Publication: lntegrin activation by chemokines. Relevance to inflammatory adhesion cascade during T cell migration
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Date
2000
Authors
Tanaka, Y.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
The adhesive function of integrins is
regulated through cytoplasmic signaling induced by
several stimuli, whose process is designated "inside-out
signaling". A large number of leukocytes are rapidly
recruited to the sites of inflammation where they form an
essential component of the response to infection, injury,
autoimmune disorders, allergy, tumor invasion,
atherosclerosis and so on. The recruitment of leukocytes
into tissue is regulated by a sequence of interactions
between the circulating leukocytes and the endothelial
cells. Leukocyte integrins play a pivotal role in leukocyte
adhesion to endothelial cells. During the process, the
activation of integrins by various chemoattractants,
especially chemokines, is essential for integrin-mediated
adhesion in which a signal transduced to the leukocyte
converts the functionally inactive integrin to an active
adhesive configuration. We have proposed that H-Rassensitive
activation of phosphoinositide 3 (PI 3)-kinase
and subsequent profilin-mediated actin polymerization,
can be involved in chemokine-induced integrindependent
adhesion of T cells. The present review
documents the relevance of cytoplasmic signaling and
cytoskeletal assembly to integrin-mediated adhesion
induced by chemoattractants including chemokines
during inflammatory processes. In contrast, various
adhesion molecules are known to transduce extracellular
information into cytoplasm, which leads to T cell
activation and cytokine production from the cells,
designated "outside-in signaling". Such a bi-directional
"cross-talking" among adhesion molecules and cytokines
is most relevant to inflammatory processes by
augmenting immune cell migration from circulation into
inflamed tissue such as rheumatoid arthritis, tumor
invasion, Behget's disease and atherosclerosis.
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