This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Akahoshi, T.
Right arrow Articles by Kondo, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Akahoshi, T.
Right arrow Articles by Kondo, H.

 Previous Article  |  Next Article 

Infection and Immunity, January 2003, p. 524-526, Vol. 71, No. 1
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.1.524-526.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Production of Macrophage Inflammatory Protein 3{alpha} (MIP-3{alpha}) (CCL20) and MIP-3ß (CCL19) by Human Peripheral Blood Neutrophils in Response to Microbial Pathogens

Tohru Akahoshi,1* Takeshi Sasahara,2 Rie Namai,3 Toshimichi Matsui,3 Hiroyuki Watabe,3 Hidero Kitasato,2 Matsuhisa Inoue,2 and Hirobumi Kondo3

Departments of Laboratory Medicine,1 Microbiology,2 Internal Medicine, Kitasato University School of Medicine, Kanagawa, Japan3

Received 11 July 2002/ Returned for modification 26 August 2002/ Accepted 4 October 2002

Effects of bacterial pathogens on the production of macrophage inflammatory protein 3{alpha} (MIP-3{alpha}) and MIP-3ß from human peripheral blood neutrophils were investigated. Neutrophils produced both chemokines by coincubation with either gram-positive or gram-negative bacteria. Neutrophils may initiate antigen-specific immune responses through the release of these chemokines that are capable of promoting selective recruitment of dendritic cells and T-cell subsets.


* Corresponding author. Mailing address: Department of Laboratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato, Sagamihara, Kanagawa 228-8555, Japan. Phone: 81-42-778-9119. Fax: 81-42-778-8441. E-mail: akahoshi{at}med.kitasato-u.ac.jp.

Editor: W. A. Petri, Jr.


Infection and Immunity, January 2003, p. 524-526, Vol. 71, No. 1
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.1.524-526.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Katchar, K., Kelly, C. P., Keates, S., O'Brien, M. J., Keates, A. C. (2007). MIP-3{alpha} neutralizing monoclonal antibody protects against TNBS-induced colonic injury and inflammation in mice. Am. J. Physiol. Gastrointest. Liver Physiol. 292: G1263-G1271 [Abstract] [Full Text]  
  • Megiovanni, A. M., Sanchez, F., Robledo-Sarmiento, M., Morel, C., Gluckman, J. C., Boudaly, S. (2006). Polymorphonuclear neutrophils deliver activation signals and antigenic molecules to dendritic cells: a new link between leukocytes upstream of T lymphocytes. J. Leukoc. Biol. 79: 977-988 [Abstract] [Full Text]  
  • Bennouna, S., Denkers, E. Y. (2005). Microbial Antigen Triggers Rapid Mobilization of TNF-{alpha} to the Surface of Mouse Neutrophils Transforming Them into Inducers of High-Level Dendritic Cell TNF-{alpha} Production. J. Immunol. 174: 4845-4851 [Abstract] [Full Text]  
  • Sack, R. A., Conradi, L., Krumholz, D., Beaton, A., Sathe, S., Morris, C. (2005). Membrane Array Characterization of 80 Chemokines, Cytokines, and Growth Factors in Open- and Closed-Eye Tears: Angiogenin and Other Defense System Constituents. IOVS 46: 1228-1238 [Abstract] [Full Text]  
  • Bennouna, S., Bliss, S. K., Curiel, T. J., Denkers, E. Y. (2003). Cross-Talk in the Innate Immune System: Neutrophils Instruct Recruitment and Activation of Dendritic Cells during Microbial Infection. J. Immunol. 171: 6052-6058 [Abstract] [Full Text]