Complex modulation of cell type-specific signaling in response to type I Interferons

被引:412
作者
van Boxel-Dezaire, Anette H. H. [1 ]
Rani, M. R. Sandhya [1 ]
Stark, George R. [1 ]
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Mol Genet, Cleveland, OH 44195 USA
关键词
D O I
10.1016/j.immuni.2006.08.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The type I interferons (IFNs) are plelotropic cytokines that regulate many different cellular functions. The major signaling pathway activated by type I IFNs involves sequential phosphorylation of the tyrosine residues of the Janus kinase (JAK) and signal transducers and activators of transcription (STAT) proteins, providing the primary mechanism through which gene expression is induced. Recent work has shown that the responses are quite complex, as shown by different responses to specific subtypes of type I IFN, activation of kinases in addition to JAKs, patterns of activation of all seven STATs in different cells, and activation of transcription factors other than STATs. The type I IFNs use this complexity to regulate many different biological functions in different types of cells, by activating different specific signals and patterns of gene expression.
引用
收藏
页码:361 / 372
页数:12
相关论文
共 123 条
[71]   IFN-stimulated gene 15 is synergistically activated through interactions between the myelocyte/lymphocyte-specific transcription factors, PU.1, IFN regulatory factor-8/IFN consensus sequence binding protein, and IFN regulatory factor-4: Characterization of a new subtype of IFN-stimulated response element [J].
Meraro, D ;
Gleit-Kielmanowicz, M ;
Hauser, H ;
Levi, BZ .
JOURNAL OF IMMUNOLOGY, 2002, 168 (12) :6224-6231
[72]   The production of IL-1 receptor antagonist in IFN-β-stimulated human monocytes depends on the activation of phosphatidylinositol 3-kinase but not of STAT1 [J].
Molnarfi, N ;
Hyka-Nouspikel, N ;
Gruaz, L ;
Dayer, JM ;
Burger, D .
JOURNAL OF IMMUNOLOGY, 2005, 174 (05) :2974-2980
[73]   A PI-3 kinase-dependent, Stat1-independent signaling pathway regulates interferon-stimulated monocyte adhesion [J].
Navarro, A ;
Anand-Apte, B ;
Tanabe, Y ;
Feldman, G ;
Larner, AC .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (04) :540-545
[74]   Coordinated and distinct roles for IFN-αβ, IL-12, and IL-15 regulation of NK cell responses to viral infection [J].
Nguyen, KB ;
Salazar-Mather, TP ;
Dalod, MY ;
Van Deusen, JB ;
Wei, XQ ;
Liew, FY ;
Caligiuri, MA ;
Durbin, JE ;
Biron, CA .
JOURNAL OF IMMUNOLOGY, 2002, 169 (08) :4279-4287
[75]   THE HUMAN INTERFERON-ALPHA/BETA RECEPTOR - CHARACTERIZATION AND MOLECULAR-CLONING [J].
NOVICK, D ;
COHEN, B ;
RUBINSTEIN, M .
CELL, 1994, 77 (03) :391-400
[76]   DIFFERENT INTERACTIONS OF INTERFERON-ALPHA SUBTYPES AT THE SURFACE OF EPITHELIAL AND LYMPHOID-CELLS [J].
OVERALL, ML ;
CHAMBERS, P ;
HERTZOG, PJ .
JOURNAL OF INTERFERON RESEARCH, 1992, 12 (04) :281-288
[77]   USE OF A SELECTABLE MARKER REGULATED BY ALPHA INTERFERON TO OBTAIN MUTATIONS IN THE SIGNALING PATHWAY [J].
PELLEGRINI, S ;
JOHN, J ;
SHEARER, M ;
KERR, IM ;
STARK, GR .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4605-4612
[78]   Interferons, interferon-like cytokines, and their receptors [J].
Pestka, S ;
Krause, CD ;
Walter, MR .
IMMUNOLOGICAL REVIEWS, 2004, 202 :8-32
[79]   STAT3 as an adapter to couple phosphatidylinositol 3-kinase to the IFNAR1 chain of the type I interferon receptor [J].
Pfeffer, LM ;
Mullersman, JE ;
Pfeffer, SR ;
Murti, A ;
Shi, W ;
Yang, CH .
SCIENCE, 1997, 276 (5317) :1418-1420
[80]   Mechanisms of type-I- and type-II-interferon-mediated signalling [J].
Platanias, LC .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (05) :375-386