Spatial proteomics revealed a CX3CL1-dependent crosstalk between the urothelium and relocated macrophages through IL-6 during an acute bacterial infection in the urinary bladder
Jenny Bottek, Camille Soun, Julia K. Lill, Akanksha Dixit, Stephanie Thiebes, Anna-Lena Beerlage, Marius Horstmann, Annett Urbanek, Heike Heuer, Julian Uszkoreit, Martin Eisenacher, Thilo Bracht, Barbara Sitek, Franziska Hoffmann, Nirojah Vijitha, Ferdinand von Eggeling, Daniel R. Engel
Abstract
The urothelium of the urinary bladder represents the first line of defense. However, uropathogenic E. coli (UPEC) damage the urothelium and cause acute bacterial infection. Here, we demonstrate the crosstalk between macrophages and the urothelium stimulating macrophage migration into the urothelium. Using spatial proteomics by MALDI-MSI and LC-MS/MS, a novel algorithm revealed the spatial activation and migration of macrophages. Analysis of the spatial proteome unravelled the coexpression of Myo9b and F4/80 in the infected urothelium, indicating that macrophages have entered the urothelium upon infection. Immunofluorescence microscopy additionally indicated that intraurothelial macrophages phagocytosed UPEC and eliminated neutrophils. Further analysis of the spatial proteome by MALDI-MSI showed strong expression of IL-6 in the urothelium and local inhibition of this molecule reduced macrophage migration into the urothelium and aggravated the infection. After IL-6 inhibition, the expression of matrix metalloproteinases and chemokines, such as CX 3 CL1 was reduced in the urothelium. Accordingly, macrophage migration into the urothelium was diminished in the absence of CX 3 CL1 signaling in Cx 3 cr1 gfp/gfp mice. Conclusively, this study describes the crosstalk between the infected urothelium and macrophages through IL-6-induced CX 3 CL1 expression. Such crosstalk facilitates the relocation of macrophages into the urothelium and reduces bacterial burden in the urinary bladder.