© The Rockefeller University Press, 0022-1007/1997/7/199/ $5.00
The Journal of Experimental Medicine, Volume 186, Number 2, July 21, 1997 199-207
The Human C3a Receptor Is Expressed on Neutrophils and Monocytes, but Not on B or T Lymphocytes
Ulrich Martin*,
Daniel Bock*,
Lubomir Arseniev
,
Mark A. Tornetta
,
Robert S. Ames
,
Wilfried Bautsch*,
Jörg Köhl*,
Arnold Ganser
, and
Andreas Klos*
From the * Institute of Medical Microbiology, Hannover Medical School; the
Department of Hematology and Oncology, Hannover, 30625, Germany; and the
Department of Molecular Immunology, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406-0939
The pathophysiological relevance of the complement split product C3a as a proinflammatory mediator is still ill defined. The expression pattern of the human C3a receptor (C3aR) can provide important clues for the role of this anaphylatoxin in inflammation. There is strong evidence for C3aR expression on basophils, and eosinophils, but additionally, only on tumor cell lines of leukemic or hepatic origin. It is unclear whether neutrophils also express the C3aR, but need a costimulus provided by eosinophils for certain biological responses, or whether neutrophils lack the C3aR and respond to C3a via a secondary stimulus generated by eosinophils, i.e., by an indirect mode. In the present study, polyclonal antiserum raised against the second extracellular loop of the C3aR was used to characterize C3aR expression on peripheral blood leukocytes. For high degree purification of neutrophils, a negative selection method was established that decreased the contamination with CD9bright+ eosinophils down to <0.2%. Flow cytometric analyses, functional assays, and binding assays on highly purified neutrophils confirmed C3aR expression and coupling. Monocytes were identified as an additional C3aR-positive cell population of the peripheral blood. The expression of the C3aR on eosinophils could be confirmed. In contrast, the receptor could not be detected on unchallenged B or T lymphocytes (or lymphocyte-derived Raji cells).
Address corespondence to Andreas Klos, M.D., Institute of Medical Microbiology, Building, I6, Room 05-2410, Hannover Medical School, Hannover, 30625, Germany. Phone: 511-532-4342; FAX: 511-532-4366; E-mail: KLOS{at}MIKROBIO.MH-Hannover.de
1 Abbreviations used in this paper: C3a, an anaphylatoxic peptide generated from the complement component C3; C3aR, C3a receptor; [Ca2+]i, concentration of free cytosolic Ca2+, GAPDH, rat glyceraldehyde-3-phosphate dehydrogenase used as housekeeping gene.

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