Distinct olfactory mucosal macrophage populations mediate neuronal maintenance and pathogen defense

• Published in: Mucosal immunology Vol. 17; no. 5; pp. 1102 - 1113
• Main Authors: Wellford, Sebastian A., Chen, Ching-Wen, Vukovic, Marko, Batich, Kristen A., Lin, Elliot, Shalek, Alex K., Ordovas-Montanes, Jose, Moseman, Annie Park, Moseman, E. Ashley
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-10-2024
• ISSN: 1933-0219; 1935-3456; 1935-3456
• DOI: 10.1016/j.mucimm.2024.07.009

The olfactory mucosa is important for both the sense of smell and as a mucosal immune barrier to the upper airway and brain. However, little is known about how the immune system mediates the conflicting goals of neuronal maintenance and inflammation in this tissue. A number of immune cell populations reside within the olfactory mucosa and yet we have little understanding of how these resident olfactory immune cells functionally interact with the chemosensory environment. Identifying these interactions will allow therapeutic manipulations that treat disorders such as post-viral olfactory dysfunction. Macrophages are the most prevalent immune cell type in the uninflamed olfactory mucosa and here, we identify two distinct tissue macrophage populations in murine olfactory mucosa. P2ry12hi macrophages are transcriptionally specialized for neuron interactions, closely associated with olfactory neuron cell bodies, long-term tissue residents, and functionally specialized to phagocytose cells and debris, including olfactory neurons. Conversely, MHC Class IIhi macrophages are transcriptionally dedicated to cytokine production and antigen presentation, localized primarily within the olfactory lamina propria, more rapidly replaced by blood monocytes, and rapidly produce chemokines in response to viral infection. We further show that these macrophage signatures are present in human olfactory biopsies, and P2ry12-like olfactory macrophages are reduced in patients with long-term smell loss following COVID-19. Together, these data show that two olfactory macrophage populations regulate neurons and initiate the immune response, contributing to our understanding of both olfactory immunity and tissue-resident macrophage biology.