Back to Search Start Over

CXCL11 expressing C57BL/6 mice have intact adaptive immune responses to viral infection

Authors :
Dalit, L
Alvarado, C
Kuijper, L
Kueh, AJ
Weir, A
D'Amico, A
Herold, MJ
Vince, JE
Nutt, SL
Groom, JR
Dalit, L
Alvarado, C
Kuijper, L
Kueh, AJ
Weir, A
D'Amico, A
Herold, MJ
Vince, JE
Nutt, SL
Groom, JR
Publication Year :
2022

Abstract

The chemokine receptor CXCR3 is expressed on immune cells to co-ordinate lymphocyte activation and migration. CXCR3 binds three chemokine ligands, CXCL9, CXCL10 and CXCL11. These ligands display distinct expression patterns and ligand signaling biases; however, how each ligand functions individually and collaboratively is incompletely understood. CXCL9 and CXCL10 are considered pro-inflammatory chemokines during viral infection, while CXCL11 may induce a tolerizing state. The investigation of the individual role of CXCL11 in vivo has been hampered as C57BL/6 mice carry several mutations that result in a null allele. Here, CRISPR/Cas9 was used to correct these mutations on a C57BL/6 background. It was validated that CXCL11KI mice expressed CXCL11 protein in dendritic cells, spleen and lung. CXCL11KI mice were largely phenotypically indistinguishable from C57BL/6 mice, both at steady-state and during two models of viral infection. While CXCL11 expression did not modify acute antiviral responses, this study provides a new tool to understand the role of CXCL11 in other experimental settings.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1340014644
Document Type :
Electronic Resource