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Region-specific transcriptomic and functional signatures of mononuclear phagocytes in the epididymis.
- Source :
-
Molecular human reproduction [Mol Hum Reprod] 2020 Jan 01; Vol. 26 (1), pp. 14-29. - Publication Year :
- 2020
-
Abstract
- In the epididymis, prevention of autoimmune responses against spermatozoa and simultaneous protection against pathogens is important for male fertility. We have previously shown that mononuclear phagocytes (MPs) are located either in the epididymal interstitium or in close proximity to the epithelium. In the initial segments (IS), these 'intraepithelial' MPs extend slender luminal-reaching projections between epithelial cells. In this study, we performed an in-depth characterisation of MPs isolated from IS, caput-corpus and cauda epididymis of CX3CR1EGFP+/- mice that express EGFP in these cells. Flow cytometry analysis revealed region-specific subsets of MPs that express combinations of markers traditionally described in 'dendritic cells' or 'macrophages'. RNA sequencing identified distinct transcriptomic signatures in MPs from each region and revealed specific genes involved in inflammatory and anti-inflammatory responses, phagosomal activity and antigen processing and presentation. Functional fluorescent in vivo labelling assays showed that higher percentages of CX3CR1+ MPs that captured and processed antigens were detected in the IS compared to other regions. Confocal microscopy showed that in the IS, caput and corpus, circulatory antigens were internalised and processed by interstitial and intraepithelial MPs. However, in the cauda only interstitial MPs internalised and processed antigens, while intraepithelial MPs did not take up antigens, indicating that all antigens have been captured before they reached the epithelial lining. Cauda MPs may thus confer a stronger protection against blood-borne pathogens compared to proximal regions. By identifying immunoregulatory mechanisms in the epididymis, our study may lead to new therapies for male infertility and epididymitis and identify potential targets for immunocontraception.<br /> (© The Author(s) 2020. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.)
- Subjects :
- Animals
Antigen Presentation
Antigens, CD genetics
Antigens, CD immunology
Autoantigens genetics
Autoantigens immunology
CX3C Chemokine Receptor 1 deficiency
CX3C Chemokine Receptor 1 genetics
Cell Communication
Chemokines, CC genetics
Chemokines, CC immunology
Dendritic Cells cytology
Dendritic Cells immunology
Dendritic Cells metabolism
Epididymis cytology
Epididymis metabolism
Epithelial Cells cytology
Epithelial Cells immunology
Epithelial Cells metabolism
Gene Expression Profiling
Gene Expression Regulation
Green Fluorescent Proteins genetics
Green Fluorescent Proteins immunology
Male
Mice
Mice, Knockout
Phagocytes cytology
Phagocytes metabolism
Protein Transport
Receptors, Interleukin genetics
Receptors, Interleukin immunology
Receptors, Tumor Necrosis Factor, Type I genetics
Receptors, Tumor Necrosis Factor, Type I immunology
Recombinant Fusion Proteins genetics
Recombinant Fusion Proteins immunology
Spermatozoa cytology
Spermatozoa metabolism
CX3C Chemokine Receptor 1 immunology
Epididymis immunology
Fertility genetics
Phagocytes immunology
Spermatozoa immunology
Transcriptome immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2407
- Volume :
- 26
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular human reproduction
- Publication Type :
- Academic Journal
- Accession number :
- 31778536
- Full Text :
- https://doi.org/10.1093/molehr/gaz059