| Literature DB >> 15905497 |
Shalin H Naik1, Anna I Proietto, Nicholas S Wilson, Aleksandar Dakic, Petra Schnorrer, Martina Fuchsberger, Mireille H Lahoud, Meredith O'Keeffe, Qi-xiang Shao, Wei-feng Chen, José A Villadangos, Ken Shortman, Li Wu.
Abstract
We demonstrate that functional and phenotypic equivalents of mouse splenic CD8(+) and CD8(-) conventional dendritic cell (cDC) subsets can be generated in vitro when bone marrow is cultured with fms-like tyrosine kinase 3 (flt3) ligand. In addition to CD45RA(high) plasmacytoid DC, two distinct CD24(high) and CD11b(high) cDC subsets were present, and these subsets showed equivalent properties to splenic CD8(+) and CD8(-) cDC, respectively, in the following: 1) surface expression of CD11b, CD24, and signal regulatory protein-alpha; 2) developmental dependence on, and mRNA expression of, IFN regulatory factor-8; 3) mRNA expression of TLRs and chemokine receptors; 4) production of IL-12 p40/70, IFN-alpha, MIP-1alpha, and RANTES in response to TLR ligands; 5) expression of cystatin C; and 6) cross-presentation of exogenous Ag to CD8 T cells. Furthermore, despite lacking surface CD8 expression, the CD24(high) subset contained CD8 mRNA and up-regulated surface expression when transferred into mice. This culture system allows access to bona fide counterparts of the splenic DC subsets.Entities:
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Year: 2005 PMID: 15905497 DOI: 10.4049/jimmunol.174.11.6592
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422