T cell regulation of hematopoiesis

被引:14
作者
Dent, Alexander L. [1 ,2 ]
Kaplan, Mark H. [1 ,2 ,3 ]
机构
[1] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Pediat, Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
T cell; cytokine; Th1; Th2; Th17; NKT; CD8; treg; inflammation; REview;
D O I
10.2741/3150
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
It has long been known that thymus-derived lymphocytes (T cells) can produce cytokines that have powerful effects on hematopoiesis. All major classes of T cells-- CD4 T helper cells, CD4 regulatory T cells, CD8 T cells, gamma delta T cells and NKT cells-- produce a number of cytokines and chemokines that can modulate hematopoiesis. More recent research has shown that specific T helper cell types, such as Th1, Th2 and Th17 cells, with the development of each subset depending on distinct STAT proteins, have the potential to modulate the hematopoietic response in different ways. In a teleological sense, the overall orchestration of the immune response by T helper cells fits with the concept that T helper cells would modulate the production of cells of the innate immune system by regulating hematopoiesis. Here we will review the literature on how T cell subsets regulate hematopoietic cell differentiation, and discuss how this regulation may complement the specific function of the T cell type.
引用
收藏
页码:6229 / 6236
页数:8
相关论文
共 71 条
  • [31] Hematopoietic growth factors, signaling and the chronic myeloproliferative disorders
    Kaushansky, Kenneth
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2006, 17 (06) : 423 - 430
  • [32] Regulation of hematopoiesis in vitro and in vivo by invariant NKT cells
    Kotsianidis, L
    Silk, JD
    Spanoudakis, E
    Patterson, S
    Almeida, A
    Schmidt, RR
    Tsatalas, C
    Bourikas, G
    Cerundolo, V
    Roberts, IAG
    Karadimitris, A
    [J]. BLOOD, 2006, 107 (08) : 3138 - 3144
  • [33] KRONENBERG M, 2003, CRIT REV IMMUNOL, V23, P403
  • [34] TGF-β signaling-deficient hematopoietic stem cells have normal self-renewal and regenerative ability in vivo despite increased proliferative capacity in vitro
    Larsson, J
    Blank, U
    Helgadottir, H
    Björnsson, JM
    Ehinger, M
    Goumans, MJ
    Fan, XL
    Levéen, P
    Karlsson, S
    [J]. BLOOD, 2003, 102 (09) : 3129 - 3135
  • [35] STAT3 is a negative regulator of granulopoiesis but is not required for G-CSF-dependent differentiation
    Lee, CK
    Raz, R
    Gimeno, R
    Gertner, R
    Wistinghausen, B
    Takeshita, K
    DePinho, RA
    Levy, DE
    [J]. IMMUNITY, 2002, 17 (01) : 63 - 72
  • [36] Li L, 1997, J IMMUNOL, V158, P4152
  • [37] Deregulated TGF-β signaling in leukemogenesis
    Lin, HK
    Bergmann, S
    Pandolfi, PP
    [J]. ONCOGENE, 2005, 24 (37) : 5693 - 5700
  • [38] BCL6b mediates the enhanced magnitude of the secondary response of memory CD8+ T lymphocytes
    Manders, PM
    Hunter, PJ
    Telaranta, AI
    Carr, JM
    Marshall, JL
    Carrasco, M
    Murakami, Y
    Palmowski, MJ
    Cerundolo, V
    Kaech, SM
    Ahmed, R
    Fearon, DT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (21) : 7418 - 7425
  • [39] Stat3 and Stat4 direct development of IL-17-secreting Th cells
    Mathur, Anubhav N.
    Chang, Hua-Chen
    Zisoulis, Dimitrios G.
    Stritesky, Gretta L.
    Yu, Qing
    O'Malley, John T.
    Kapur, Reuben
    Levy, David E.
    Kansas, Geoffrey S.
    Kaplan, Mark H.
    [J]. JOURNAL OF IMMUNOLOGY, 2007, 178 (08) : 4901 - 4907
  • [40] MILLER KL, 1992, EXP HEMATOL, V20, P951