Differential effect of Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1) on leukocyte infiltration during contact hypersensitivity responses

Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, United States
Department of Pediatrics, University of Colorado Health Sciences Center, Aurora, Colorado, United States
Department of Pathology, The Johns Hopkins University, Baltimore, MD, United States
Department of Pathology, Northwestern University, Chicago, Illinois, United States
DOI
10.7287/peerj.preprints.2947v2
Subject Areas
Cell Biology, Dermatology, Immunology
Keywords
Platelet Endothelial Cell Adhesion Molecule-1, Leukocyte, Contact Hypersensitivity, Emigration, monocytes, granulocytes, γδ T lymphocytes, CD4+ T lymphocytes, Natural Killer Lymphocytes
Copyright
© 2017 Early et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Early M, Schroeder WG, Unnithan R, Gilchrist JM, Muller WA, Schenkel A. 2017. Differential effect of Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1) on leukocyte infiltration during contact hypersensitivity responses. PeerJ Preprints 5:e2947v2

Abstract

BACKGROUND: 2’-4’ Dinitrofluorobenzene (DNFB) induced contact hypersensitivity is an established model of contact sensitivity and leukocyte migration. Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1) deficient mice were used to examine the role of PECAM-1 in the migration capacity of several different leukocyte populations after primary and secondary application. RESULTS: γδ T lymphocytes, granulocytes, and Natural Killer cells were most affected by PECAM-1 deficiency at the primary site of application. γδ T lymphocytes, granulocytes, DX5+ Natural Killer cells, and, interestingly, effector CD4+ T lymphocytes were most affected by the loss of PECAM-1 at the secondary site of application. CONCLUSIONS: PECAM-1 is used by many leukocyte populations for migration, but there are clearly differential effects on the usage by each subset. Further, the overall kinetics of each population varied between primary and secondary application, with large relative increases in γδ T lymphocytes during the secondary response.

Author Comment

We've added more discussion of our findings and updated proposed future studies.

Supplemental Information

Ears Expts 1-3 + Skin Expt 1

DOI: 10.7287/peerj.preprints.2947v2/supp-1

Ear Expt 4 + Skin Expts 2-4

DOI: 10.7287/peerj.preprints.2947v2/supp-2