Two developmentally distinct populations of dendritic cells inhabit the adult mouse thymus: Demonstration by differential importation of hematogenous precursors under steady state conditions

被引:68
作者
Donskoy, E [1 ]
Goldschneider, I [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Sch Med, Dept Pathol, Farmington, CT 06030 USA
关键词
D O I
10.4049/jimmunol.170.7.3514
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although a variety of lymphoid and myeloid precursors can generate thymic dendritic cells (DCs) under defined experimental conditions, the developmental origin(s) of DCs in the steady state thymus is unknown. Having previously used selective combinations of normal, parabiotic, and radioablated mice to demonstrate that blood-borne prothymocytes are imported in a gated and competitive manner, we used a similar approach in this study. to investigate the importation of the hematogenous precursors of thymic DCs. The results indicate that two developmentally distinct populations of DC precursors normally enter the adult mouse thymus. The first population is indistinguishable from prothymocytes according to the following criteria: 1) inefficient (<20%) exchange between parabiotic partners; 2) gated importation by the thymus; 3) competitive antagonism for intrathymic niches; 4) temporally linked generation of thymocytes and CD8 alpha(high) DCs; and 5) absence from prothymocyte-poor blood samples. The second population differs diametrically from prothymocytes in each of these properties, and appears to enter the thymus in at least a partially differentiated state. The resulting population of DC has a CD8 alpha(-/low) phenotype, and constitutes similar to 50% of total thymic DCs. The presence of two discrete populations of DCs in the steady state thymus implies functional heterogeneity consistent with evidence implicating lymphoid DCs in the negative selection of effector thymocytes and myeloid DCs in the positive selection of regulatory thymocytes.
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页码:3514 / 3521
页数:8
相关论文
共 48 条
[1]   Delineation of intrathymic T, NK, and dendritic cell (DC) progenitors in fetal and adult rats:: Demonstration of a bipotent T/DC intermediate precursor [J].
Alonso, LM ;
Muñoz, JJ ;
Zapata, AG .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3635-3641
[2]   Origin and differentiation of dendritic cells [J].
Ardavín, C ;
del Hoyo, GM ;
Martín, P ;
Anjuère, F ;
Arias, CF ;
Marín, AR ;
Ruiz, S ;
Parrillas, V ;
Hernández, H .
TRENDS IN IMMUNOLOGY, 2001, 22 (12) :691-700
[3]   THYMIC DENDRITIC CELLS AND T-CELLS DEVELOP SIMULTANEOUSLY IN THE THYMUS FROM A COMMON PRECURSOR POPULATION [J].
ARDAVIN, C ;
WU, L ;
LI, CL ;
SHORTMAN, K .
NATURE, 1993, 362 (6422) :761-763
[4]   Human thymus contains IFN-α-producing CD11c-, myeloid CD11c+ and mature interdigitating dendritic cells [J].
Bendriss-Vermare, N ;
Barthélémy, C ;
Durand, I ;
Bruand, C ;
Dezutter-Dambuyant, C ;
Moulian, N ;
Berrih-Aknin, S ;
Caux, C ;
Trinchieri, G ;
Brière, F .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (07) :835-844
[5]  
Beschorner WE, 1995, TRANSPLANTATION, V60, P1326
[6]  
Björck P, 1998, J IMMUNOL, V161, P5795
[7]   Targeted expression of major histocompatibility complex (MHC) class II molecules demonstrates that dendritic cells can induce negative but not positive selection of thymocytes in vivo [J].
Brocker, T ;
Riedinger, M ;
Karjalainen, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (03) :541-550
[8]   THE FAILURE OF INTRATHYMIC TRANSPLANTATION OF NONIMMUNOGENIC ISLET ALLOGRAFTS TO PROMOTE INDUCTION OF DONOR-SPECIFIC UNRESPONSIVENESS [J].
CAMPOS, L ;
POSSELT, AM ;
DELI, BC ;
MAYO, GL ;
PETE, K ;
BARKER, CF ;
NAJI, A .
TRANSPLANTATION, 1994, 57 (06) :950-953
[9]   Role for thymic and splenic regulatory CD4+ T cells induced by donor dendritic cell sin allograft tolerance by LF15-0195 treatment [J].
Chiffoleau, E ;
Bériou, G ;
Dutartre, P ;
Usal, C ;
Soulillou, JP ;
Cuturi, MC .
JOURNAL OF IMMUNOLOGY, 2002, 168 (10) :5058-5069
[10]   CD8α+ dendritic cells originate from the CD8α- dendritic cell subset by a maturation process involving CD8α, DEC-205, and CD24 up-regulation [J].
del Hoyo, GM ;
Martín, P ;
Arias, CF ;
Marín, AR ;
Ardavín, C .
BLOOD, 2002, 99 (03) :999-1004