We investigated the subcellular localization of PDE5 in in vitro human myometrial cells. We demonstrated for the first time that PDE5 is localized in discrete cytoplasmic foci and vesicular compartments corresponding to centrosomes. We also found that PDE5 intracellular localization is not cell- or species-specific, as it is conserved in different animal and human cells. PDE5 protein levels are strongly regulated by the mitotic activity of the smooth muscle cells (SMCs), as they were increased in quiescent, contractile myometrial cultures, and conditions in which proliferation was inhibited. In contrast, PDE1C levels decreased in all conditions that inhibited proliferation. This mirrored the enzymatic activity of both PDE5 and PDE1C. Increasing cGMP intracellular levels by dbcGMP or sildenafil treatments did not block proliferation, while dbcAMP inhibited myometrial cell proliferation. Together, these results suggest that PDE5 regulation of cGMP intracellular levels is not involved in the control of SMC cycle progression, but may represent one of the markers of the contractile phenotype.

DOLCI IANNINI, S., Belmonte, A., Santone, R., Giorgi, M., Pellegrini, M., Carosa, E., et al. (2006). Subcellular localization and regulation of type-1C and type-5 phosphodiesterases. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 341(3), 837-846 [10.1016/j.bbrc.2006.01.035].

Subcellular localization and regulation of type-1C and type-5 phosphodiesterases

DOLCI IANNINI, SUSANNA;PICCIONE, EMILIO;JANNINI, EMMANUELE ANGELO FRANCESCO
2006-03-17

Abstract

We investigated the subcellular localization of PDE5 in in vitro human myometrial cells. We demonstrated for the first time that PDE5 is localized in discrete cytoplasmic foci and vesicular compartments corresponding to centrosomes. We also found that PDE5 intracellular localization is not cell- or species-specific, as it is conserved in different animal and human cells. PDE5 protein levels are strongly regulated by the mitotic activity of the smooth muscle cells (SMCs), as they were increased in quiescent, contractile myometrial cultures, and conditions in which proliferation was inhibited. In contrast, PDE1C levels decreased in all conditions that inhibited proliferation. This mirrored the enzymatic activity of both PDE5 and PDE1C. Increasing cGMP intracellular levels by dbcGMP or sildenafil treatments did not block proliferation, while dbcAMP inhibited myometrial cell proliferation. Together, these results suggest that PDE5 regulation of cGMP intracellular levels is not involved in the control of SMC cycle progression, but may represent one of the markers of the contractile phenotype.
17-mar-2006
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore BIO/16 - ANATOMIA UMANA
English
Con Impact Factor ISI
Humans; 3',5'-Cyclic-GMP Phosphodiesterases; MAP Kinase Kinase 1; Cyclic Nucleotide Phosphodiesterases, Type 1; Cell Proliferation; Protein Kinase Inhibitors; Cyclic Nucleotide Phosphodiesterases, Type 5; Culture Media, Serum-Free; Cyclic GMP; Phosphoric Diester Hydrolases; MAP Kinase Signaling System; Gene Expression Regulation, Enzymologic; Cells, Cultured; Adult; Up-Regulation; Myometrium; Female; Protein Transport
DOLCI IANNINI, S., Belmonte, A., Santone, R., Giorgi, M., Pellegrini, M., Carosa, E., et al. (2006). Subcellular localization and regulation of type-1C and type-5 phosphodiesterases. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 341(3), 837-846 [10.1016/j.bbrc.2006.01.035].
DOLCI IANNINI, S; Belmonte, A; Santone, R; Giorgi, M; Pellegrini, M; Carosa, E; Piccione, E; Lenzi, A; Jannini, Eaf
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/25754
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