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Prostatic ductal system in rats: tissue-specific expression and regional variation in stromal distribution of transforming growth factor-beta 1.

Authors :
Nemeth JA
Sensibar JA
White RR
Zelner DJ
Kim IY
Lee C
Source :
The Prostate [Prostate] 1997 Sep 15; Vol. 33 (1), pp. 64-71.
Publication Year :
1997

Abstract

Background: Regional variations in stromal-epithelial interactions, mediated through soluble growth factors, may be responsible for differences in epithelial growth and death observed between regions of the rat prostatic ductal system. Since transforming growth factor-beta 1 (TGF-beta 1) can induce prostatic epithelial cell death in vitro and in vivo, we examined the localization and production of TGF-beta 1 with respect to the functional regions of the rat prostatic ductal system.<br />Methods: The distribution of TGF-beta 1 in the rat ventral prostate was examined by immunohistochemistry. Cell type-specific expression of TGF-beta 1 was determined using RT-PCR analysis of prostate epithelial and stromal cell fractions separated by Percoll gradient centrifugation.<br />Results: Immunohistochemical staining of normal prostate revealed regional variations in stromal TGF-beta 1 protein, which was most abundant in the stroma surrounding the degenerative proximal ducts. TGF-beta 1 staining was also tightly associated with the prostatic smooth muscle. Results of RT-PCR experiments confirmed the major source of TGF-beta 1 mRNA in normal rat prostate to be the stroma, with lesser expression by the epithelium.<br />Conclusions: Stromal TGF-beta 1 was associated with cell death in the adjacent epithelial cell compartment in the prostatic ductal system, and alpha-smooth muscle actin-positive stromal cells may play a negative growth-regulatory role in the rat ventral prostate through production of TGF-beta 1.

Details

Language :
English
ISSN :
0270-4137
Volume :
33
Issue :
1
Database :
MEDLINE
Journal :
The Prostate
Publication Type :
Academic Journal
Accession number :
9294629
Full Text :
https://doi.org/10.1002/(sici)1097-0045(19970915)33:1<64::aid-pros11>3.0.co;2-j