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Official websites use. Share sensitive information only on official, secure websites. Correspondence to: Roland P. Bourette, roland. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Isolation of prostate stem cells PSCs is crucial for understanding their biology during normal development and tumorigenesis.
In this aim, we used a transgenic mouse model expressing GFP from the stem cell-specific s-SHIP promoter to mark putative stem cells during postnatal prostate development.
Here we show that cells identified by GFP expression are present transiently during early prostate development and localize to the basal cell layer of the epithelium.
Altogether, these results demonstrate that s-SHIP promoter expression is a new marker for neonatal basal prostate cells exhibiting stem cell properties that enables PSCs in situ identification and isolation via a single consistent parameter. It also identified stem cell regulators with potential applications for further analyses of normal and cancer stem cells. Most tissues contain a small dedicated stem cell population, which is essential for maintaining tissue homeostasis and for tissue repair after injury [ 1 , 2 ].
Adult tissue stem cells also may contribute to cancer development as being the cells of origin in cancer or tumor-initiating cells [ 3 ]. Therefore, these adult stem cells provide an enormous advantage to survival of the adult organism through tissue maintenance, regeneration and repair; but at the same time, they may represent a risk to the tissue or organism due to potential cancer development [ 4 ].