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Identification of stem cells that contribute to prostate development

Date:
October 15, 2012
Source:
Libre de Bruxelles, Université
Summary:
Researchers have identified multipotent and unipotent stem cells (SCs) that contribute to prostate postnatal development.

Researchers at the Université Libre de Bruxelles, ULB have identified multipotent and unipotent stem cells (SCs) that contribute to prostate postnatal development.

One of the key questions in biology is the identification of stem cells responsible for tissue morphogenesis and regeneration.

In a study published in Nature Cell Biology, researchers lead by Cédric Blanpain, MD/PhD, Welbio investigator and Professor at the Université Libre de Bruxelles, Belgium, identify novel classes of prostate SCs that ensure the development of the different cell lineages of the prostate.

The prostate is a secretory gland surrounding the urethra at the base of the bladder producing the seminal fluid providing nutrients, ions and enzymes necessary for the survival of the spermatozoids during their journey through the female reproductive tract. The adult prostate is composed of three cell lineages: the basal cells, the luminal cells and the neuroendocrine cells.

To precisely define the cellular hierarchy of the prostate during the development under physiological conditions, Marielle Ousset and colleagues used state of the art genetic lineage tracing approach to fluorescently mark the different cell types of the prostate and follow the fate of marked cells overtime. The researchers found that multipotent and unipotent SCs contribute to prostate postnatal development.

"We were very surprised and excited when we discovered that multipotent SCs ensure the major epithelial expansion, giving rise to unipotent progenitors and to neuroendocrine cells. Indeed, these results contrast to the situation we have recently found in the mammary gland, which develops through the presence of unipotent stem cells" said Marielle Ousset, PhD and co-first author of this study.

"These new findings establish a new paradigm for the mode of development of glandular epithelia and will be extremely important for those studying development, stem cells and prostate but also open new avenues to uncover the cells at the origin of the prostate cancer, a very important question, not yet completely solved" said Cédric Blanpain, the senior and corresponding author of the Nature Cell Biology paper.

In conclusion, this new study, published in the online early edition of Nature Cell Biology, identifies a new multipotent stem cell population in the prostate tissue that ensure its postnatal development.

This work was supported by the FNRS, TELEVIE, the program d'excellence CIBLES of the Wallonia Region, a research grant from the Fondation Contre le Cancer, the ULB Fondation, the Fond Gaston Ithier. Cédric Blanpain is an investigator of Welbio and is supported by a starting grant of the European Research Council (ERC) and the EMBO Young Investigator Program


Story Source:

The above story is based on materials provided by Libre de Bruxelles, Université. Note: Materials may be edited for content and length.


Journal Reference:

  1. Marielle Ousset, Alexandra Van Keymeulen, Gaëlle Bouvencourt, Neha Sharma, Younes Achouri, Benjamin D. Simons, Cédric Blanpain. Multipotent and unipotent progenitors contribute to prostate postnatal development. Nature Cell Biology, 2012; DOI: 10.1038/ncb2600

Cite This Page:

Libre de Bruxelles, Université. "Identification of stem cells that contribute to prostate development." ScienceDaily. ScienceDaily, 15 October 2012. <www.sciencedaily.com/releases/2012/10/121015085026.htm>.
Libre de Bruxelles, Université. (2012, October 15). Identification of stem cells that contribute to prostate development. ScienceDaily. Retrieved July 29, 2014 from www.sciencedaily.com/releases/2012/10/121015085026.htm
Libre de Bruxelles, Université. "Identification of stem cells that contribute to prostate development." ScienceDaily. www.sciencedaily.com/releases/2012/10/121015085026.htm (accessed July 29, 2014).

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