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Cortical sinus probing, S1P(1)-dependent entry and flow-based capture of egressing T cells

The cellular dynamics of lymphocyte egress from lymph nodes are poorly defined. Here, we visualized the branched organization of lymph node cortical sinuses and found that after entry some T cells were retained while others returned to the parenchyma. Sphingosine-1-phosphate receptor 1 (S1P(1))-defi...

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Detalles Bibliográficos
Autores principales: Grigorova, Irina L, Schwab, Susan R, Phan, Tri Giang, Pham, Trung H M, Okada, Takaharu, Cyster, Jason G
Formato: Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2710451/
https://www.ncbi.nlm.nih.gov/pubmed/19060900
http://dx.doi.org/10.1038/ni.1682
Descripción
Sumario:The cellular dynamics of lymphocyte egress from lymph nodes are poorly defined. Here, we visualized the branched organization of lymph node cortical sinuses and found that after entry some T cells were retained while others returned to the parenchyma. Sphingosine-1-phosphate receptor 1 (S1P(1))-deficient T cells probed the sinus surface but failed to enter. In some sinuses T cells became rounded and moved in a unidirectional fashion. T cells traveled from cortical sinuses into macrophage-rich sinus areas. Many T cells flowed from medullary sinuses into the subcapsular space. We propose a multistep model of lymph node egress where cortical sinus probing is followed by S1P(1)-dependent entry, capture of cells in a sinus region with flow and transport to medullary sinuses and the efferent lymph.