Background. Hedgehog (Hh) signaling from the urogenital sinus (UGS) epithelium to the surrounding mesenchyme plays a critical role in regulating ductal formation and growth during prostate development. The primary cilium, a feature of most interphase vertebrate cell types, serves as a required localization domain for Hh signaling transducing proteins. Results. Immunostaining revealed the presence of primary cilia in mesenchymal cells of the developing prostate. Cell-based assays of a urongenital sinus mesenchymal cell line (UGSM-2) revealed that proliferation-limiting (serum starvation and/or confluence) growth conditions promoted cilia formation and correlated with pathway activation associated with accumulation of Smoothened in primary cilia. The prostate cancer cell lines PC-3, LNCaP, and 22RV1, previously shown to lack demonstrable autocrine Hh signaling capacity, did not exhibit primary cilia even under proliferation-limiting growth conditions. Conclusion. We conclude that paracrine Hedgehog signaling activity in the prostate is associated with the presence of primary cilia on stromal cells but that a role in autocrine Hh signaling remains speculative.
|Original language||English (US)|
|Journal||BMC Developmental Biology|
|State||Published - 2009|
Bibliographical noteFunding Information:
The authors would like to Kathleen Sulik, Deborah Dehart, Crist Cook and Kathy Schell and the UW-CCC Flow Cytometry facility for technical assistance. This work was supported from the National Institute of Health (DK065303-01 and DK056238) and the Robert and Delores Schnoes Chair in Urologic Research.