HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Request Permissions Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Samten, B. Articles by Barnes, P. F. Search for Related Content PubMed PubMed Citation Articles by Samten, B. Articles by Barnes, P. F.

Cyclic AMP Response Element-Binding Protein Positively Regulates Production of IFN- by T Cells in Response to a Microbial Pathogen ¹

Buka Samten^*,, Susan T. Howard^*,, Steven E. Weis, Shiping Wu^*,, Homayoun Shams^*,, James C. Townsend^*, Hassan Safi^*, and Peter F. Barnes^2,,

^* Center for Pulmonary and Infectious Disease Control, Departments of Microbiology and Immunology and Medicine, University of Texas Health Center, Tyler, TX 75708; and Department of Internal Medicine, University of North Texas Health Sciences Center, Fort Worth, TX 76107

IFN- is essential for resistance to many intracellular pathogens, including Mycobacterium tuberculosis. Transcription of the IFN- gene in activated T cells is controlled by the proximal promoter element (–73 to –48 bp). CREB binds to the IFN- proximal promoter, and binding is enhanced by phosphorylation of CREB. Studies in human T cell lines and in transgenic mice have yielded conflicting results about whether CREB is a positive or a negative regulator of IFN- transcription. To determine the role of CREB in mediating IFN- production in response to a microbial pathogen, we evaluated the peripheral blood T cell response to M. tuberculosis in healthy tuberculin reactors. EMSAs, chromatin immunoprecipitation, and Western blotting demonstrated that stimulation of PBMC with M. tuberculosis induced phosphorylation and enhanced binding of CREB to the IFN- proximal promoter. Neutralization of CREB with intracellular Abs or down-regulation of CREB levels with small interfering RNA decreased M. tuberculosis-induced production of IFN- and IFN- mRNA expression. In addition, M. tuberculosis-stimulated T cells from tuberculosis patients, who have ineffective immunity, showed diminished IFN- production, reduced amounts of CREB binding to the IFN- proximal promoter, and absence of phosphorylated CREB. These findings demonstrate that CREB positively regulates IFN- production by human T cells that respond to M. tuberculosis.

This article has been cited by other articles:

				X. Wang, P. F. Barnes, K. M. Dobos-Elder, J. C. Townsend, Y.-t. Chung, H. Shams, S. E. Weis, and B. Samten ESAT-6 Inhibits Production of IFN-{gamma} by Mycobacterium tuberculosis-Responsive Human T Cells J. Immunol., March 15, 2009; 182(6): 3668 - 3677. [Abstract] [Full Text] [PDF]

				B. Samten, J. C. Townsend, S. E. Weis, A. Bhoumik, P. Klucar, H. Shams, and P. F. Barnes CREB, ATF, and AP-1 Transcription Factors Regulate IFN-{gamma} Secretion by Human T Cells in Response to Mycobacterial Antigen J. Immunol., August 1, 2008; 181(3): 2056 - 2064. [Abstract] [Full Text] [PDF]