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The Journal of Immunology, 2001, 167: 3570-3576.
Copyright © 2001 by The American Association of Immunologists

Molecular Cloning of F4/80-Like-Receptor, a Seven-Span Membrane Protein Expressed Differentially by Dendritic Cell and Monocyte-Macrophage Subpopulations1 ,2

Irina Caminschi3,*,{dagger}, Karen M. Lucas*,{dagger}, Meredith A. O’Keeffe*, Hubertus Hochrein{ddagger}, Yacine Laâbi*, Frank Köntgen*, Andrew M. Lew*,{dagger}, Ken Shortman*,{dagger} and Mark D. Wright§

* Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia; {dagger} Cooperative Research Centre for Vaccine Technology, Brisbane, Queensland, Australia; {ddagger} Medical Microbiology, Immunology and Hygiene, Technischen Universitat Munchen, Germany; and § Austin Research Institute, Heidelberg, Victoria, Australia

A novel dendritic cell (DC) surface molecule termed F4/80-like-receptor (FIRE) has been selected based on its differential expression between DC subsets. The gene encoding FIRE has been cloned and sequenced, and mAbs specific for FIRE have been produced. FIRE is a seven-transmembrane-spanning molecule with two epidermal growth factor-like domains in the extracellular region. It is a novel member of the epidermal growth factor/transmembrane-7 protein subfamily and shows similarity to the macrophage marker F4/80. FIRE is expressed by CD8- DC, but not by CD8+ DC, and it is down-regulated on DC activation. It is expressed by blood monocytes and by some tissue macrophages, but not by most macrophage cell lines or by lymphoid cells. FIRE is a useful marker of myeloid cells with a DC developmental potential.




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