Spatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage niches.

ABSTRACT: The liver is the largest solid organ in the body, yet it remains incompletely characterized. Here we present a spatial proteogenomic atlas of the healthy and obese human and murine liver combining single-cell CITE-seq, single-nuclei sequencing, spatial transcriptomics, and spatial proteomics. By integrating these multi-omic datasets, we provide validated strategies to reliably discriminate and localize all hepatic cells, including a population of lipid-associated macrophages (LAMs) at the bile ducts. We then align this atlas across seven species, revealing the conserved program of bona fide Kupffer cells and LAMs. We also uncover the respective spatially resolved cellular niches of these macrophages and the microenvironmental circuits driving their unique transcriptomic identities. We demo

SUBMITTER: Guilliams M 

PROVIDER: S-EPMC8809252 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature