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Originally published in Science Express on 10 May 2001
Science 1 June 2001: Vol. 292. no. 5522, pp. 1681 - 1686
DOI: 10.1126/science.1056594
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Research Articles
Physiological Regulation of the Immunological Synapse by Agrin
Adil A. Khan,12*
Christian Bose,2
Lung S. Yam,2
Mark J. Soloski,3
Fabio Rupp2
T cell activation is dependent on both a primary signal delivered
through the T cell receptor and a secondary costimulatory signal
mediated by coreceptors. Although controversial, costimulation is
thought to act through the specific redistribution and clustering of
membrane and intracellular kinase-rich lipid raft microdomains at the
contact site between T cells and antigen-presenting cells. This site
has been termed the immunological synapse. Endogenous mediators of raft
clustering in lymphocytes have not been identified, although they are
essential for T cell activation. We now demonstrate that agrin, an
aggregating protein crucial for formation of the neuromuscular
junction, is also expressed in lymphocytes and is important in
reorganization of membrane lipid microdomains and setting the threshold
for T cell signaling. Our data show that agrin induces the aggregation
of signaling proteins and the creation of signaling domains in both
immune and nervous systems through a common lipid raft pathway.
1 Outer Banks Neuroscience, Baltimore, MD
21218, USA.
2 Department of Neuroscience, Johns
Hopkins University School of Medicine, Baltimore, MD 21205, USA.
3 Department of Medicine, Johns Hopkins University
School of Medicine, Baltimore, MD 21205, USA.
*
To whom correspondence should be addressed:
outerbanksneuro{at}yahoo.com
Present address: Hyseq Inc., Sunnyvale, CA 94085, USA.
Read the Full Text
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