Journal of Leukocyte Biology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


A more recent version of this article appeared on May 1, 2004

Published online before print February 3, 2004
This Article
Right arrow Full Text (Reprint (PDF))
Right arrow All Versions of this Article:
jlb.0903408v1
75/5/910    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 Palmeri, D.
Right arrow Articles by Hemmerich, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Palmeri, D.
Right arrow Articles by Hemmerich, S.
© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.0903408


Received for publication September 1, 2003.
Revised December 2, 2003.
Accepted for publication December 14, 2003.


Article

Differential gene expression profile of human tonsil high endothelial cells: implications for lymphocyte trafficking

Diana Palmeri *@, Feng-Rong Zuo {dagger}, Steven D. Rosen *, and Stefan Hemmerich {dagger}

*Department of Anatomy and Program of Immunology, University of California, San Francisco; and {dagger}Inflammatory Diseases Unit, Roche Bioscience, Palo Alto, California

@ To whom correspondence should be addressed. E-mail: stefan{at}thiospharm.com.


   Abstract

Lymphocyte recirculation is dependent on the interactions of adhesion and signaling molecules expressed on lymphocytes and their partners on high endothelial cells (HEC). Many of the events in this process have yet to be molecularly characterized. To identify novel HEC-specific proteins with potential function in the recruitment cascade, we sequenced a normalized human tonsil HEC cDNA library (generated from an inflamed tonsil) from which lymphocyte and human umbilical vein endothelial cell cDNAs had been subtracted. One-thousand forty-nine sequences were analyzed. All but three mapped to known cDNAs or genomic DNAs. The two most abundant transcripts encoded {alpha}2-macroglobulin and hevin. The next-abundant transcripts encoded several other protease inhibitors, making this protein class the most prominent in HEC. Several endothelial-specific transcripts were also identified, including those encoding E-selectin, vascular cell adhesion molecule-1, vascular endothelial-junctional adhesion molecule, and platelet-endothelial cell adhesion molecule-1. The library contains a great diversity of transcripts, and studies of the encoded proteins will provide further insight into the complex biology of these specialized endothelial cells.

Key Words: cell adhesion • cell trafficking • lymphocyte homing • expressed sequence tags




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
V. Carriere, L. Roussel, N. Ortega, D.-A. Lacorre, L. Americh, L. Aguilar, G. Bouche, and J.-P. Girard
IL-33, the IL-1-like cytokine ligand for ST2 receptor, is a chromatin-associated nuclear factor in vivo
PNAS, January 2, 2007; 104(1): 282 - 287.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
H. S. Carlsen, G. Haraldsen, P. Brandtzaeg, and E. S. Baekkevold
Disparate lymphoid chemokine expression in mice and men: no evidence of CCL21 synthesis by human high endothelial venules
Blood, July 15, 2005; 106(2): 444 - 446.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2004 by the Society for Leukocyte Biology.