Signaling by intrathymic cytokines, not T cell antigen receptors, specifies CD8 lineage choice and promotes the differentiation of cytotoxic-lineage T cells

被引:183
作者
Park, Jung-Hyun [1 ]
Adoro, Stanley [1 ]
Guinter, Terry [1 ]
Erman, Batu [2 ]
Alag, Amala S. [1 ]
Catalfamo, Marta [3 ]
Kimura, Motoko Y. [1 ]
Cui, Yongzhi [4 ]
Lucas, Philip J. [5 ]
Gress, Ronald E. [5 ]
Kubo, Masato [6 ]
Hennighausen, Lothar [4 ]
Feigenbaum, Lionel [7 ]
Singer, Alfred [1 ]
机构
[1] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[2] Sabanci Univ, Biol Sci & Bioengn Program, Fac Engn & Nat Sci, Istanbul, Turkey
[3] NIAID, Lab Immunoregulat, NIH, Bethesda, MD 20892 USA
[4] NIDDK, Lab Genet & Physiol, NIH, Bethesda, MD USA
[5] NCI, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA
[6] RIKEN, Yokohama Inst, Lab Signal Network, Res Ctr Allergy & Immunol, Kanagawa, Japan
[7] NCI, Sci Applicat Int Corp Frederick, Frederick Canc Res & Dev Ctr, Frederick, MD USA
基金
美国国家卫生研究院;
关键词
DOUBLE-POSITIVE THYMOCYTES; TRANSCRIPTION FACTORS; NEGATIVE SELECTION; DISTINCT FUNCTIONS; RUNX PROTEINS; THPOK; COMMITMENT; IL-7; EXPRESSION; DIRECTS;
D O I
10.1038/ni.1840
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immature CD4(+) CD8(+) (double-positive (DP)) thymocytes are signaled via T cell antigen receptors (TCRs) to undergo positive selection and become responsive to intrathymic cytokines such as interleukin 7 (IL-7). We report here that cytokine signaling is required for positively selected thymocytes to express the transcription factor Runx3, specify CD8 lineage choice and differentiate into cytotoxic-lineage T cells. In DP thymocytes genetically engineered to be cytokine responsive, IL-7 signaling induced TCR-unsignaled DP thymocytes to express Runx3 and to differentiate into mature CD8(+) T cells, completely circumventing positive selection. We conclude that TCR-mediated positive selection converts DP cells into cytokine-responsive thymocytes, but it is subsequent signaling by intrathymic cytokines that specifies CD8 lineage choice and promotes differentiation into cytotoxic-lineage T cells.
引用
收藏
页码:257 / U10
页数:9
相关论文
共 50 条
[1]   Characterization of the thymic IL-7 niche in vivo [J].
Alves, Nuno L. ;
Goff, Odile Richard-Le ;
Huntington, Nicholas D. ;
Sousa, Ana Patricia ;
Ribeiro, Vera S. G. ;
Bordack, Allison ;
Vives, Francina Langa ;
Peduto, Lucie ;
Chidgey, Ann ;
Cumano, Ana ;
Boyd, Richard ;
Eberl, Gerard ;
Di Santo, James P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (05) :1512-1517
[2]   Unraveling a revealing paradox:: Why major histocompatibility complex I-signaled thymocytes "Paradoxically" appear as CD4+8lo transitional cells during positive selection of CD8+ T cells [J].
Bosselut, R ;
Guinter, TI ;
Sharrow, SO ;
Singer, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (12) :1709-1719
[3]   Coreceptor reversal in the thymus:: Signaled CD4+8+ thymocytes initially terminate CD8 transcription even when differentiating into CD8+ T cells [J].
Brugnera, E ;
Bhandoola, A ;
Cibotti, R ;
Yu, Q ;
Guinter, TI ;
Yamashita, Y ;
Sharrow, SO ;
Singer, A .
IMMUNITY, 2000, 13 (01) :59-71
[4]   Suppressor of cytokine signaling-1 is a critical regulator of interleukin-7-dependent CD8+ T cell differentiation [J].
Chong, MMW ;
Cornish, AL ;
Darwiche, R ;
Stanley, EG ;
Purton, JF ;
Godfrey, DI ;
Hilton, DJ ;
Starr, R ;
Alexander, WS ;
Kay, TWH .
IMMUNITY, 2003, 18 (04) :475-487
[5]  
Chu DH, 1999, J IMMUNOL, V163, P2610
[6]   Inactivation of Stat5 in mouse mammary epithelium during pregnancy reveals distinct functions in cell proliferation, survival, and differentiation [J].
Cui, Y ;
Riedlinger, G ;
Miyoshi, K ;
Tang, W ;
Li, CL ;
Deng, CX ;
Robinson, GW ;
Hennighausen, L .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (18) :8037-8047
[7]   ThPOK acts late in specification of the helper T cell lineage and suppresses Runx-mediated commitment to the cytotoxic T cell lineage [J].
Egawa, Takeshi ;
Littman, Dan R. .
NATURE IMMUNOLOGY, 2008, 9 (10) :1131-1139
[8]   The role of the Runx transcription factors in thymocyte differentiation and in homeostasis of naive T cells [J].
Egawa, Takeshi ;
Tillman, Robert E. ;
Naoe, Yoshinori ;
Taniuchi, Ichiro ;
Littman, Dan R. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (08) :1945-1957
[9]   Antagonistic interplay between ThPOK and Runx in lineage choice of thymocytes [J].
Egawa, Takeshi ;
Taniuchi, Ichiro .
BLOOD CELLS MOLECULES AND DISEASES, 2009, 43 (01) :27-29
[10]   A dose effect of IL-7 on thymocyte development [J].
El Kassar, N ;
Lucas, PJ ;
Klug, DB ;
Zamisch, M ;
Merchant, M ;
Bare, CV ;
Choudhury, B ;
Sharrow, SO ;
Richie, E ;
Mackall, CL ;
Gress, RE .
BLOOD, 2004, 104 (05) :1419-1427