The Journal of Experimental Medicine
Avanti Polar Lipids, Inc.
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Published online 2 October 2000.
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© The Rockefeller University Press, 0022-1007/2000/10/1069/ $5.00
The Journal of Experimental Medicine, Volume 192, Number 7, October 2, 2000 1069-1074


Brief Definitive Report

Ll-37, the Neutrophil Granule–And Epithelial Cell–Derived Cathelicidin, Utilizes Formyl Peptide Receptor–Like 1 (Fprl1) as a Receptor to Chemoattract Human Peripheral Blood Neutrophils, Monocytes, and T Cells

De Yanga, Qian Chena, Albert P. Schmidtc, G. Mark Andersonc, Ji Ming Wanga, Joseph Wootersd, Joost J. Oppenheima, and Oleg Chertovb

a Laboratory of Molecular Immunoregulation, Division of Basic Sciences,
b Intramural Research Support Program, Science Applications International Corporation, Frederick, National Cancer Institute-Frederick Cancer Research and Development Center, National Institutes of Health, Frederick, Maryland 21702-1201
c Magainin Pharmaceuticals Incorporated, Plymouth Meeting, Pennsylvania 19462
d Genetics Institute, Cambridge, Massachusetts 02140
SAIC, IRSP, NCI-FCRDC, Bldg. 560, Rm. 31-19, Frederick, MD 21702-1201.301-846-7042301-846-1347

We have previously shown that antimicrobial peptides like defensins have the capacity to mobilize leukocytes in host defense. LL-37 is the cleaved antimicrobial 37-residue, COOH-terminal peptide of hCAP18 (human cationic antimicrobial protein with a molecular size of 18 kD), the only identified member in humans of a family of proteins called cathelicidins. LL-37/hCAP18 is produced by neutrophils and various epithelial cells. Here we report that LL-37 is chemotactic for, and can induce Ca2+ mobilization in, human monocytes and formyl peptide receptor–like 1 (FPRL1)-transfected human embryonic kidney 293 cells. LL-37–induced Ca2+ mobilization in monocytes can also be cross-desensitized by an FPRL1-specific agonist. Furthermore, LL-37 is also chemotactic for human neutrophils and T lymphocytes that are known to express FPRL1. Our results suggest that, in addition to its microbicidal activity, LL-37 may contribute to innate and adaptive immunity by recruiting neutrophils, monocytes, and T cells to sites of microbial invasion by interacting with FPRL1.

Key Words: cathelicidin • hCAP18 • chemotaxis • phagocyte • lymphocyte


The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government.

© 2000 The Rockefeller University Press


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