Foxo in the immune system

被引:92
作者
Peng, S. L. [1 ]
机构
[1] Clin Res & Exploratory Dev, Palo Alto, CA 94304 USA
关键词
transcription factors; autoimmunity; T cells; B cells; arthritis; lupus;
D O I
10.1038/onc.2008.26
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In addition to their key roles in cellular survival, death, proliferation and metabolism, the Foxo subfamily of forkhead (Fox) transcription factors play critical roles in the homeostasis of immune-relevant cells, including T cells, B cells, neutrophils and other non-lymphoid lineages that modulate inflammation in disease states such as inflammatory arthritis and systemic lupus erythematosus. This review summarizes such current and expanding knowledge of the Foxo family members in immunity, and their potential as therapeutic targets in inflammatory disease.
引用
收藏
页码:2337 / 2344
页数:8
相关论文
共 70 条
[1]   Mitogen-activated protein kinases, Erk and p38, phosphorylate and regulate Foxo1 [J].
Asada, Sachie ;
Daitoku, Hiroaki ;
Matsuzaki, Hitomi ;
Saito, Tomoko ;
Sudo, Tatsuhiko ;
Mukai, Hidehito ;
Iwashita, Shintaro ;
Kako, Koichiro ;
Kishi, Tsutomu ;
Kasuya, Yoshitoshi ;
Fukamizu, Akiyoshi .
CELLULAR SIGNALLING, 2007, 19 (03) :519-527
[2]   GILZ, a new target for the transcription factor FoxO3, protects T lymphocytes from interleukin-2 withdrawal-induced apoptosis [J].
Asselin-Labat, ML ;
David, M ;
Biola-Vidamment, A ;
Lecoeuche, D ;
Zennaro, MC ;
Bertoglio, J ;
Pallardy, M .
BLOOD, 2004, 104 (01) :215-223
[3]   Mechanisms of disease: transcription factors in inflammatory arthritis [J].
Aud, Dee ;
Peng, Stanford L. .
NATURE CLINICAL PRACTICE RHEUMATOLOGY, 2006, 2 (08) :434-442
[4]   Cytokine-mediated FOXO3a phosphorylation suppresses FasL expression in hemopoietic cell lines: Investigations of the role of Fas in apoptosis due to cytokine starvation [J].
Behzad, Hayedeh ;
Jamil, Sarwat ;
Denny, Trisha A. ;
Duronio, Vincent .
CYTOKINE, 2007, 38 (02) :74-83
[5]   FOXO3a induces differentiation of Bcr-Abl- transformed cells through transcriptional down-regulation of Id1 [J].
Birkenkamp, Kim U. ;
Essafi, Abdelkader ;
van der Vos, Kristan E. ;
da Costa, Marco ;
Hui, Rosaline C. -Y ;
Holstege, Frank ;
Koenderman, Leo ;
Lam, Eric W. -F. ;
Coffer, Paul J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (04) :2211-2220
[6]   The induction of Bim expression in human T-cell blasts is dependent on nonapoptotic Fas/CD95 signaling [J].
Bosque, Alberto ;
Ignacio Aguilo, Juan ;
Angeles Alava, M. ;
Paz-Artal, Estela ;
Naval, Javier ;
Allende, Luis M. ;
Anel, Alberto .
BLOOD, 2007, 109 (04) :1627-1635
[7]   Protein kinase SGK mediates survival signals by phosphorylating the forkhead transcription factor FKHRL1 (FOXO3a) [J].
Brunet, A ;
Park, J ;
Tran, H ;
Hu, LS ;
Hemmings, BA ;
Greenberg, ME .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (03) :952-965
[8]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868
[9]   Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase [J].
Brunet, A ;
Sweeney, LB ;
Sturgill, JF ;
Chua, KF ;
Greer, PL ;
Lin, YX ;
Tran, H ;
Ross, SE ;
Mostoslavsky, R ;
Cohen, HY ;
Hu, LS ;
Cheng, HL ;
Jedrychowski, MP ;
Gygi, SP ;
Sinclair, DA ;
Alt, FW ;
Greenberg, ME .
SCIENCE, 2004, 303 (5666) :2011-2015
[10]   Vav1 promotes T cell cycle progression by linking TCR/CD28 costimulation to FOXO1 and p27kip1 expression [J].
Charvet, Celine ;
Canonigo, Ann Janette ;
Becart, Stephane ;
Maurer, Ulrich ;
Miletic, Ana V. ;
Swat, Wojciech ;
Deckert, Marcel ;
Altman, Amnon .
JOURNAL OF IMMUNOLOGY, 2006, 177 (08) :5024-5031