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Genetic background affects neutrophil activity and determines the severity of autoinflammatory osteomyelitis in mice

. 2024 Dec 31 ; 117 (1) : .

Language English Country Great Britain, England Media print

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
378521 Grant Agency of Charles University
23-06676S Czech Science Foundation
RVO 68378050 Institute of Molecular Genetics of the Czech Academy of Sciences
LX22NPO5102 National Institute for Cancer Research
European Union-Next Generation EU
Czech Centre for Phenogenomics
LM2023036 Ministry of Education, Youth and Sports of the Czech Republic
CZ.02.1.01/0.0/0.0/18_046/0015861 CCP Infrastructure Upgrade II
European Structural and Investment Funds

The knowledge about the contribution of the innate immune system to health and disease is expanding. However, to obtain reliable results, it is critical to select appropriate mouse models for in vivo studies. Data on genetic and phenotypic changes associated with different mouse strains can assist in this task. Such data can also facilitate our understanding of how specific polymorphisms and genetic alterations affect gene function, phenotypes, and disease outcomes. Extensive information is available on genetic changes in all major mouse strains. However, comparatively little is known about their impact on immune response and, in particular, on innate immunity. Here, we analyzed a mouse model of chronic multifocal osteomyelitis, an autoinflammatory disease driven exclusively by the innate immune system, which is caused by an inactivating mutation in the Pstpip2 gene. We investigated how the genetic background of BALB/c, C57BL/6J, and C57BL/6NCrl strains alters the molecular mechanisms controlling disease progression. While all mice developed the disease, symptoms were significantly milder in BALB/c and partially also in C57BL/6J when compared to C57BL/6NCrl. Disease severity correlated with the number of infiltrating neutrophils and monocytes and with the production of chemokines attracting these cells to the site of inflammation. It also correlated with increased expression of genes associated with autoinflammation, rheumatoid arthritis, neutrophil activation, and degranulation, resulting in altered neutrophil activation in vivo. Together, our data demonstrate striking effects of genetic background on multiple parameters of neutrophil function and activity influencing the onset and course of chronic multifocal osteomyelitis.

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