Skip to main content
. 2021 Aug 11;11:16348. doi: 10.1038/s41598-021-94855-5

Figure 2.

Figure 2

Generation of spontaneous inflammation in 8-month-old transgenic (TG) mice. (a) mRNA levels of cytokines (IFN-α, TNF-α, IL-17 and IFN-γ) in the spleens of 5- and 8-month-old WT and TG mice measured by qRT-PCR. (b) Flow cytometric analysis of single cells from the spleens of 8-month-old mice. ((b), upper) A strategy to determine the population of monocytes, neutrophils, macrophages and dendritic cells is represented. To investigate the population of monocytes and neutrophils, CD11b+ cells were gated first. Ly6C+Ly6G+ cells were considered to be neutrophils, and Ly6C+Ly6G- cells were considered to be monocytes. CD11b+F4/80+ cells served as macrophages, and CD11c+ cells represented neutrophils. ((b), lower) Monocyte, neutrophil, macrophage and dendritic cell populations are represented. (c) mRNA levels of cytokines IFN-α, TNF-α, IL-17 and IFN-γ, (d) mRNA expression levels of chemokines CCL2, CCL7, CCL12, CXCL1 and CX3CL1. (e) TLR7 mRNA expression levels in the kidneys of 8-month-old WT and TG mice, measured by qRT-PCR. WT, wild type. *p < 0.05; **p < 0.01, ***p < 0.001 versus WT group of the same age.