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Publication : Intrasplenic trafficking of natural killer cells is redirected by chemokines upon inflammation.

First Author  Grégoire C Year  2008
Journal  Eur J Immunol Volume  38
Issue  8 Pages  2076-84
PubMed ID  18624307 Mgi Jnum  J:138561
Mgi Id  MGI:3805408 Doi  10.1002/eji.200838550
Citation  Gregoire C, et al. (2008) Intrasplenic trafficking of natural killer cells is redirected by chemokines upon inflammation. Eur J Immunol 38(8):2076-84
abstractText  The spleen is a major homing site for NK cells. How they traffic to and within this site in homeostatic or inflammatory conditions is, however, mostly unknown. Here we show that NK cells enter the spleen through the marginal sinus and home to the red pulp via a pertussis toxin-insensitive mechanism. Upon inflammation induced by poly(I:C) injection or mouse cytomegalovirus infection, many NK cells left the red pulp while others transiently entered the white pulp, predominantly the T cell area. This migration was dependent on both CXCR3 and CCL5, suggesting a synergy between CXCR3 and CCR5, and followed the path lined by fibroblastic reticular cells. Thus, the entry of NK cells in the white pulp is limited by the expression of pro-inflammatory chemokines. This phenomenon ensures the segregation of NK cells outside of the white pulp and might contribute to the control of immunopathology.
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