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Publication : Single-cell RNA sequencing reveals unique monocyte-derived interstitial macrophage subsets during lipopolysaccharide-induced acute lung inflammation.

First Author  Moore PK Year  2023
Journal  Am J Physiol Lung Cell Mol Physiol Volume  324
Issue  4 Pages  L536-L549
PubMed ID  36852927 Mgi Jnum  J:335693
Mgi Id  MGI:7439888 Doi  10.1152/ajplung.00223.2022
Citation  Moore PK, et al. (2023) Single-Cell RNA Sequencing Reveals Unique Monocyte-derived Interstitial Macrophage Subsets during Lipopolysaccharide-Induced Acute Lung Inflammation. Am J Physiol Lung Cell Mol Physiol
abstractText  Interstitial macrophages (IMs) reside in the lung tissue surrounding key structures including airways, vessels, and alveoli. Recent work has described IM heterogeneity during homeostasis, however, there are limited data on IMs during inflammation. We sought to characterize IM origin, subsets, and transcriptomic profiles during homeostasis and lipopolysaccharide (LPS) induced acute lung inflammation. During homeostasis, we used three complementary methods: spectral flow cytometry, single-cell RNA-sequencing, and gene regulatory network enrichment to demonstrate that IMs can be divided into two core subsets distinguished by surface and transcriptional expression of folate receptor beta (Folr2/FRbeta). These subsets inhabited distinct niches within the lung interstitium. Within FRbeta(+) IMs we identified a subpopulation marked by co-expression of LYVE1. During acute LPS-induced inflammation, lung IM numbers expand. Lineage tracing revealed IM expansion was due to recruitment of monocyte-derived IMs. At the peak of inflammation, recruited IMs were comprised of two unique subsets defined by expression of genes associated with interferon signaling and glycolytic pathways. As recruited IMs matured, they adopted the overall transcriptional state of FRbeta(-) resident IMs but retained expression in several origin-specific genes, such as IL-1beta. FRbeta(+) IMs were of near-pure resident origin. Taken together our data show that during LPS-induced inflammation, there are distinct populations of IMs that likely have unique functions. FRBeta(+) IMs comprise a stable, resident population, while FRbeta(-) IotaMus represent a mixed population of resident and recruited IMs.
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