Bronchial epithelial cells induce alternatively activated dendritic cells dependent on glucocorticoid receptor signaling

• Published in: The Journal of immunology (1950) 2014-08, Vol.193 (3), p.1475-1484
• Main Authors: Weitnauer, Michael, Schmidt, Lotte, Ng Kuet Leong, Nathalie, Muenchau, Stephanie, Lasitschka, Felix, Eckstein, Volker, Hübner, Sabine, Tuckermann, Jan, Dalpke, Alexander H
• Format: Article
• Language: English
• Subjects: Animals; Bronchi - cytology; Bronchi - immunology; Bronchi - secretion; Cellular Microenvironment - genetics; Cellular Microenvironment - immunology; Cytokines - metabolism; Cytokines - physiology; Cytokines - secretion; Dendritic Cells - cytology; Dendritic Cells - immunology; Dendritic Cells - secretion; Female; Immunophenotyping; Inflammation - genetics; Inflammation - immunology; Inflammation - prevention & control; Mice; Mice, Inbred C57BL; Mice, Transgenic; Primary Cell Culture; Random Allocation; Receptor Cross-Talk - immunology; Receptors, Glucocorticoid - biosynthesis; Receptors, Glucocorticoid - deficiency; Receptors, Glucocorticoid - genetics; Respiratory Mucosa - cytology; Respiratory Mucosa - immunology; Respiratory Mucosa - secretion; Signal Transduction - genetics; Signal Transduction - immunology
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1400446

Airway epithelial cells mount a tolerogenic microenvironment that reduces the proinflammatory potential of respiratory dendritic cells (DCs). We recently demonstrated that tracheal epithelial cells continuously secrete soluble mediators that affect the reactivity of local innate immune cells. Using transcriptional profiling, we now observed that conditioning of DCs by tracheal epithelial cells regulated 98 genes under homeostatic conditions. Among the most upregulated genes were Ms4a8a and Ym1, marker genes of alternatively activated myeloid cells. Ex vivo analysis of respiratory DCs from nonchallenged mice confirmed a phenotype of alternative activation. Bioinformatic analysis showed an overrepresentation of hormone-nuclear receptors within the regulated genes, among which was the glucocorticoid receptor. In line with a role for glucocorticoids, pharmacological blockade as well as genetic manipulation of the glucocorticoid receptor within DCs inhibited Ms4a8a and Ym1 expression as well as MHC class II and CD86 regulation upon epithelial cell conditioning. Within epithelial cell-conditioned medium, low amounts of glucocorticoids were present. Further analysis showed that airway epithelial cells did not produce glucocorticoids de novo, yet were able to reactivate inactive dehydrocorticosterone enzymatically. The results show that airway epithelial cells regulate local immune responses, and this modulation involves local production of glucocorticoids and induction of an alternative activation phenotype in DCs.