Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Dingding Ai
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Minea L Hoppe
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Laura T Winter
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Daniel Bohnert
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Dominik Karl
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Stefan Guenther
ECCPS Bioinformatics and Deep Sequencing Platform, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany
Slava Epelman
Ted Rogers Center of Heart Research, Peter Munk Cardiac Centre, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada
Crystal Kantores
Ted Rogers Center of Heart Research, Peter Munk Cardiac Centre, Toronto General Hospital Research Institute, University Health Network, Toronto, Canada
Monika Fijak
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Sarina Ravens
Institute of Immunology, Hannover Medical School, Hanover, Germany
Ralf Middendorff
Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany; Institute of Anatomy and Cell Biology, Unit of Signal Transduction, Justus-Liebig-University of Giessen, Giessen, Germany
Department of Dermatology and Allergology, Philipps-University of Marburg, Marburg, Germany
Kate L Loveland
Centre of Reproductive Health, Hudson Institute of Medical Research, Clayton, Australia; Department of Molecular and Translational Sciences, School of Clinical Sciences, Monash Medical Centre, Monash University, Clayton, Australia
Mark Hedger
Centre of Reproductive Health, Hudson Institute of Medical Research, Clayton, Australia; Department of Molecular and Translational Sciences, School of Clinical Sciences, Monash Medical Centre, Monash University, Clayton, Australia
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany
Andreas Meinhardt
Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig-University Giessen, Giessen, Germany; Hessian Center of Reproductive Medicine, Justus-Liebig-University of Giessen, Giessen, Germany; Centre of Reproductive Health, Hudson Institute of Medical Research, Clayton, Australia
The epididymis functions as transition zone for post-testicular sperm maturation and storage and faces contrasting immunological challenges, i.e. tolerance towards spermatozoa vs. reactivity against pathogens. Thus, normal organ function and integrity relies heavily on a tightly controlled immune balance. Previous studies described inflammation-associated tissue damage solely in the distal regions (corpus, cauda), but not in the proximal regions (initial segment, caput). To understand the observed region-specific immunity along the epididymal duct, we have used an acute bacterial epididymitis mouse model and analyzed the disease progression. Whole transcriptome analysis using RNAseq 10 days post infection showed a pro-inflammatory environment within the cauda, while the caput exhibited only minor transcriptional changes. High-dimensional flow cytometry analyses revealed drastic changes in the immune cell composition upon infection with uropathogenic Escherichia coli. A massive influx of neutrophils and monocytes was observed exclusively in distal regions and was associated with bacterial appearance and tissue alterations. In order to clarify the reasons for the region-specific differences in the intensity of immune responses, we investigated the heterogeneity of resident immune cell populations under physiological conditions by scRNASeq analysis of extravascular CD45+ cells. Twelve distinct immune cell subsets were identified, displaying substantial differences in distribution along the epididymis as further assessed by flow cytometry and immunofluorescence staining. Macrophages constituted the majority of resident immune cells and were further separated in distinct subgroups based on their transcriptional profile, tissue location and monocyte-dependence. Crucially, the proximal and distal regions showed striking differences in their immunological landscapes. These findings indicate that resident immune cells are strategically positioned along the epididymal duct, potentially providing different immunological environments required for addressing the contrasting immunological challenges and thus, preserving tissue integrity and organ function.