Transkriptionelle Regulation des humanen Interferon-gamma-Promotors in T-Lymphocyten


Autoria(s): Barbulescu, Karina
Data(s)

2000

Resumo

Interferon-gamma is mainly produced by activated T helper cells and cytotoxic T lymphocytes and sustains the immune-defense against viral and bacterial infections. For a better understanding of IFN-gamma promoter regulation in T cells, different DNA-binding motivs were examined. Hereby, a new motiv (-196 to -183) was identified, that binds to the transcription factor AP-1 in T helper cells and Jurkat T cells. This factor acts as an essential activator protein. Further investigation demonstrated that IL-12 and IL-18 induce different regulatory pathways. Both AP-1 and STAT-4 bindings at their cognate DNA elements (-196 to -183 and -224 to -215) are required for the IL-12 dependent activation whereas IL-18 causes direct activation via AP-1.Moreover, the TH2 cytokine IL-4 represses significantly the IFN-gamma promoter activity in CD4+ T cells. IL-4 induces GATA-3, that interacts with two DNA-motivs (-111 to -87) at the IFN-gamma promoter.Furthermore, transgenic mice were generated, yielding a human IFN-gamma promoter construct (410 bp) under the control of a luciferase reporter gene. The data demonstrated a specific IFN-gamma promoter activation by antiCD3 plus antiCD28 in CD4+ and CD8+ T cells. The luciferase activty in CD4+ T cells was reinforced by addition of IL-12 and IL-18 and repressed by IL-4.

Formato

application/pdf

Identificador

urn:nbn:de:hebis:77-353

http://ubm.opus.hbz-nrw.de/volltexte/2000/35/

Idioma(s)

ger

Publicador

Universität Mainz

10: Biologie. 10: Biologie

Direitos

http://ubm.opus.hbz-nrw.de/doku/urheberrecht.php

Palavras-Chave #Life sciences
Tipo

Thesis.Doctoral