Controlling the thymic microenvironment

被引:70
作者
Gray, DHD
Ueno, T
Chidgey, AP
Malin, M
Goldberg, GL
Takahama, Y
Boyd, RL [1 ]
机构
[1] Monash Univ, Cent & Eastern Clin Sch, Dept Immunol, Melbourne, Vic 3181, Australia
[2] Univ Tokushima, Inst Genoma Res, Div Expt Immunol, Tokushima 7708503, Japan
关键词
D O I
10.1016/j.coi.2005.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell development in the thymus is a stepwise process, mediated by a variety of stromal cells in different regions of the organ. Although the cellular composition of the thymic microenvironment has been known for over a decade, the molecular cues that govern its formation are only beginning to be understood. Stromal-derived chemokines attract T-cell precursors to the thymus and direct maturing thymocytes to appropriate niches for their further development. Reciprocal signals from developing T cells provide crosstalk that is essential for establishment and maintenance of the thymic microenvironment. Elucidation of the molecular players involved and their context within the organ is the challenge for the field today. This knowledge could then be translated to clinical restoration of thymic function and T-cell reconstitution.
引用
收藏
页码:137 / 143
页数:7
相关论文
共 58 条
[1]   Lymphostromal interactions in thymic development and function [J].
Anderson, G ;
Jenkinson, EJ .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (01) :31-40
[2]   Thymic vasculature: organizer of the medullary epithelial compartment? [J].
Anderson, M ;
Anderson, SK ;
Farr, AG .
INTERNATIONAL IMMUNOLOGY, 2000, 12 (07) :1105-1110
[3]   A role of CXC chemokine ligand 12/stromal cell-derived factor-1/pre-B cell growth stimulating factor and its receptor CXCR4 in fetal and adult T cell development in vivo [J].
Ara, T ;
Itoi, M ;
Kawabata, K ;
Egawa, T ;
Tokoyoda, K ;
Sugiyama, T ;
Fujii, N ;
Amagai, T ;
Nagasawa, T .
JOURNAL OF IMMUNOLOGY, 2003, 170 (09) :4649-4655
[4]   Age-associated changes in thymopoiesis [J].
Aspinall, R ;
Andrew, D ;
Pido-Lopez, J .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 2002, 24 (01) :87-101
[5]   Disorganization of thymic medulla precedes evolution towards diabetes in female NOD mice [J].
Atlan-Gepner, C ;
Naspetti, M ;
Valéro, R ;
Barad, M ;
Lepault, F ;
Vialettes, B ;
Naquet, P .
AUTOIMMUNITY, 1999, 31 (04) :249-260
[6]   Wnt glycoproteins regulate the expression of FoxNI, the gene defective in nude mice [J].
Balciunaite, G ;
Keller, MP ;
Balciunaite, E ;
Piali, L ;
Zuklys, S ;
Mathieu, YD ;
Gill, J ;
Boyd, R ;
Sussman, DJ ;
Holländer, GA .
NATURE IMMUNOLOGY, 2002, 3 (11) :1102-1108
[7]   Identification and characterization of thymic epithelial progenitor cells [J].
Bennett, AR ;
Farley, A ;
Blair, NF ;
Gordon, J ;
Sharp, L ;
Blackburn, CC .
IMMUNITY, 2002, 16 (06) :803-814
[8]  
BENZ C, 2004, EUR J IMMUNOL
[9]   Developing a new paradigm for thymus organogenesis [J].
Blackburn, CC ;
Manley, NR .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (04) :278-289
[10]   Thymic medullary epithelial cell differentiation thymocyte emigration, and the control of autoimmunity require lymphoepithelial cross talk via LTβR [J].
Boehm, T ;
Scheu, S ;
Pfeffer, K ;
Bleul, CC .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (05) :757-769