Post-Aire Medullary Thymic Epithelial Cells and Hassall's Corpuscles as Inducers of Tonic Pro-Inflammatory Microenvironment

• Published in: Frontiers in immunology Vol. 12; p. 635569
• Main Authors: Laan, Martti, Salumets, Ahto, Klein, Annabel, Reintamm, Kerli, Bichele, Rudolf, Peterson, Hedi, Peterson, Pärt
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 02.04.2021
• Subjects: AIRE; AIRE Protein; Animals; Calgranulin A - metabolism; Calgranulin B - metabolism; Cell Differentiation; Cellular Microenvironment; Central Tolerance; Child, Preschool; Epithelial Cells - immunology; Epithelial Cells - metabolism; Hassall’s corpuscles; Humans; Immunology; Infant; Inflammation Mediators - metabolism; medullary thymic epithelial cells; Mice; Proteome; Proteomics; S100A8; thymus; Thymus Gland - immunology; Thymus Gland - metabolism; Toll-Like Receptor 4 - metabolism; Transcription Factors - metabolism; Hassall’s corpuscles; TLR4 – Toll-like receptor 4; thymus; AIRE; central tolerance; S100A9; medullary thymic epithelial cells; S100A8
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2021.635569

While there is convincing evidence on the role of Aire-positive medullary thymic epithelial cells (mTEC) in the induction of central tolerance, the nature and function of post-Aire mTECs and Hassall's corpuscles have remained enigmatic. Here we summarize the existing data on these late stages of mTEC differentiation with special focus on their potential to contribute to central tolerance induction by triggering the unique pro-inflammatory microenvironment in the thymus. In order to complement the existing evidence that has been obtained from mouse models, we performed proteomic analysis on microdissected samples from human thymic medullary areas at different differentiation stages. The analysis confirms that at the post-Aire stages, the mTECs lose their nuclei but maintain machinery required for translation and exocytosis and also upregulate proteins specific to keratinocyte differentiation and cornification. In addition, at the late stages of differentiation, the human mTECs display a distinct pro-inflammatory signature, including upregulation of the potent endogenous TLR4 agonist S100A8/S100A9. Collectively, the study suggests a novel mechanism by which the post-Aire mTECs and Hassall's corpuscles contribute to the thymic microenvironment with potential cues on the induction of central tolerance.