» Articles » PMID: 33208946

A Molecular Cell Atlas of the Human Lung from Single-cell RNA Sequencing

Abstract

Although single-cell RNA sequencing studies have begun to provide compendia of cell expression profiles, it has been difficult to systematically identify and localize all molecular cell types in individual organs to create a full molecular cell atlas. Here, using droplet- and plate-based single-cell RNA sequencing of approximately 75,000 human cells across all lung tissue compartments and circulating blood, combined with a multi-pronged cell annotation approach, we create an extensive cell atlas of the human lung. We define the gene expression profiles and anatomical locations of 58 cell populations in the human lung, including 41 out of 45 previously known cell types and 14 previously unknown ones. This comprehensive molecular atlas identifies the biochemical functions of lung cells and the transcription factors and markers for making and monitoring them; defines the cell targets of circulating hormones and predicts local signalling interactions and immune cell homing; and identifies cell types that are directly affected by lung disease genes and respiratory viruses. By comparing human and mouse data, we identified 17 molecular cell types that have been gained or lost during lung evolution and others with substantially altered expression profiles, revealing extensive plasticity of cell types and cell-type-specific gene expression during organ evolution including expression switches between cell types. This atlas provides the molecular foundation for investigating how lung cell identities, functions and interactions are achieved in development and tissue engineering and altered in disease and evolution.

Citing Articles

LungGENIE: the lung gene-expression and network imputation engine.

Ghosh A, Coyne L, Panda S, Menon A, Moll M, Archer M BMC Genomics. 2025; 26(1):227.

PMID: 40065206 PMC: 11892309. DOI: 10.1186/s12864-025-11412-4.


Integrated histopathology, spatial and single cell transcriptomics resolve cellular drivers of early and late alveolar damage in COVID-19.

Lee J, Barnett S, Roberts K, Ashwin H, Milross L, Cho J Nat Commun. 2025; 16(1):1979.

PMID: 40064844 PMC: 11893906. DOI: 10.1038/s41467-025-56473-x.


Investigation of cell development and tissue structure network based on natural Language processing of scRNA-seq data.

Wei S, Lu Y, Wang P, Li Q, Shuai J, Zhao Q J Transl Med. 2025; 23(1):264.

PMID: 40038714 PMC: 11877821. DOI: 10.1186/s12967-025-06263-2.


Heparan sulfate regulates amphiregulin programming of tissue reparative lung mesenchymal cells during influenza A virus infection in mice.

Loffredo L, Kustagi A, Ringham O, Li F, de Los Santos-Alexis K, Saqi A Nat Commun. 2025; 16(1):2129.

PMID: 40032825 PMC: 11876457. DOI: 10.1038/s41467-025-57362-z.


GSDMD-mediated pyroptosis: molecular mechanisms, diseases and therapeutic targets.

Li Y, Guo B Mol Biomed. 2025; 6(1):11.

PMID: 39994107 PMC: 11850691. DOI: 10.1186/s43556-025-00249-8.


References
1.
Zeisel A, Hochgerner H, Lonnerberg P, Johnsson A, Memic F, van der Zwan J . Molecular Architecture of the Mouse Nervous System. Cell. 2018; 174(4):999-1014.e22. PMC: 6086934. DOI: 10.1016/j.cell.2018.06.021. View

2.
Young J . Malpighi's "De Pulmonibus". Proc R Soc Med. 2009; 23(1):1-11. PMC: 2181528. View

3.
Muzumdar M, Tasic B, Miyamichi K, Li L, Luo L . A global double-fluorescent Cre reporter mouse. Genesis. 2007; 45(9):593-605. DOI: 10.1002/dvg.20335. View

4.
Butler A, Hoffman P, Smibert P, Papalexi E, Satija R . Integrating single-cell transcriptomic data across different conditions, technologies, and species. Nat Biotechnol. 2018; 36(5):411-420. PMC: 6700744. DOI: 10.1038/nbt.4096. View

5.
van Amerongen R, Bowman A, Nusse R . Developmental stage and time dictate the fate of Wnt/β-catenin-responsive stem cells in the mammary gland. Cell Stem Cell. 2012; 11(3):387-400. DOI: 10.1016/j.stem.2012.05.023. View