A single-cell atlas of the mouse and human prostate reveals heterogeneity and conservation of epithelial progenitors

Author:

Crowley Laura12345ORCID,Cambuli Francesco12345ORCID,Aparicio Luis456,Shibata Maho12345,Robinson Brian D7,Xuan Shouhong12345ORCID,Li Weiping12345,Hibshoosh Hanina58,Loda Massimo7,Rabadan Raul456,Shen Michael M12345ORCID

Affiliation:

1. Department of Medicine, Columbia University Irving Medical Center, New York, United States

2. Department of Genetics and Development, Columbia University Irving Medical Center, New York, United States

3. Department of Urology, Columbia University Irving Medical Center, New York, United States

4. Department of Systems Biology, Columbia University Irving Medical Center, New York, United States

5. Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, United States

6. Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, United States

7. Department of Pathology and Laboratory Medicine, Weill Medical College of Cornell University, New York, United States

8. Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, United States

Abstract

Understanding the cellular constituents of the prostate is essential for identifying the cell of origin for prostate adenocarcinoma. Here, we describe a comprehensive single-cell atlas of the adult mouse prostate epithelium, which displays extensive heterogeneity. We observe distal lobe-specific luminal epithelial populations (LumA, LumD, LumL, and LumV), a proximally enriched luminal population (LumP) that is not lobe-specific, and a periurethral population (PrU) that shares both basal and luminal features. Functional analyses suggest that LumP and PrU cells have multipotent progenitor activity in organoid formation and tissue reconstitution assays. Furthermore, we show that mouse distal and proximal luminal cells are most similar to human acinar and ductal populations, that a PrU-like population is conserved between species, and that the mouse lateral prostate is most similar to the human peripheral zone. Our findings elucidate new prostate epithelial progenitors, and help resolve long-standing questions about anatomical relationships between the mouse and human prostate.

Funder

National Cancer Institute

T.J. Martell Foundation

U.S. Department of Defense

National Science Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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