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

C Grégoire, C Cognet, L Chasson… - European journal of …, 2008 - Wiley Online Library
C Grégoire, C Cognet, L Chasson, CA Coupet, M Dalod, A Reboldi, J Marvel, F Sallusto
European journal of immunology, 2008Wiley Online Library
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 …
Abstract
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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