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Lymphocytes egress from lymphoid organs in response to sphingosine-1-phosphate (S1P); minutes later they migrate from blood into tissue against the S1P gradient. The mechanisms facilitating cell movement against the gradient have not been defined. Here, we show that heterotrimeric guanine nucleotide-binding protein-coupled receptor kinase-2 (GRK2) functions in down-regulation of S1P receptor-1 (S1PR1) on blood-exposed lymphocytes. T and B cell movement from blood into lymph nodes is reduced in the absence of GRK2 but is restored in S1P-deficient mice. In the spleen, B cell movement between the blood-rich marginal zone and follicles is disrupted by GRK2 deficiency and by mutation of an S1PR1 desensitization motif. Moreover, delivery of systemic antigen into follicles is impaired. Thus, GRK2-dependent S1PR1 desensitization allows lymphocytes to escape circulatory fluids and migrate into lymphoid tissues.

Original publication

DOI

10.1126/science.1208248

Type

Journal article

Journal

Science (New York, N.Y.)

Publication Date

09/2011

Volume

333

Pages

1898 - 1903

Addresses

Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA.

Keywords

Lymph Nodes, Spleen, B-Lymphocytes, T-Lymphocytes, Blood, Animals, Mice, Inbred C57BL, Mice, Sphingosine, Lysophospholipids, Receptors, Lysosphingolipid, Chemokines, Antigen-Antibody Complex, Ligands, Signal Transduction, Cell Movement, Chemotaxis, Leukocyte, Down-Regulation, Mutation, G-Protein-Coupled Receptor Kinase 2