Riveiro, M.E. 
700 1 |a Baldi, A. 
700 1 |a Davio, C. 
773 0 |d Academic Press Inc., 2004  |g v. 314  |h pp. 798-804  |k n. 3  |p Biochem. Biophys. Res. Commun.  |x 0006291X  |w (AR-BaUEN)CENRE-905  |t Biochemical and Biophysical Research Communications 
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