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Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells
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 local...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2767347/ https://www.ncbi.nlm.nih.gov/pubmed/19811645 http://dx.doi.org/10.1186/1471-213X-9-50 |
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author | Zhang, Jingxian Lipinski, Robert J Gipp, Jerry J Shaw, Aubie K Bushman, Wade |
author_facet | Zhang, Jingxian Lipinski, Robert J Gipp, Jerry J Shaw, Aubie K Bushman, Wade |
author_sort | Zhang, Jingxian |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2767347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27673472009-10-27 Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells Zhang, Jingxian Lipinski, Robert J Gipp, Jerry J Shaw, Aubie K Bushman, Wade BMC Dev Biol Research Article 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. BioMed Central 2009-10-07 /pmc/articles/PMC2767347/ /pubmed/19811645 http://dx.doi.org/10.1186/1471-213X-9-50 Text en Copyright © 2009 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Jingxian Lipinski, Robert J Gipp, Jerry J Shaw, Aubie K Bushman, Wade Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title | Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title_full | Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title_fullStr | Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title_full_unstemmed | Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title_short | Hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
title_sort | hedgehog pathway responsiveness correlates with the presence of primary cilia on prostate stromal cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2767347/ https://www.ncbi.nlm.nih.gov/pubmed/19811645 http://dx.doi.org/10.1186/1471-213X-9-50 |
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