BLC (CXCL13) is expressed by different dendritic cell subsets in vitro andin vivo

Citation
Jlm. Vissers et al., BLC (CXCL13) is expressed by different dendritic cell subsets in vitro andin vivo, EUR J IMMUN, 31(5), 2001, pp. 1544-1549
Citations number
23
Categorie Soggetti
Immunology
Journal title
EUROPEAN JOURNAL OF IMMUNOLOGY
ISSN journal
00142980 → ACNP
Volume
31
Issue
5
Year of publication
2001
Pages
1544 - 1549
Database
ISI
SICI code
0014-2980(200105)31:5<1544:B(IEBD>2.0.ZU;2-T
Abstract
Dendritic cells (DC) attract both T and B lymphocytes to induce an efficien t antigen-specific immune response. Recently, it was shown that naive T cel ls are attracted to DC by dendritic cell chemokine 1 (DC-CK1, CCL18). The p otent B lymphocyte chemoattractant BLC (CXCL13) was previously shown to be essential for homing of lymphocytes into secondary lymphoid organs and for the development of B cell follicles. As the cells that produce BLC are larg ely unknown and BLC could be a candidate chemokine for the recruitment of B cells to DC, we analyzed different DC subsets for expression of BLC. Here we demonstrate that monocyte-derived DC as well as activated blood DC indee d express and secrete BLC. Interestingly, ligation of the CD40 molecule dow n-regulated BLC expression in monocyte-derived DC. Staining of tonsilar sec tions indicated that BLC is expressed by follicular dendritic cells and ger minal center dendritic cells (GCDC) in vivo. Real-time quantitative PCR con firmed the expression of BLC in isolated GCDC. Since both B cells and activ ated T cells express the receptor for BLC, our findings implicate an import ant role for BLC in establishing the interaction of DC with T cells and B c ells. Furthermore, CD40/CD40 ligand interactions could modulate this proces s by down-regulating the expression of BLC.