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Published Online May 10, 2001 Science
DOI: 10.1126/science.1056594
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Research Articles
Submitted on October 16, 2000
Accepted on April 25, 2001
Physiological Regulation of the Immunological Synapse by Agrin
Adil A. Khan 1*,
Christian Bose 2,
Lung S. Yam 2,
Mark J. Soloski 3,
Fabio Rupp 4
1 Outer Banks Neuroscience, Baltimore, MD 21218, USA; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, 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.
4 Hyseq Inc., Sunnyvale, CA 94085, USA; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
* To whom correspondence should be addressed. E-mail: outerbanksneuro{at}yahoo.com.
T cell activation is dependent on both a primary signal delivered through the T cell receptor (TCR) and a secondary costimulatory signal mediated by co-receptors. While 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 (APC). This has been termed the immunological synapse. Though essential for T cell activation, endogenous mediators of raft clustering in lymphocytes have not been identified. 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.
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