Publication Date:
1998-02-07
Description:
Circulating lymphocytes are recruited from the blood to the tissue by rolling along the endothelium until being stopped by a signaling event linked to the Gialpha subunit of a heterotrimeric GTP-binding protein; that event then triggers rapid integrin-dependent adhesion. Four chemokines are now shown to induce such adhesion to intercellular adhesion molecule-1 and to induce arrest of rolling cells within 1 second under flow conditions similar to those of blood. SDF-1 (also called PBSF), 6-C-kine (also called Exodus-2), and MIP-3beta (also called ELC or Exodus-3) induced adhesion of most circulating lymphocytes, including most CD4+ T cells; and MIP-3alpha (also called LARC or Exodus-1) triggered adhesion of memory, but not naive, CD4+ T cells. Thus, chemokines can regulate the arrest of lymphocyte subsets under flowing conditions, which may allow them to control lymphocyte-endothelial cell recognition and lymphocyte recruitment in vivo.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Campbell, J J -- Hedrick, J -- Zlotnik, A -- Siani, M A -- Thompson, D A -- Butcher, E C -- 5T32CA090302/CA/NCI NIH HHS/ -- DK38707/DK/NIDDK NIH HHS/ -- GM37734/GM/NIGMS NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1998 Jan 16;279(5349):381-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Immunology and Vascular Biology, Department of Pathology, and Digestive Disease Center, Department of Medicine, Stanford University Medical School, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9430588" target="_blank"〉PubMed〈/a〉
Keywords:
Antigens, Surface/metabolism
;
CD4-Positive T-Lymphocytes/*physiology
;
*Cell Adhesion
;
Chemokine CCL19
;
Chemokine CCL20
;
Chemokine CCL21
;
Chemokine CXCL12
;
Chemokines, CC/*pharmacology/physiology
;
*Chemokines, CXC
;
Humans
;
Immunologic Memory
;
Intercellular Adhesion Molecule-1/metabolism
;
Lymphocytes/*physiology
;
*Macrophage Inflammatory Proteins
;
Membrane Proteins
;
Receptors, CCR6
;
*Receptors, Chemokine
;
Rheology
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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