Spatially Restricted Stromal Wnt Signaling Restrains Prostate Epithelial Progenitor Growth through Direct and Indirect Mechanisms

Spatially Restricted Stromal Wnt Signaling Restrains Prostate Epithelial Progenitor Growth through Direct and Indirect Mechanisms
Title:
Spatially Restricted Stromal Wnt Signaling Restrains Prostate Epithelial Progenitor Growth through Direct and Indirect Mechanisms
Other Titles:
Cell Stem Cell
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Publication Date:
11 April 2019
Citation:
Spatially Restricted Stromal Wnt Signaling Restrains Prostate Epithelial Progenitor Growth through Direct and Indirect Mechanisms Wei, Xing et al. Cell Stem Cell, Volume 24, Issue 5, 753 - 768.e6
Abstract:
Cell-autonomous Wnt signaling has well-characterized functions in controlling stem cell activity, including in the prostate. While niche cells secrete Wnt ligands, the effects of Wnt signaling in niche cells per se are less understood. Here, we show that stromal cells in the proximal prostatic duct near the urethra, a mouse prostate stem cell niche, not only produce multiple Wnt ligands but also exhibit strong Wnt/β-catenin activity. The non-canonical Wnt ligand Wnt5a, secreted by proximal stromal cells, directly inhibits proliefration of prostate epithelial stem or progenitor cells whereas stromal cell-autonomous canonical Wnt/β-catenin signaling indirectly suppresses prostate stem or progenitor activity via the transforming growth factor β (TGFβ) pathway. Collectively, these pathways restrain the proliferative potential of epithelial cells in the proximal prostatic ducts. Human prostate likewise exhibits spatially restricted distribution of stromal Wnt/β-catenin activity, suggesting a conserved mechanism for tissue patterning. Thus, this study shows how distinct stromal signaling mechanisms within the prostate cooperate to regulate tissue homeostasis.
License type:
PublisherCopyrights
Funding Info:
We thank the Cytometry and Cell Sorting Core at Baylor College of Medicine ( NIH AI036211 , CA125123 , and RR024574 ) for technical support and Joel M. Sederstrom for expert assistance. W.X. and B.D were supported by National Natural Science Foundation of China ( 81572536 and 81672850 ). This work was supported by NIDDK ( R01DK092202 and R01DK107436 to L.X.).
Description:
The full paper is available for download at the publisher's URL: https://doi.org/10.1016/j.stem.2019.03.010
ISSN:
1934-5909
1875-9777
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