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Autocrine Secretion of Interferon γ Negatively Regulates Homing of Immature B Cells

The mechanism by which immature B cells are sequestered from encountering foreign antigens present in lymph nodes or sites of inflammation, before their final maturation in the spleen, has not been elucidated. We show here that immature B cells fail to home to the lymph nodes. These cells can active...

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Detalles Bibliográficos
Autores principales: Flaishon, Liat, Hershkoviz, Rami, Lantner, Frida, Lider, Ofer, Alon, Ronen, Levo, Yoram, Flavell, Richard A., Shachar, Idit
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193359/
https://www.ncbi.nlm.nih.gov/pubmed/11067886
Descripción
Sumario:The mechanism by which immature B cells are sequestered from encountering foreign antigens present in lymph nodes or sites of inflammation, before their final maturation in the spleen, has not been elucidated. We show here that immature B cells fail to home to the lymph nodes. These cells can actively exclude themselves from antigen-enriched sites by downregulating their integrin-mediated adhesion to the extracellular matrix protein, fibronectin. This inhibition is mediated by interferon γ secretion. Perturbation of interferon γ activity in vivo leads to the homing of immature B cells to the lymph nodes. This is the first example of autocrine regulation of immune cell migration to sites of foreign antigen presentation.