In the skin, the generation of intracellular ceramide may provide a link between an extracellular signal and the induction of apoptosis for the elimination of damaged cells. Previous sturdies have shown that cell permeant ceramide are involved in signal transduction, cell cycle regulation and apoptosis in different cell types. The aim of the present study was to investigate the intracellular apoptotic signal induced by permeant ceramides on cultured normal human keratinocytes (NHK). NHK from neonatal skin were cultured in serum free medium with or without ceramide 2 (CER-2, n-acetil-sphingosine) 20 M, 40 M. Cell cycle was investigated by FACS analysis, and western blot analysis of cyclin D1 and Rb dephosphorilation. Apoptosis was studied by TUNEL staining and western blot analysis of BCL-2 protein, p53 and p21. FACS analysis demonstrated a G1 arrest 48 h after ceramide addition, accompanied by down regulation of cyclin D1 and by Kb dephosphorilation. TUNEL staining showed the presence of CER-2-induced apoptosis after 48, 72 and 96 h of culture. Western blot analysis demonstrated that CER-2 induces a down regulation of BCL-2 after 24 h up to 96 h, and an up regulation of p53 after 24 h. No modifications were noted in p21 levels. These results demonstrate that in NHK CER-2 cell permeant ceramide induces cell cycle arrest in G1, which precedes apoptosis.
|Data di pubblicazione:||1999|
|Titolo:||Ceramide 2(N-acetyl sphingosine) induces G1 arrest and Rb dephosphorilation in cultured human keratinocytes|
|Autori:||Di Nardo A; Magnoni C; Benassi L; Bertazzoni G; Seidenari S; Giannetti A|
|Nome del convegno:||ESDR Annual Meeting 1999 – European Society for Investigative Dermatology|
|Luogo del convegno:||Montpellier|
|Data del convegno:||22-25 september|
|Appare nelle tipologie:||Abstract in Rivista|
File in questo prodotto:
I documenti presenti in Iris Unimore sono rilasciati con licenza Creative Commons Attribuzione - Non commerciale - Non opere derivate 3.0 Italia, salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris