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The sphingosine 1-phosphate receptor 1 causes tissue retention by inhibiting the entry of peripheral tissue T lymphocytes into afferent lymphatics.
Ledgerwood, Levi G; Lal, Girdhari; Zhang, Nan; Garin, Alexandre; Esses, Steven J; Ginhoux, Florent; Merad, Miriam; Peche, Helene; Lira, Sergio A; Ding, Yaozhong; Yang, Yu; He, Xingxuan; Schuchman, Edward H; Allende, Maria L; Ochando, Jordi C; Bromberg, Jonathan S.
Afiliação
  • Ledgerwood LG; Department of Gene and Cell Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.
Nat Immunol ; 9(1): 42-53, 2008 Jan.
Article em En | MEDLINE | ID: mdl-18037890
ABSTRACT
Although much is known about the migration of T cells from blood to lymph nodes, less is known about the mechanisms regulating the migration of T cells from tissues into lymph nodes through afferent lymphatics. Here we investigated T cell egress from nonlymphoid tissues into afferent lymph in vivo and developed an experimental model to recapitulate this process in vitro. Agonism of sphingosine 1-phosphate receptor 1 inhibited the entry of tissue T cells into afferent lymphatics in homeostatic and inflammatory conditions and caused the arrest, mediated at least partially by interactions of the integrin LFA-1 with its ligand ICAM-1 and of the integrin VLA-4 with its ligand VCAM-1, of polarized T cells at the basal surface of lymphatic but not blood vessel endothelium. Thus, the increased sphingosine 1-phosphate present in inflamed peripheral tissues may induce T cell retention and suppress T cell egress.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esfingosina / Lisofosfolipídeos / Linfócitos T / Modelos Imunológicos / Vasos Linfáticos / Receptores de Lisoesfingolipídeo Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2008 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esfingosina / Lisofosfolipídeos / Linfócitos T / Modelos Imunológicos / Vasos Linfáticos / Receptores de Lisoesfingolipídeo Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2008 Tipo de documento: Article