A discrete subpopulation of dendritic cells transports apoptotic intestinal epithelial cells to T cell areas of mesenteric lymph nodes

被引:726
作者
Huang, FP [1 ]
Platt, N [1 ]
Wykes, M [1 ]
Major, JR [1 ]
Powell, TJ [1 ]
Jenkins, CD [1 ]
MacPherson, GG [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金;
关键词
rat; lymph; esterase; self tolerance; oral tolerance;
D O I
10.1084/jem.191.3.435
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This study identifies a dendritic cell (DC) subset that constitutively transports apoptotic intestinal epithelial cell, remnants to T cell areas of mesenteric lymph nodes in vivo. Rat intestinal lymph contains two DC populations. Both populations have typical DC morphology, are major histocompatibility complex class IIhi, and express OX62, CD11c, and B7. CD4(+)/OX41(+) DCs are strong antigen-presenting cells (APCs). CD4(-)/OX41(-) DCs are weak APCs and contain cytoplasmic apoptotic DNA, epithelial cell-restricted cytokeratins, and nonspecific esterase (NSE)(+) inclusions. not seen in OX41(+) DCs. Identical patterns of NSE electrophoretic variants exist in CD4(-)/OX41(-) DCs, intestinal epithelial cells, and mesenteric node DCs but not in other DC populations, macrophages, or tissues. Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick-end labeling (TUNEL)-positive DCs and strongly NSE+ DCs are present in intestinal lamina propria. Peyer's patches and mesenteric but not other lymph nodes contain many strongly NSE+ DCs in interfollicular and T cell areas. Similar DCs are seen in the ileum and in T cell areas of mesenteric nodes in gnotobiotic rats. These results show that a distinct DC subset constitutively endocytoses and transports apoptotic cells to T cell areas and suggest a role for these DCs in inducing and maintaining peripheral self-tolerance.
引用
收藏
页码:435 / 443
页数:9
相关论文
共 50 条
[1]  
Adams S, 1998, J IMMUNOL, V161, P1853
[2]   CD4+ T cell tolerance to parenchymal self-antigens requires presentation by bone marrow-derived antigen-presenting cells [J].
Adler, AJ ;
Marsh, DW ;
Yochum, GS ;
Guzzo, JL ;
Nigam, A ;
Nelson, WG ;
Pardoll, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (10) :1555-1564
[3]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[4]   Immature dendritic cells phagocytose apoptotic cells via αvβ5 and CD36, and cross-present antigens to cytotoxic T lymphocytes [J].
Albert, ML ;
Pearce, SFA ;
Francisco, LM ;
Sauter, B ;
Roy, P ;
Silverstein, RL ;
Bhardwaj, N .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (07) :1359-1368
[5]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[6]   ES-6, A FURTHER POLYMORPHIC ESTERASE IN THE RAT [J].
BENDER, K ;
NAGEL, M ;
GUNTHER, E .
BIOCHEMICAL GENETICS, 1982, 20 (3-4) :221-228
[7]  
Bocking A, 1976, Histochemistry, V50, P65, DOI 10.1007/BF00492787
[8]  
CHANDLER JS, 1991, J BIOL CHEM, V266, P11932
[9]   DENDRITIC CELLS ARE THE PRINCIPAL CELLS IN MOUSE SPLEEN BEARING IMMUNOGENIC FRAGMENTS OF FOREIGN PROTEINS [J].
CROWLEY, M ;
INABA, K ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) :383-386
[10]  
CUMBERBATCH M, 1992, IMMUNOLOGY, V75, P257