High levels of a major histocompatibility complex II self peptide complex on dendritic cells from the T cell areas of lymph nodes

被引:230
作者
Inaba, K
Pack, M
Inaba, M
Sakuta, H
Isdell, F
Steinman, RM
机构
[1] ROCKEFELLER UNIV,NEW YORK,NY 10021
[2] KYOTO UNIV,KYOTO 60601,JAPAN
[3] KANSAI MED UNIV,OSAKA 576,JAPAN
关键词
D O I
10.1084/jem.186.5.665
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 lymphocytes recirculate continually through the T cell areas of peripheral lymph nodes. During each passage, the T cells survey the surface of large dendritic cells (DCs), also known as interdigitating cells. However, these DCs have been difficult to release from the lymph node. By emphasizing the use of calcium-free media, as shown by Vremec et al. (Vremec, D., M. Zorbas, R. Scollay, D.J. Saunders, C.F. Ardavin, L. Wu, and K. Shortman. 1992. J. Exp. Med. 176:47-58.), we have been able to release and enrich DCs from the T cell areas. The DCs express the CD11c leukocyte integrin, the DEC-205 multilectin receptor for antigen presentation, the intracellular granule antigens which are recognized by monoclonal antibodies M342, 2A1, and MIDC-8, very high levels of MHC I and MHC II, and abundant accessory molecules such as CD40, CD54, and CD86. When examined with the Y-Ae monoclonal which recognizes complexes formed between I-A(b) and a peptide derived from I-E alpha, the T cell area DCs expressed the highest levels. The enriched DCs also stimulated a T-T hybridoma specific for this MHC II-peptide complex, and the hybridoma underwent apoptosis. Therefore DCs within the T cell areas can be isolated. Because they present very high levels of self peptides, these DCs should be considered in the regulation of self reactivity in the periphery.
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页码:665 / 672
页数:8
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