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Dectin-2 is predominantly myeloid restricted and exhibits unique activation-dependent expression on maturing inflammatory monocytes elicited in vivo

  • Philip R. Taylor*
  • , Delyth M. Reid
  • , Sigrid E.M. Heinsbroek
  • , Gordon D. Brown
  • , Siamon Gordon
  • , Simon Y.C. Wong
  • *此作品的通信作者
  • University of Oxford
  • University of Cape Town

研究成果: 期刊稿件文章同行評審

122 引文 斯高帕斯(Scopus)

摘要

Dectin-2 is a recently described dendritic-cell-associated receptor, suggested to be involved in the initiation and maintenance of UV-induced tolerance. To understand the physiological relevance of the proposed functions of this C-type lectin-like receptor, we have generated monoclonal antibodies against its extracellular domain and performed a detailed study of its expression. In naive mice, Dectin-2 has a novel distribution pattern compared with other myeloid markers, but is predominantly expressed by a wide variety of tissue macrophages. Its expression was limited on dendritic cells and notably absent from brain microglia and choroid plexus or meningeal macrophages. On peripheral blood monocytes, Dectin-2 expression was very low on the surface but was transiently and markedly up-regulated on induction of inflammation in vivo using a variety of stimuli. This change in Dectin-2 expression occurs on 'inflammatory' monocytes after arrival at the inflammatory lesion as demonstrated by adoptive cell-transfer studies, and is independent of whether the macrophages elicited by the stimuli ultimately expressed Dectin-2. These observations show Dectin-2 expression to be characteristic of monocyte activation/maturation at an inflammatory lesion and provide a new perspective on the interpretation of Dectin-2 function in vivo.

原文英語
頁(從 - 到)2163-2174
頁數12
期刊European Journal of Immunology
35
發行號7
DOIs
出版狀態已出版 - 07 2005
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