Development of CD4+ macrophages from intrathymic T cell progenitors is induced by thymic epithelial cells

被引:17
作者
Esashi, E
Ito, H
Ishihara, K
Hirano, T
Koyasu, S
Miyajima, A
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Osaka Univ, Lab Dev Immunol, Grad Sch Frontier Biosci, Suita, Osaka, Japan
[3] Osaka Univ, Grad Sch Med, Dept Mol Oncol, Suita, Osaka, Japan
[4] RIKEN, Res Ctr Allergy & Immunol, Lab Cytokine Signaling, Yokohama, Kanagawa, Japan
[5] Keio Univ, Sch Med, Dept Microbiol & Immunol, Tokyo, Japan
[6] Japan Sci & Technol Corp, Core Evolut Sci & Technol, Kawaguchi, Japan
关键词
D O I
10.4049/jimmunol.173.7.4360
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It was recently demonstrated that there are CD4(+) macrophages, which exhibit strong phagocytic activity, in the thymus. They are suggested to play an important role for the elimination of apoptotic thymocytes. However, the origin and nature of CD4(+) macrophages in the thymus remain unexplored. In this study, we describe that the most immature intrathymic progenitors (CD25(-)/CD44(+)/FcR(+)) give rise to CD4(+) macrophages by oncostatin M-responsive thymic epithelial cells.(ORTEC) in an IL-7-dependent manner. Neither conditioned medium of ORTEC nor a mixture of cytokines induced CD4(+) macrophages, and oncostatin M receptor was not expressed in thymocytes, suggesting that the development of CD4(+) macrophages from the immature thymocytes requires a direct interaction with ORTEC. These results collectively suggest that the development of CD4(+) macrophages from the intrathymic T cell progenitors is induced by thymic epithelial cells.
引用
收藏
页码:4360 / 4367
页数:8
相关论文
共 36 条
[1]   A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[2]   Bcl-2 rescues T lymphopoiesis in interleukin-7 receptor-deficient mice [J].
Akashi, K ;
Kondo, M ;
vonFreedenJeffry, U ;
Murray, R ;
Weissman, IL .
CELL, 1997, 89 (07) :1033-1041
[3]   Cellular interactions in thymocyte development [J].
Anderson, G ;
Moore, NC ;
Owen, JJT ;
Jenkinson, EJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :73-99
[4]   MHC CLASS-II-POSITIVE EPITHELIUM AND MESENCHYME CELLS ARE BOTH REQUIRED FOR T-CELL DEVELOPMENT IN THE THYMUS [J].
ANDERSON, G ;
JENKINSON, EJ ;
MOORE, NC ;
OWEN, JJT .
NATURE, 1993, 362 (6415) :70-73
[5]   A DIFFERENTIAL-AVIDITY MODEL FOR T-CELL SELECTION [J].
ASHTONRICKARDT, PG ;
TONEGAWA, S .
IMMUNOLOGY TODAY, 1994, 15 (08) :362-366
[6]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[7]   Dissociation of thymic positive and negative selection in transgenic mice expressing major histocompatibility complex class I molecules exclusively on thymic cortical epithelial cells [J].
Capone, M ;
Romagnoli, P ;
Beermann, F ;
MacDonald, HR ;
van Meerwijk, JPM .
BLOOD, 2001, 97 (05) :1336-1342
[8]  
CECCHINI MG, 1994, DEVELOPMENT, V120, P1357
[9]   Oncostatin M transforms lymphoid tissue function in transgenic mice by stimulating lymph node T-cell development and thymus autoantibody production [J].
Clegg, CH ;
Haugen, HS ;
Rulffes, JT ;
Friend, SL ;
Farr, AG .
EXPERIMENTAL HEMATOLOGY, 1999, 27 (04) :712-725
[10]   Regulation of an extrathymic T-cell development pathway by oncostatin M [J].
Clegg, CH ;
Rulffes, JT ;
Wallace, PM ;
Haugen, HS .
NATURE, 1996, 384 (6606) :261-263