TY - JOUR
T1 - CXCL17 is a proinflammatory chemokine and promotes neutrophil trafficking
AU - Lowry, Emily
AU - Chellappa, Rani C.
AU - Penaranda, Brigith
AU - Sawant, Kirti V.
AU - Wakamiya, Maki
AU - Garofalo, Roberto P.
AU - Rajarathnam, Krishna
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Oxford University Press on behalf of Society for Leukocyte Biology. All rights reserved.
PY - 2024/5/29
Y1 - 2024/5/29
N2 - CXCL17, a novel member of the CXC chemokine class, has been implicated in several human pathologies, but its role in mediating immune response is not well understood. Characteristic features of immune response include resident macrophages orchestrating successive and structured recruitment of neutrophils and monocytes to the insult site. Here, we show that Cxcl17 knockout (KO) mice, compared with the littermate wild-type control mice, were significantly impaired in peritoneal neutrophil recruitment post-lipopolysaccharide (LPS) challenge. Further, the KO mice show dysregulated Cxcl1, Cxcr2, and interleukin-6 levels, all of which directly impact neutrophil recruitment. Importantly, the KO mice showed no difference in monocyte recruitment post-LPS challenge or in peritoneal macrophage levels in both unchallenged and LPS-challenged mice. We conclude that Cxcl17 is a proinflammatory chemokine and that it plays an important role in the early proinflammatory response by promoting neutrophil recruitment to the insult site.
AB - CXCL17, a novel member of the CXC chemokine class, has been implicated in several human pathologies, but its role in mediating immune response is not well understood. Characteristic features of immune response include resident macrophages orchestrating successive and structured recruitment of neutrophils and monocytes to the insult site. Here, we show that Cxcl17 knockout (KO) mice, compared with the littermate wild-type control mice, were significantly impaired in peritoneal neutrophil recruitment post-lipopolysaccharide (LPS) challenge. Further, the KO mice show dysregulated Cxcl1, Cxcr2, and interleukin-6 levels, all of which directly impact neutrophil recruitment. Importantly, the KO mice showed no difference in monocyte recruitment post-LPS challenge or in peritoneal macrophage levels in both unchallenged and LPS-challenged mice. We conclude that Cxcl17 is a proinflammatory chemokine and that it plays an important role in the early proinflammatory response by promoting neutrophil recruitment to the insult site.
KW - inflammation
KW - lipopolysaccharide
KW - macrophage
KW - monocyte
KW - peritoneum
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U2 - 10.1093/jleuko/qiae028
DO - 10.1093/jleuko/qiae028
M3 - Article
C2 - 38298146
AN - SCOPUS:85194957743
SN - 0741-5400
VL - 115
SP - 1177
EP - 1182
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 6
ER -