| Literature DB >> 31604275 |
Benjamin J Stewart1,2,3, John R Ferdinand1, Matthew D Young3, Thomas J Mitchell2,3,4, Kevin W Loudon1,2, Alexandra M Riding1,2, Nathan Richoz1, Gordon L Frazer1, Joy U L Staniforth1, Felipe A Vieira Braga3, Rachel A Botting5, Dorin-Mirel Popescu5, Roser Vento-Tormo3, Emily Stephenson5, Alex Cagan3, Sarah J Farndon3,6,7, Krzysztof Polanski3, Mirjana Efremova3, Kile Green5, Martin Del Castillo Velasco-Herrera3, Charlotte Guzzo3, Grace Collord2,3,8, Lira Mamanova3, Tevita Aho2, James N Armitage2, Antony C P Riddick2, Imran Mushtaq6, Stephen Farrell2, Dyanne Rampling6, James Nicholson2,8, Andrew Filby5, Johanna Burge2, Steven Lisgo9, Susan Lindsay9, Marc Bajenoff10, Anne Y Warren2, Grant D Stewart2,4, Neil Sebire6,7, Nicholas Coleman2,11, Muzlifah Haniffa3,5,12, Sarah A Teichmann13,14, Sam Behjati2,3,8, Menna R Clatworthy1,2,3.
Abstract
Tissue-resident immune cells are important for organ homeostasis and defense. The epithelium may contribute to these functions directly or by cross-talk with immune cells. We used single-cell RNA sequencing to resolve the spatiotemporal immune topology of the human kidney. We reveal anatomically defined expression patterns of immune genes within the epithelial compartment, with antimicrobial peptide transcripts evident in pelvic epithelium in the mature, but not fetal, kidney. A network of tissue-resident myeloid and lymphoid immune cells was evident in both fetal and mature kidney, with postnatal acquisition of transcriptional programs that promote infection-defense capabilities. Epithelial-immune cross-talk orchestrated localization of antibacterial macrophages and neutrophils to the regions of the kidney most susceptible to infection. Overall, our study provides a global overview of how the immune landscape of the human kidney is zonated to counter the dominant immunological challenge.Entities:
Mesh:
Year: 2019 PMID: 31604275 PMCID: PMC7343525 DOI: 10.1126/science.aat5031
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728