SharePoint
Aide
Faire avancer la sûreté nucléaire

La Recherchev2

Publications

Promoter sequences involved in transforming growth factor beta 1 gene induction in HaCaT keratinocytes after gamma irradiation


Fermer

Authentification

Email :

Mot de passe :

Gault, N; Vozenin-Brotons, MC; Calenda, A; Lefaix, JL; Martin, MT Radiation Research, Mar 2002 , 157: (3) 249-255

Type de document > *Article de revue

Mots clés > cytokine, irradiation, syndrome cutané

Unité de recherche > UPRES (Radiosensibilité des Tumeurs et Tissus Sains)

Auteurs > VOZENIN-BROTONS Marie Catherine

Date de publication > 01/03/2002

Résumé

Transforming growth factor beta 1 (TGFB1) is a cytokine involved in the development of both acute and late cutaneous radiation syndromes. We previously demonstrated that ionizing radiation induces TGFB1 expression in vivo in pig skin within a few hours. The purpose of the present study was to develop an in vitro human model to identify the mechanisms of this early activation. Accordingly, human HaCaT keratinocytes were irradiated with a single dose of 20 Gy. First, radiation-induced TGFB1 overexpression was checked at both the transcriptional and transductional levels in HaCaT cells. Then electrophoretic mobility shift assays (EMSA) and transient transfection with various TGFB1 promoter constructs were used to identify the sequences involved in regulating this promoter. ENISA analysis showed the induction of nuclear protein binding activity by T irradiation to the -365 AP1 sequence (TGTCTCA), suggesting the involvement of AP1 sequences in the regulation of TGFBI transcription. In gene reporter assays, maximal TGFBI promoter activation was found for the longest construct, which contains two AP1 sequences. However, assays with constructs including deletions showed that these two AP1 sequences were not sufficient to confer TGFBI inducibility. These results showed for the first time, to our knowledge, that transcriptional regulation is involved in radiation-induced activation of TGFB1 gene expression.