Stat4 is expressed in activated peripheral blood monocytes, dendritic cells, and macrophages at sites of Th1-mediated inflammation

被引:154
作者
Frucht, DM
Aringer, M
Galon, J
Danning, C
Brown, M
Fan, S
Centola, M
Wu, CY
Yamada, N
El Gabalawy, H
O'Shea, JJ
机构
[1] NIAMSD, Lymphocyte Cell Biol Sect, Bethesda, MD 20892 USA
[2] NIAMSD, Clin Res Grp, Bethesda, MD 20892 USA
[3] NIAMSD, Genet Sect, Arthrit & Rheumatism Branch, Bethesda, MD 20892 USA
[4] NCI, Expt Immunol Branch, Bethesda, MD 20892 USA
[5] NCI, Dermatol Branch, Bethesda, MD 20892 USA
[6] NIAID, Clin Invest Lab, Bethesda, MD 20892 USA
关键词
D O I
10.4049/jimmunol.164.9.4659
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Stat4 is a key transcription factor involved in promoting cell-mediated immunity, whose expression in mature cells has been reported to be restricted to T and NK cells. We demonstrate here, however, that Stat4 expression is not restricted to lymphoid cells. In their basal state, monocytes do not express Stat4, Upon activation, however, IFN-gamma- and LPS-treated monocytes and dendritic cells express high levels of Stat4, Monocyte-expressed Stat4 in humans is phosphorylated in response to IFN-alpha, but not IL-12. In contrast, the Th2 cytokines, IL-4 and IL-10, specifically down-regulate Stat4 expression in activated monocytes, while having little effect on Stat6 expression. Moreover, macrophages in synovial tissue obtained from patients with rheumatoid arthritis express Stat4 in vivo, suggesting a potential role in a prototypical Th1-mediated human disease. IFN-alpha -induced Stat4 activation in human monocytes represents a previously unrecognized signaling pathway at sites of Th1 inflammation.
引用
收藏
页码:4659 / 4664
页数:6
相关论文
共 22 条
[1]   INTERLEUKIN-12 (IL-12) INDUCES TYROSINE PHOSPHORYLATION OF JAK2 AND TYK2 - DIFFERENTIAL USE OF JANUS FAMILY TYROSINE KINASES BY IL-2 AND IL-12 [J].
BACON, CM ;
MCVICAR, DW ;
ORTALDO, JR ;
REES, RC ;
O'SHEA, JJ ;
JOHNSTON, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) :399-404
[2]   INTERLEUKIN-12 INDUCES TYROSINE PHOSPHORYLATION AND ACTIVATION OF STAT4 IN HUMAN-LYMPHOCYTES [J].
BACON, CM ;
PETRICOIN, EF ;
ORTALDO, JR ;
REES, RC ;
LARNER, AC ;
JOHNSTON, JA ;
O'SHEA, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7307-7311
[3]   The neglected role of type I interferon in the T-cell response: Implications for its clinical use [J].
Belardelli, F ;
Gresser, I .
IMMUNOLOGY TODAY, 1996, 17 (08) :369-372
[4]   Cellular responses to interferon-gamma [J].
Boehm, U ;
Klamp, T ;
Groot, M ;
Howard, JC .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :749-795
[5]   RHEUMATOID ARTHRITIS-LIKE DISEASE AFTER ALPHA-INTERFERON THERAPY [J].
CHAZERAIN, P ;
MEYER, O ;
KAHN, MF .
ANNALS OF INTERNAL MEDICINE, 1992, 116 (05) :427-427
[6]  
Cho SS, 1996, J IMMUNOL, V157, P4781
[7]   STATs and gene regulation [J].
Darnell, JE .
SCIENCE, 1997, 277 (5332) :1630-1635
[8]  
GORDON S, 1999, FUNDAMENTAL IMMUNOLO, P533
[9]   IL-12 acts directly on DC to promote nuclear localization of NF-κB and primes DC for IL-12 production [J].
Grohmann, U ;
Belladonna, ML ;
Bianchi, R ;
Orabona, C ;
Ayroldi, E ;
Fioretti, MC ;
Puccetti, P .
IMMUNITY, 1998, 9 (03) :315-323
[10]   STATs: Signal transducers and activators of transcription [J].
Ihle, JN .
CELL, 1996, 84 (03) :331-334