Enrichment for a CD26hi SIRP- subset in lymph dendritic cells from the upper aero-digestive tract

被引:46
作者
Epardaud, M
Bonneau, M
Payot, F
Cordier, C
Mégret, J
Howard, C
Schwartz-Cornil, I
机构
[1] INRA, UR892, F-78352 Jouy En Josas, France
[2] Ctr Rech Imagerie Intervent, Jouy En Josas, France
[3] Hop Necker Enfants Malad, INSERM, IFR94, Paris, France
[4] Inst Food Res, Inst Anim Hlth, Newbury RG16 0NN, Berks, England
关键词
cell trafficking; mucosa; tolerance; sheep;
D O I
10.1189/jlb.0404223
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dendritic cells (DC) have been reported to migrate in afferent lymph in the steady state. However, it is unknown whether DC traffic is modulated by the nature of the drained tissue. To analyze the influence of mucosal versus cutaneous microenvironments on the constitutive DC release, we exploited a novel technique of lymph cannulation in sheep, which allowed a comparison of afferent lymph DC migrating from the head mucosae [cervical DC (CerDC)] with DC migrating from skin [prescapular DC (PresDC)]. The migration rate was lower for CerDC than for PresDC. Compared with PresDC, CerDC contained a higher proportion of the CD26(hi) signal regulatory protein (SIRP)(-) DC subset. It is interesting that cytoplasmic apoptotic DNA as well as cytokeratin-positive inclusions were primarily detected among CD26(hi) SIRP- DC, an observation similar to that made in rats, which leads to the suggestion that this subset was involved in self-antigen presentation and tolerance induction. After the inoculation of cholera toxin (CT) onto the oro-nasal mucosae, migration of CD26(hi) SIRP- and CD26(lo) SIRP+ DC was accelerated in lymph, indicating that the effect of CT on DC mobilization is not subset-specific. Our results show that a mucosal environment influences DC output and the relative DiC subset representation in lymph. This modulation of DC traffic to lymph nodes by mucosal surfaces is likely to affect the bias of the mucosal immune responses.
引用
收藏
页码:553 / 561
页数:9
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