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      Urethral luminal epithelia are castration‐insensitive cells of the proximal prostate

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          Abstract

          Castration-insensitive epithelial progenitors capable of regenerating the prostate have been proposed to be concentrated in the proximal region based on facultative assays. Functional characterization of prostate epithelial populations isolated with individual cell surface markers has failed to provide a consensus on the anatomical and transcriptional identity of proximal prostate progenitors. Here, we use single-cell RNA sequencing to obtain a complete transcriptomic profile of all epithelial cells in the mouse prostate and urethra to objectively identify cellular subtypes. Pan-transcriptomic comparison to human prostate cell types identified a mouse equivalent of human urethral luminal cells, which highly expressed putative prostate progenitor markers. Validation of the urethral luminal cell cluster was performed using immunostaining and flow cytometry. Our data reveal that previously identified facultative progenitors marked by Trop2, Sca-1, KRT4, and PSCA are actually luminal epithelial cells of the urethra that extend into the proximal region of the prostate, and are resistant to castration-induced androgen deprivation. Mouse urethral luminal cells were identified to be the equivalent of previously identified human club and hillock cells that similarly extend into proximal prostate ducts. Benign prostatic hyperplasia (BPH) has long been considered an “embryonic reawakening,” but the cellular origin of the hyperplastic growth concentrated in the periurethral region is unclear. We demonstrate an increase in urethral luminal cells within glandular nodules from BPH patients. Urethral luminal cells are further increased in patients treated with a 5-α reductase inhibitor. Our data demonstrate that cells of the proximal prostate that express putative progenitor markers, and are enriched by castration in the proximal prostate, are urethral luminal cells and that these cells may play an important role in the etiology of human BPH.

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          Most cited references2

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          Origin and evolution of benign prostatic enlargement

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            Benign Prostatic Hyperplasia

            Isaacs JT (1985)
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              Author and article information

              Contributors
              (View ORCID Profile)
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              Journal
              The Prostate
              Prostate
              Wiley
              0270-4137
              1097-0045
              August 2020
              June 04 2020
              August 2020
              : 80
              : 11
              : 872-884
              Affiliations
              [1 ]Department of UrologyUT Southwestern Medical CenterDallas Texas
              [2 ]Department of BioinformaticsUT Southwestern Medical CenterDallas Texas
              [3 ]Department of Comparative Biosciences, School of Veterinary MedicineUniversity of Wisconsin‐MadisonMadison Wisconsin
              [4 ]Southwest Transplant AllianceDallas Texas
              Article
              10.1002/pros.24020
              7339731
              32497356
              5dfbb257-d038-4f13-9865-3b83f77237fd
              © 2020

              http://onlinelibrary.wiley.com/termsAndConditions#vor

              http://doi.wiley.com/10.1002/tdm_license_1.1

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