The Kidney Contains Ontogenetically Distinct Dendritic Cell and Macrophage Subtypes throughout Development That Differ in Their Inflammatory Properties

Natallia Salei, Stephan Rambichler, Johanna Salvermoser, Nikos E Papaioannou, Ronja Schuchert, Dalia Pakalniškytė, Na Li, Julian A Marschner, Julia Lichtnekert, Christopher Stremmel, Filippo M Cernilogar, Melanie Salvermoser, Barbara Walzog, Tobias Straub, Gunnar Schotta, Hans-Joachim Anders, Christian Schulz, Barbara U Schraml
Journal of the American Society of Nephrology: JASN 2020, 31 (2): 257-278

BACKGROUND: Mononuclear phagocytes (MPs), including macrophages, monocytes, and dendritic cells (DCs), are phagocytic cells with important roles in immunity. The developmental origin of kidney DCs has been highly debated because of the large phenotypic overlap between macrophages and DCs in this tissue.

METHODS: We used fate mapping, RNA sequencing, flow cytometry, confocal microscopy, and histo-cytometry to assess the origin and phenotypic and functional properties of renal DCs in healthy kidney and of DCs after cisplatin and ischemia reperfusion-induced kidney injury.

RESULTS: Adult kidney contains at least four subsets of MPs with prominent Clec9a -expression history indicating a DC origin. We demonstrate that these populations are phenotypically, functionally, and transcriptionally distinct from each other. We also show these kidney MPs exhibit unique age-dependent developmental heterogeneity. Kidneys from newborn mice contain a prominent population of embryonic-derived MHCIIneg F4/80hi CD11blow macrophages that express T cell Ig and mucin domain containing 4 (TIM-4) and MER receptor tyrosine kinase (MERTK). These macrophages are replaced within a few weeks after birth by phenotypically similar cells that express MHCII but lack TIM-4 and MERTK. MHCII+ F4/80hi cells exhibit prominent Clec9a- expression history in adulthood but not early life, indicating additional age-dependent developmental heterogeneity. In AKI, MHCIIneg F4/80hi cells reappear in adult kidneys as a result of MHCII downregulation by resident MHCII+ F4/80hi cells, possibly in response to prostaglandin E2 (PGE2). RNA sequencing further suggests MHCII+ F4/80hi cells help coordinate the recruitment of inflammatory cells during renal injury.

CONCLUSIONS: Distinct developmental programs contribute to renal DC and macrophage populations throughout life, which could have important implications for therapies targeting these cells.

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