| Literature DB >> 21948982 |
Karine Crozat1, Samira Tamoutounour, Thien-Phong Vu Manh, Even Fossum, Hervé Luche, Laurence Ardouin, Martin Guilliams, Hiroaki Azukizawa, Bjarne Bogen, Bernard Malissen, Sandrine Henri, Marc Dalod.
Abstract
Subsets of dendritic cells (DCs) have been described according to their functions and anatomical locations. Conventional DC subsets are defined by reciprocal expression of CD11b and CD8α in lymphoid tissues (LT), and of CD11b and CD103 in non-LT (NLT). Spleen CD8α(+) and dermal CD103(+) DCs share a high efficiency for Ag cross-presentation and a developmental dependency on specific transcription factors. However, it is not known whether all NLT-derived CD103(+) DCs and LT-resident CD8α(+) DCs are similar despite their different anatomical locations. XCR1 was previously described as exclusively expressed on mouse spleen CD8α(+) DCs and human blood BDCA3(+) DCs. In this article, we showed that LT-resident CD8α(+) DCs and NLT-derived CD103(+) DCs specifically express XCR1 and are characterized by a unique transcriptional fingerprint, irrespective of their tissue of origin. Therefore, CD8α(+) DCs and CD103(+) DCs belong to a common DC subset which is unequivocally identified by XCR1 expression throughout the body.Entities:
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Year: 2011 PMID: 21948982 DOI: 10.4049/jimmunol.1101717
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422