help button home button
AJRCMB
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on June 25, 2004, doi:10.1165/rcmb.2004-0099OC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
2004-0099OCv1
31/4/413    most recent
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Johansson, M. W.
Right arrow Articles by Mosher, D. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Johansson, M. W.
Right arrow Articles by Mosher, D. F.
American Journal of Respiratory Cell and Molecular Biology. Vol. 31, pp. 413-422, 2004
© 2004 American Thoracic Society
DOI: 10.1165/rcmb.2004-0099OC

Eosinophils Adhere to Vascular Cell Adhesion Molecule-1 via Podosomes

Mats W. Johansson, Ming H. Lye, Steven R. Barthel, Allison K. Duffy, Douglas S. Annis and Deane F. Mosher

Departments of Medicine and Biomolecular Chemistry, University of Wisconsin, Madison, Wisconsin

Address correspondence to: Mats W. Johansson, Ph.D., Department of Medicine, University of Wisconsin, 4285A, Medical Sciences Center, 1300 University Avenue, Madison, WI 53706-1532. E-mail: mwj{at}medicine.wisc.edu

Vascular cell adhesion molecule (VCAM)-1 supports specific eosinophil adhesion via {alpha}4ß1 integrin. We tested the hypothesis that adhesive contacts formed by eosinophils on VCAM-1 are different from focal adhesions formed by adherent fibroblasts. Eosinophils adherent on VCAM-1 formed punctate adhesions that fit the criteria for podosomes, highly dynamic structures found in adherent transformed fibroblasts, osteoclasts, and macrophages. The structures contained ß1 integrin subunit, phosphotyrosine-containing proteins, punctate filamentous actin, and gelsolin, a podosome marker. In contrast, nontransformed fibroblasts on VCAM-1 formed peripheral focal adhesions that were positive for {alpha}4, ß1, phosphotyrosine, vinculin, talin, and paxillin; negative for gelsolin; and associated with microfilaments. Phorbol myristate acetate or tumor necrosis factor-{alpha} and interleukin-5 stimulated podosome formation in adherent eosinophils. Because podosomes in tumor cells are associated with extracellular matrix degradation, we analyzed the VCAM-1 layer. VCAM-1 was lost under adherent eosinophils but not under adherent fibroblasts. This loss was inhibited by the metalloproteinase inhibitor ortho-phenanthroline and correlated with expression and podosome localization of a membrane-tethered metalloproteinase, a disintegrin and metalloproteinase domain 8. Podosome-mediated VCAM-1 clearance may be a mechanism to regulate eosinophil arrest and extravasation in allergic conditions such as asthma.

Abbreviations: a disintegrin and metalloprotease, ADAM • bovine serum albumin, BSA • cluster of differentiation, CD • Chinese hamster ovary, CHO • fluorescence-activated cell sorting, FACS • filamentous actin, F-actin • fetal bovine serum, FBS • fluorescein isothiocyanate, FITC • formyl-methionylleucylphenylalanine, FMLP • fibronectin, FN • granulocyte-macrophage–colony stimulating factor, GM-CSF • 12(S)-hydroxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid, 12(S)-HETE • intercellular cell adhesion molecule, ICAM • immunoglobulin, Ig • interleukin, IL • monoclonal antibody, mAb • matrix metalloproteinase, MMP • ortho-phenanthroline, OP • platelet activating factor, PAF • pAcGP67.coco plasmid, pCOCO • phosphate-buffered saline, PBS • phorbol myristate acetate, PMA • phenylmethylsulfonyl fluoride, PMSF • transforming protein of Rous sarcoma virus, Src • Tris-buffered saline, TBS • tumor necrosis factor, TNF • vascular cell adhesion molecule, VCAM




This article has been cited by other articles:


Home page
J. Immunol.Home page
L. H. Ulfman, V. M. Kamp, C. W. van Aalst, L. P. Verhagen, M. E. Sanders, K. A. Reedquist, M. Buitenhuis, and L. Koenderman
Homeostatic Intracellular-Free Ca2+ Is Permissive for Rap1-Mediated Constitutive Activation of {alpha}4 Integrins on Eosinophils
J. Immunol., April 15, 2008; 180(8): 5512 - 5519.
[Abstract] [Full Text] [PDF]


Home page
J. Leukoc. Biol.Home page
S. R. Barthel, M. W. Johansson, D. M. McNamee, and D. F. Mosher
Roles of integrin activation in eosinophil function and the eosinophilic inflammation of asthma
J. Leukoc. Biol., January 1, 2008; 83(1): 1 - 12.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
K. Szczur, H. Xu, S. Atkinson, Y. Zheng, and M.-D. Filippi
Rho GTPase CDC42 regulates directionality and random movement via distinct MAPK pathways in neutrophils
Blood, December 15, 2006; 108(13): 4205 - 4213.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. R. Barthel, D. S. Annis, D. F. Mosher, and M. W. Johansson
Differential Engagement of Modules 1 and 4 of Vascular Cell Adhesion Molecule-1 (CD106) by Integrins {alpha}4beta1 (CD49d/29) and {alpha}Mbeta2 (CD11b/18) of Eosinophils
J. Biol. Chem., October 27, 2006; 281(43): 32175 - 32187.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
S. R. Barthel, N. N. Jarjour, D. F. Mosher, and M. W. Johansson
Dissection of the Hyperadhesive Phenotype of Airway Eosinophils in Asthma
Am. J. Respir. Cell Mol. Biol., September 1, 2006; 35(3): 378 - 386.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
H. Ohtsu, P. J. Dempsey, and S. Eguchi
ADAMs as mediators of EGF receptor transactivation by G protein-coupled receptors
Am J Physiol Cell Physiol, July 1, 2006; 291(1): C1 - C10.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
C. Varon, F. Tatin, V. Moreau, E. Van Obberghen-Schilling, S. Fernandez-Sauze, E. Reuzeau, I. Kramer, and E. Genot
Transforming Growth Factor {beta} Induces Rosettes of Podosomes in Primary Aortic Endothelial Cells.
Mol. Cell. Biol., May 1, 2006; 26(9): 3582 - 3594.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2004 American Thoracic Society.
  ATS Best of the Web