Prostaglandins, mainly those of the E series (PGE), are modulators of immune responses. Indeed PGE(2) inhibits T cell activation and the transcription of the interleukin-2 (IL-2) gene, the major T cell growth factor, We observed that PGE(2) inhibits IL-2 promoter transcription activity by interfering with signals activating the (-96 to -66 bp) octamer motif. This motif binds Oct-1 and Oct-2 as well as the phorbol ester and calcium ionophore-inducible jun and fos AP-1 factors. The PGE(2)-dependent down-modulation is observed in the presence of either the endogenous transacting factor Oct-1 or the exogenously expressed Oct-2. PGE(2) does not regulate octamer function by influencing the jun and fos mRNA or Oct-1 protein levels or their DNA-binding abilities. Functional dissection of the octamer motif, through mutations of either the AP-1 or the octamer sites, revealed that the AP-1 site is dispensable for PGE(2)-dependent inhibition which instead may occur through the interference with the Oct-mediated transactivation of the octamer element, Our data suggest that the Oct-octamer interaction is a novel target of the PGE(2)-induced down-regulation of the IL-2 promoter, (C) 1996 Academic Press, Inc.
Prostaglandin E2 inhibits the interleukin-2 promoter activity through down-regulation of the oct-dependent transcription of the octamer motif / Felli, MARIA PIA; Moschella, C.; Farina, A. R.; Alesse, E.; Screpanti, Isabella; Teti, D.; Frati, Luigi; Gulino, Alberto. - In: CELLULAR IMMUNOLOGY. - ISSN 0008-8749. - STAMPA. - 172(2):(1996), pp. 229-234. [10.1006/cimm.1996.0237]
Prostaglandin E2 inhibits the interleukin-2 promoter activity through down-regulation of the oct-dependent transcription of the octamer motif.
FELLI, MARIA PIA;SCREPANTI, Isabella;FRATI, Luigi;GULINO, Alberto
1996
Abstract
Prostaglandins, mainly those of the E series (PGE), are modulators of immune responses. Indeed PGE(2) inhibits T cell activation and the transcription of the interleukin-2 (IL-2) gene, the major T cell growth factor, We observed that PGE(2) inhibits IL-2 promoter transcription activity by interfering with signals activating the (-96 to -66 bp) octamer motif. This motif binds Oct-1 and Oct-2 as well as the phorbol ester and calcium ionophore-inducible jun and fos AP-1 factors. The PGE(2)-dependent down-modulation is observed in the presence of either the endogenous transacting factor Oct-1 or the exogenously expressed Oct-2. PGE(2) does not regulate octamer function by influencing the jun and fos mRNA or Oct-1 protein levels or their DNA-binding abilities. Functional dissection of the octamer motif, through mutations of either the AP-1 or the octamer sites, revealed that the AP-1 site is dispensable for PGE(2)-dependent inhibition which instead may occur through the interference with the Oct-mediated transactivation of the octamer element, Our data suggest that the Oct-octamer interaction is a novel target of the PGE(2)-induced down-regulation of the IL-2 promoter, (C) 1996 Academic Press, Inc.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.