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The T cell surface--how well do we know it?

Authors :
Simon J. Davis
Lawrence Hene
Sarah Rowland-Jones
Andrew J. McMichael
R Manso-Sancho
Christelle Retière
Veronique M. Braud
Jill Powell
Tao Dong
Lisa M. Sparks
Edward J. Evans
J A Fennelly
Nuffield Department of Clinical Medicine [Oxford]
University of Oxford [Oxford]
Medical Research Council Human Immunology Unit
University of Oxford [Oxford]- John Radcliffe Hospital [Oxford University Hospital]
Cancer Research UK Laboratory
Guy's and St Thomas' Hospital [London]-Rayne Institute
Institut de pharmacologie moléculaire et cellulaire (IPMC)
Université Nice Sophia Antipolis (... - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)
Source :
Immunity, Immunity, Elsevier, 2003, 19 (2), pp.213-23
Publication Year :
2003

Abstract

The overall degree of complexity of the T cell surface has been unclear, constraining our understanding of its biology. Using global gene expression analysis, we show that 111 of 374 genes encoding well-characterized leukocyte surface antigens are expressed by a resting cytotoxic T cell. Unexpectedly, of 97 stringently defined, T cell-specific transcripts with unknown functions that we identify, none encode proteins with the modular architecture characteristic of 80% of leukocyte surface antigens. Only two encode proteins with membrane topologies found exclusively in cell surface molecules. Our analysis indicates that the cell type-specific composition of the resting CD8+ T cell surface is now largely defined, providing an insight into the overall compositional complexity of the mammalian cell surface and a framework for formulating systematic models of T cell surface-dependent processes, such as T cell receptor triggering.

Details

ISSN :
10747613
Volume :
19
Issue :
2
Database :
OpenAIRE
Journal :
Immunity
Accession number :
edsair.doi.dedup.....723918ee1b67808874e6178aeb87acde