CD8α+ dendritic cells originate from the CD8α- dendritic cell subset by a maturation process involving CD8α, DEC-205, and CD24 up-regulation

被引:90
作者
del Hoyo, GM [1 ]
Martín, P [1 ]
Arias, CF [1 ]
Marín, AR [1 ]
Ardavín, C [1 ]
机构
[1] Univ Complutense, Dept Cell Biol, Fac Biol, E-28040 Madrid, Spain
关键词
D O I
10.1182/blood.V99.3.999
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
CD8alpha(+) and CD8alpha(-) dendritic cells (DCs) have been considered as independent DC subpopulations both ontogenetically and functionally during recent years. However, it has been demonstrated that both DC subsets can be generated from a single precursor population, supporting the concept that they do not represent separate DC lineages. By using highly purified splenic CD8alpha(-) DCs, which were injected intravenously and traced by means of an Ly5.1/Ly5.2 transfer system, this study shows that CD8alpha(-) DCs acquired the phenotypic characteristics of CD8alpha(+) DCs, by a differentiation process involving CD8alpha, DEC-205, and CD24 up-regulation, paralleled by the down-regulation of CD11b, F4/80, and CD4. These data demonstrate that CD8alpha(+) DCs derive from CD8alpha(-) DCs, and strongly support that CD8alpha(-) and CD8alpha(+) DCs represent different maturation or differentiation stages of the same DC population. Therefore, CD8alpha(+) DCs would represent the last stage of DC differentiation, playing an essential role in the induction of T-cell responses, due to their antigen-presenting potential, cross-priming ability, and capacity to secrete large amounts of key cytokines such as interferon gamma and interleukin-12. (C) 2002 by The American Society of Hematology.
引用
收藏
页码:999 / 1004
页数:6
相关论文
共 31 条
[1]
CCR5 provides a signal for microbial induced production of IL-12 by CD8α+ dendritic cells [J].
Aliberti, J ;
Sousa, CRE ;
Schito, M ;
Hieny, S ;
Wells, T ;
Huffnagle, GB ;
Sher, A .
NATURE IMMUNOLOGY, 2000, 1 (01) :83-87
[2]
Definition of dendritic cell subpopulations present in the spleen, Peyer's patches, lymph nodes, and skin of the mouse [J].
Anjuère, F ;
Martín, P ;
Ferrero, I ;
Fraga, ML ;
del Hoyo, GM ;
Wright, N ;
Ardavin, C .
BLOOD, 1999, 93 (02) :590-598
[3]
Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[4]
Crowley MT, 1999, J IMMUNOL, V163, P4894
[5]
CD8+ but not CD8- dendritic cells cross-prime cytotoxic T cells in vivo [J].
den Haan, JMM ;
Lehar, SM ;
Bevan, MJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (12) :1685-1695
[6]
Regulation of dendritic cell numbers and maturation by lipopolysaccharide in vivo [J].
DeSmedt, T ;
Pajak, B ;
Muraille, E ;
Lespagnard, L ;
Heinen, E ;
DeBaetselier, P ;
Urbain, J ;
Leo, O ;
Moser, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (04) :1413-1424
[7]
Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites [J].
Dieu, MC ;
Vanbervliet, B ;
Vicari, A ;
Bridon, JM ;
Oldham, E ;
Aït-Yahia, S ;
Brière, F ;
Zlotnik, A ;
Lebecque, S ;
Caux, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (02) :373-386
[8]
Macrophage inflammatory protein 3α is expressed at inflamed epithelial surfaces and is the most potent chemokine known in attracting Langerhans cell precursors [J].
Dieu-Nosjean, MC ;
Massacrier, C ;
Homey, B ;
Vanbervliet, B ;
Pin, JJ ;
Vicari, A ;
Lebecque, S ;
Dezutter-Dambuyant, C ;
Schmitt, D ;
Zlotnik, A ;
Caux, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :705-717
[9]
CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs [J].
Förster, R ;
Schubel, A ;
Breitfeld, D ;
Kremmer, E ;
Renner-Müller, I ;
Wolf, E ;
Lipp, M .
CELL, 1999, 99 (01) :23-33
[10]
PU.1 is required for myeloid-derived but not lymphoid-derived dendritic cells [J].
Guerriero, A ;
Langmuir, PB ;
Spain, LM ;
Scott, EW .
BLOOD, 2000, 95 (03) :879-885