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This version published online on May 13, 2004
Molecular Endocrinology, doi:10.1210/me.2004-0098
A more recent version of this article appeared on August 1, 2004
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Submitted on March 9, 2004
Accepted on May 3, 2004

17{beta}-Estradiol Inhibits Class II MHC Expression: Influence on Histone Modifications and CBP Recruitment to the Class II MHC Promoter

Jill Adamski, Zhendong Ma, Susan Nozell, and Etty N. Benveniste*

Department of Cell Biology, University of Alabama at Birmingham, Birmingham, AL 35294

* To whom correspondence should be addressed. E-mail: tika{at}uab.edu.

Major histocompatibility complex (MHC) class II proteins are important for the initiation of immune responses and are essential for specific recognition of foreign antigens by the immune system. Regulation of class II MHC expression primarily occurs at the transcriptional level. The class II transactivator (CIITA) protein is the master regulator that is essential for both constitutive and interferon-{gamma} (IFN-{gamma}) inducible class II MHC expression. Estrogen (17{beta}-E2) has been shown to have immunomodulatory effects. In this study, we show that 17{beta}-E2 downregulates IFN-{gamma} inducible class II MHC protein levels on brain endothelial cells, as well as other cell types (astrocytes, fibrosacroma cells, macrophages). The inhibitory effects of 17{beta}-E2 on class II MHC expression are not due to changes in CIITA mRNA or protein levels, rather, 17{beta}-E2 mediates inhibition at the level of class II MHC gene expression. We demonstrate that 17{beta}-E2 attenuates H3 and H4 histone acetylation and CREB-binding protein (CBP) association with the class II MHC promoter, suggesting that 17{beta}-E2 inhibits class II MHC expression by a novel mechanism involving modification of the histone acetylation status of the class II MHC promoter.


Key words: estrogen • class II MHC • CIITA • CBP • autoimmunity

NURSA Molecule Pages Link:

Ligands:   17β-Estradiol



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