4.8 Article

Expansion of Luminal Progenitor Cells in the Aging Mouse and Human Prostate

Journal

CELL REPORTS
Volume 28, Issue 6, Pages 1499-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.07.007

Keywords

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Funding

  1. NIH [P30 CA016042, 5P30 AI028697]
  2. James B. Pendleton Charitable Trust
  3. UCLA Minor in Biomedical Research
  4. Silva Endowment as part of the Undergraduate Research Scholars Program at UCLA
  5. Ruth L. Kirschstein National Research Service Award [GM007185]
  6. Eugene V. Cota-Robles Fellowship
  7. National Institute of General Medical Sciences of the NIH [R25GM055052]
  8. Saul Martinez Scholarship
  9. Spitzer Family Foundation Fund
  10. Gill Endowment
  11. American Cancer Society [RSG-17-068-01-TBG]
  12. Department of Defense [W81XWH-13-1-0470]
  13. Margaret E. Early Medical Research Trust
  14. STOP CANCER [P50CA092131/UCLA]
  15. UCLA Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research Rose Hills Foundation Innovator Grant
  16. UCLA's Jonsson Comprehensive Cancer Center, Broad Stem Cell Research Center, Clinical and Translational Science Institute
  17. Institute of Urologic Oncology
  18. NIH/NIDDK [R01 DK115477]
  19. UCLA's Technology Center for Genomics and Bioinformatics, Translational Pathology Core Laboratories
  20. UCLA's Institute for Quantitative and Computational Biology

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Aging is associated with loss of tissue mass and a decline in adult stem cell function in many tissues. In contrast, aging in the prostate is associated with growth-related diseases including benign prostatic hyperplasia (BPH). Surprisingly, the effects of aging on prostate epithelial cells have not been established. Here we find that organoid-forming progenitor activity of mouse prostate basal and luminal cells is maintained with age. This is caused by an agerelated expansion of progenitor-like luminal cells that share features with human prostate luminal progenitor cells. The increase in luminal progenitor cells may contribute to greater risk for growth-related disease in the aging prostate. Importantly, we demonstrate expansion of human luminal progenitor cells in BPH. In summary, we define a Trop2(+) luminal progenitor subset and identify an age-related shift in the luminal compartment of the mouse and human prostate epithelium.

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