CXCL11型
CXCL9型
CXCL10型
趋化因子
生物
CXCR3型
免疫系统
C-C趋化因子受体6型
CXCL16型
CCR1
趋化因子受体CCR5
CCL21型
免疫学
细胞生物学
趋化因子受体
病毒学
作者
Lennard Dalit,Carolina Alvarado,Lisan H Kuijper,Andrew J. Kueh,Ashley Weir,Angela D’Amico,Marco J Herold,James E. Vince,Stephen L. Nutt,Joanna R Groom
摘要
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.
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