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SCIMP, a transmembrane adaptor protein involved in major histocompatibility complex class II signaling.


ABSTRACT: Formation of the immunological synapse between an antigen-presenting cell (APC) and a T cell leads to signal generation in both cells involved. In T cells, the lipid raft-associated transmembrane adaptor protein LAT plays a central role. Its phosphorylation is a crucial step in signal propagation, including the calcium response and mitogen-activated protein kinase activation, and largely depends on its association with the SLP76 adaptor protein. Here we report the discovery of a new palmitoylated transmembrane adaptor protein, termed SCIMP. SCIMP is expressed in B cells and other professional APCs and is localized in the immunological synapse due to its association with tetraspanin-enriched microdomains. In B cells, it is constitutively associated with Lyn kinase and becomes tyrosine phosphorylated after major histocompatibility complex type II (MHC-II) stimulation. When phosphorylated, SCIMP binds to the SLP65 adaptor protein and also to the inhibitory kinase Csk. While the association with SLP65 initiates the downstream signaling cascades, Csk binding functions as a negative regulatory loop. The results suggest that SCIMP is involved in signal transduction after MHC-II stimulation and therefore serves as a regulator of antigen presentation and other APC functions.

SUBMITTER: Draber P 

PROVIDER: S-EPMC3209250 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature

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SCIMP, a transmembrane adaptor protein involved in major histocompatibility complex class II signaling.

Draber Peter P   Vonkova Ivana I   Stepanek Ondrej O   Hrdinka Matous M   Kucova Marketa M   Skopcova Tereza T   Otahal Pavel P   Angelisova Pavla P   Horejsi Vaclav V   Yeung Mandy M   Weiss Arthur A   Brdicka Tomas T  

Molecular and cellular biology 20110919 22


Formation of the immunological synapse between an antigen-presenting cell (APC) and a T cell leads to signal generation in both cells involved. In T cells, the lipid raft-associated transmembrane adaptor protein LAT plays a central role. Its phosphorylation is a crucial step in signal propagation, including the calcium response and mitogen-activated protein kinase activation, and largely depends on its association with the SLP76 adaptor protein. Here we report the discovery of a new palmitoylate  ...[more]

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