Negative regulation of interferon-γ/STAT1 signaling through cell adhesion and cell density-dependent STAT1 dephosphorylation

被引:6
作者
Chen, Zhimin [1 ]
Ma, Xiuquan [2 ]
Zhang, Haohao [1 ]
Sun, Xiaoxiao [1 ]
Shen, Shensi [1 ]
Li, Ying [2 ]
Gu, Yuan [1 ]
Wang, Ying [1 ]
Yan, Shoushen [1 ]
Yu, Qiang [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 201203, Peoples R China
关键词
STAT; Interferon-gamma; T-cell protein tyrosine phosphatase; Extracellular matrix; Actin cytoskeleton; Tyrosine dephosphorylation; PROTEIN-TYROSINE-PHOSPHATASE; INTERFERON-GAMMA RECEPTOR; APOPTOSIS-INDUCING LIGAND; MHC CLASS-I; IFN-GAMMA; INHIBITORY FACTOR; TUMOR-METASTASIS; T-CELLS; GROWTH; ACTIVATION;
D O I
10.1016/j.cellsig.2011.04.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Signal transducer and activator of transcription 1 (STAT1) is an important mediator for cytokine signal transduction, particularly IFN-gamma. Following IFN-gamma stimulation, STAT1 is activated through tyrosine phosphorylation. Little is known about the function and regulation of STAT1 dephosphorylation after activation. We studied the regulation and function of STAT1 dephosphorylation in different types of cells and found that the phosphorylated STAT1 was quickly dephosphorylated in most of epithelial cells. Further studies revealed that the dephosphorylation of STAT1 was regulated by cell shape/adhesion. Actin cytoskeleton and extracellular matrix (ECM) proteins mediated the STAT1 dephosphorylation through the T-cell protein tyrosine phosphatase TCPTP. Inactivation of the dephosphorylation system by cell detachment rendered the cells more sensitive to IFN-gamma-induced cell death. Our results revealed a novel mechanism in regulating IFN-gamma/STAT1 signaling. This cell adhesion and cell cytoskeleton-dependent STAT1 dephosphorylation system may have a role in IFN-gamma-mediated immunosurveillance for cancer cells by inducing anoikis of detached metastatic cancer cells. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1404 / 1412
页数:9
相关论文
共 56 条
[1]   The IFN gamma receptor: A paradigm for cytokine receptor signaling [J].
Bach, EA ;
Aguet, M ;
Schreiber, RD .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :563-&
[2]  
Bach EA, 1996, MOL CELL BIOL, V16, P3214
[3]  
BRUNDA MJ, 1994, J LEUKOCYTE BIOL, V55, P280
[4]   Cell growth arrest and induction of cyclin-dependent kinase inhibitor p21(WAF1/CIP1) mediated by STAT1 [J].
Chin, YE ;
Kitagawa, M ;
Su, WCS ;
You, ZH ;
Iwamoto, Y ;
Fu, XY .
SCIENCE, 1996, 272 (5262) :719-722
[5]   Interferon-inducible T cell alpha chemoattractant (I-TAC): A novel non-ELR CXC chemokine with potent activity on activated T cells through selective high affinity binding to CXCR3 [J].
Cole, KE ;
Strick, CA ;
Paradis, TJ ;
Ogborne, KT ;
Loetscher, M ;
Gladue, RP ;
Lin, W ;
Boyd, JG ;
Moser, B ;
Wood, DE ;
Sahagan, BG ;
Neote, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (12) :2009-2021
[6]   JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS [J].
DARNELL, JE ;
KERR, IM ;
STARK, GR .
SCIENCE, 1994, 264 (5164) :1415-1421
[7]   Interferon γ inhibits growth of human pancreatic carcinoma cells via caspase-1 dependent induction of apoptosis [J].
Detjen, KM ;
Farwig, K ;
Welzel, M ;
Wiedenmann, B ;
Rosewicz, S .
GUT, 2001, 49 (02) :251-262
[8]   SOCS1, SOCS3, and PIAS1 Promote Myogenic Differentiation by Inhibiting the Leukemia Inhibitory Factor-Induced JAK1/STAT1/STAT3 Pathway [J].
Diao, Yarui ;
Wang, Xi ;
Wu, Zhenguo .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (18) :5084-5093
[9]   ENHANCED IN-VIVO GROWTH AND RESISTANCE TO REJECTION OF TUMOR-CELLS EXPRESSING DOMINANT-NEGATIVE IFN-GAMMA RECEPTORS [J].
DIGHE, AS ;
RICHARDS, E ;
OLD, LJ ;
SCHREIBER, RD .
IMMUNITY, 1994, 1 (06) :447-456
[10]  
Dormond O, 2002, ANTICANCER RES, V22, P3159