In vitro addition of stem cell factor (SCF) to c-kit-expressing A(1)-A(4) spermatogonia from prepuberal mice stimulates their progression into the mitotic cell cycle and significantly reduces apoptosis in these cells. SCF addition results in a transient activation of extracellular signal-regulated kinases (Erk)1/2 as well as of phosphatidylinositol 3-kinase (PI3K)-dependent Akt kinase. These events are followed by a rapid re-distribution of cyclin D3, which becomes predominantly nuclear, whereas its total cellular amount does not change. Nuclear accumulation of cyclin D3 is coupled to transient activation of the associated kinase activity, assayed using the retinoblastoma protein (Rb) as a substrate. These events were followed by a transient accumulation of cyclin E, stimulation of the associated histone H1-kinase activity, a delayed accumulation of cyclin A2, and Rb hyper-phosphorylation. All the events associated with SCF-induced cell cycle progression are inhibited by the addition of either a PI3K inhibitor or a mitogen-activated protein-kinase kinase (MEK) inhibitor, indicating that both MEK and PI3K are essential for c-kit-mediated proliferative response. On the contrary, the anti-apoptotic effect of SCF is not influenced by the separate addition of either MEK or PI3K inhibitors. Thus, SCF effects on mitogenesis and survival in c-kit expressing spermatogonia rely on different signal transduction pathways.

DOLCI IANNINI, S., Pellegrini, M., Di Agostino, S., Geremia, R., Rossi, P. (2001). Signaling through extracellular signal-regulated kinase is required for spermatogonial proliferative response to stem cell factor. THE JOURNAL OF BIOLOGICAL CHEMISTRY, 276(43), 40225-40233 [10.1074/jbc.M105143200].

Signaling through extracellular signal-regulated kinase is required for spermatogonial proliferative response to stem cell factor

DOLCI IANNINI, SUSANNA;GEREMIA, RAFFAELE;ROSSI, PELLEGRINO
2001-10-26

Abstract

In vitro addition of stem cell factor (SCF) to c-kit-expressing A(1)-A(4) spermatogonia from prepuberal mice stimulates their progression into the mitotic cell cycle and significantly reduces apoptosis in these cells. SCF addition results in a transient activation of extracellular signal-regulated kinases (Erk)1/2 as well as of phosphatidylinositol 3-kinase (PI3K)-dependent Akt kinase. These events are followed by a rapid re-distribution of cyclin D3, which becomes predominantly nuclear, whereas its total cellular amount does not change. Nuclear accumulation of cyclin D3 is coupled to transient activation of the associated kinase activity, assayed using the retinoblastoma protein (Rb) as a substrate. These events were followed by a transient accumulation of cyclin E, stimulation of the associated histone H1-kinase activity, a delayed accumulation of cyclin A2, and Rb hyper-phosphorylation. All the events associated with SCF-induced cell cycle progression are inhibited by the addition of either a PI3K inhibitor or a mitogen-activated protein-kinase kinase (MEK) inhibitor, indicating that both MEK and PI3K are essential for c-kit-mediated proliferative response. On the contrary, the anti-apoptotic effect of SCF is not influenced by the separate addition of either MEK or PI3K inhibitors. Thus, SCF effects on mitogenesis and survival in c-kit expressing spermatogonia rely on different signal transduction pathways.
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/16
English
Con Impact Factor ISI
Animals; Apoptosis; Proto-Oncogene Proteins c-kit; S Phase; Cyclin D3; Mice; Stem Cell Factor; Phosphatidylinositol 3-Kinases; Cyclin A; Cells, Cultured; Mitogens; Mitogen-Activated Protein Kinase 3; Mitogen-Activated Protein Kinases; G1 Phase; Mitogen-Activated Protein Kinase 1; DNA Fragmentation; Signal Transduction; Mitogen-Activated Protein Kinase Kinases; Male; Spermatogonia; Protein Transport; Cell Division; Cyclins
DOLCI IANNINI, S., Pellegrini, M., Di Agostino, S., Geremia, R., Rossi, P. (2001). Signaling through extracellular signal-regulated kinase is required for spermatogonial proliferative response to stem cell factor. THE JOURNAL OF BIOLOGICAL CHEMISTRY, 276(43), 40225-40233 [10.1074/jbc.M105143200].
DOLCI IANNINI, S; Pellegrini, M; Di Agostino, S; Geremia, R; Rossi, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/65815
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