Single-Cell RNA Sequencing Reveals the Interaction of Injected ADSCs with Lung-Originated Cells in Mouse Pulmonary Fibrosis.

Stem Cells Int

MOE Key Laboratory of Bioinformatics, Center for Synthetic and System Biology, Tsinghua University, Beijing 100084, China.

Published: April 2022

AI Article Synopsis

  • * In a study using a bleomycin-induced PF mouse model, researchers injected GFP-labeled ADSCs to analyze their interaction with lung cells at a single-cell level through RNA sequencing.
  • * The results revealed that ADSCs altered the lung cell composition, particularly increasing anti-inflammatory macrophages, which may help reduce inflammation and fibrosis, providing insights for improving ADSC therapies in PF.

Article Abstract

Pulmonary fibrosis (PF) is a severe chronic lung disease with little effective treatment options other than lung transplantation. Adipose-derived mesenchymal stem cells (ADSCs) have been shown to exert therapeutic effects on PF, but the underlying mechanisms remain to be further elucidated. Here, we show the interaction of ADSCs and lung-originated cells at the single-cell level, using bleomycin- (BLM-) induced mice PF model and green fluorescent protein- (GFP-) labeled mouse ADSCs. The intratracheally injected ADSCs were successfully recollected with flow cytometry and, together with lung-originated cells, were subjected to single-cell RNA sequencing (scRNA-seq). The ADSC treatment drastically changed the transcriptomic profile and composition of lung cells, especially macrophages. We explored the signal pathway interactions between ADSCs and lung-originated cells, showing potentially regulative pathways including NGR, ANNEXIN, HGF, and PERIOSTIN. Our data indicate that the injected ADSCs increased the number of antiinflammatory lung macrophages and lowered further inflammation and fibrosis in the lung. Our work realized the direct analysis of injected ADSCs to explore its interaction with the lung environment under PF and may provide critical information for future engineering of ADSCs to achieve better therapeutic effects in PF.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017459PMC
http://dx.doi.org/10.1155/2022/9483166DOI Listing

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