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Departments of Urology (W.Y.C., L.B., G.S.P.) and Physiology and Biophysics (G.S.P.), University of Illinois College of Medicine, Chicago, Illinois 60612; and VA Medical Center and Departments of Laboratory Medicine, Pathology and Surgical Oncology (M.J.W.), University of Minnesota, Minneapolis, Minnesota 55417
Address all correspondence and requests for reprints to: Gail S. Prins, Ph.D., Department of Urology, M/C 955, 820 South Wood Street, Chicago, Illinois 60612. E-mail: gprins{at}uic.edu
The purpose of this study was to examine whether changes in
extracellular matrix (ECM) molecules are associated with the growth
inhibition and differentiation defects of the prostate gland following
neonatal exposure to estradiol. Using immunocytochemistry (ICC),
laminin and collagen IV were localized to the basement membrane (BM) as
well to the basal lamina of the periductal smooth muscle of the control
developing prostates. In contrast, fibronectin and collagen III were
localized throughout the stromal ECM. Exposure to neonatal estrogen
altered the staining profile for specific ECM molecules. In the
estrogenized rats, a thick layer of cells negative for laminin and
collagen IV was observed adjacent to the BM. Electron microscopy and
ICC for
-actin, fibronectin, and vimentin identified this
multicellular layer of periductal cells as differentiated fibroblasts.
Peripheral to these fibroblasts, actin-positive smooth muscle formed a
second layer of periductal stromal cells. PCNA labeling showed that
estrogen exposure increased the fibroblast proliferation. Because many
periductal fibroblasts were positive for estrogen receptor
(ER
)
in estrogenized rats, a direct effect of estradiol on their
proliferation is suggested. Gelatinolytic gels revealed that estrogen
exposure did not alter the activity of matrix metalloproteinases
associated with tissue remodeling during prostate morphogenesis.
However, the periductal fibroblast layer in estrogenized prostates was
devoid of urokinase- and tissue-plasminogen activator, which may
potentially alter the localized proteolysis involved in matrix
remodeling. It is proposed that proliferation of a multicellular layer
of periductal fibroblasts in estrogenized prostates results in a
physical barrier that constrains branching morphogenesis and blocks
paracrine communications between smooth muscle and epithelial cells
which normally regulate differentiation.
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J. J. Bianco, S. J. McPherson, H. Wang, G. S. Prins, and G. P. Risbridger Transient Neonatal Estrogen Exposure to Estrogen-Deficient Mice (Aromatase Knockout) Reduces Prostate Weight and Induces Inflammation in Late Life Am. J. Pathol., June 1, 2006; 168(6): 1869 - 1878. [Abstract] [Full Text] [PDF] |
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L. Huang, Y. Pu, S. Alam, L. Birch, and G. S. Prins Estrogenic Regulation of Signaling Pathways and Homeobox Genes During Rat Prostate Development J Androl, May 1, 2004; 25(3): 330 - 337. [Full Text] [PDF] |
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J. G. Ramos, J. Varayoud, L. Kass, H. Rodriguez, L. Costabel, M. Munoz-de-Toro, and E. H. Luque Bisphenol A Induces Both Transient and Permanent Histofunctional Alterations of the Hypothalamic-Pituitary-Gonadal Axis in Prenatally Exposed Male Rats Endocrinology, July 1, 2003; 144(7): 3206 - 3215. [Abstract] [Full Text] [PDF] |
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J. J. Bianco, D. J. Handelsman, J. S. Pedersen, and G. P. Risbridger Direct Response of the Murine Prostate Gland and Seminal Vesicles to Estradiol Endocrinology, December 1, 2002; 143(12): 4922 - 4933. [Abstract] [Full Text] [PDF] |
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G. S. Prins, W. Y. Chang, Y. Wang, and R. B. van Breemen Retinoic Acid Receptors and Retinoids Are Up-Regulated in the Developing and Adult Rat Prostate by Neonatal Estrogen Exposure Endocrinology, September 1, 2002; 143(9): 3628 - 3640. [Abstract] [Full Text] [PDF] |
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S. Nilsson, S. Makela, E. Treuter, M. Tujague, J. Thomsen, G. Andersson, E. Enmark, K. Pettersson, M. Warner, and J.-A. Gustafsson Mechanisms of Estrogen Action Physiol Rev, October 1, 2001; 81(4): 1535 - 1565. [Abstract] [Full Text] [PDF] |
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J. G. Ramos, J. Varayoud, C. Sonnenschein, A. M. Soto, M. Munoz de Toro, and E. H. Luque Prenatal Exposure to Low Doses of Bisphenol A Alters the Periductal Stroma and Glandular Cell Function in the Rat Ventral Prostate Biol Reprod, October 1, 2001; 65(4): 1271 - 1277. [Abstract] [Full Text] [PDF] |
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G. S. Prins, L. Birch, J. F. Couse, I. Choi, B. Katzenellenbogen, and K. S. Korach Estrogen Imprinting of the Developing Prostate Gland Is Mediated through Stromal Estrogen Receptor {alpha}: Studies with {alpha}ERKO and {beta}ERKO Mice Cancer Res., August 1, 2001; 61(16): 6089 - 6097. [Abstract] [Full Text] [PDF] |
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N. Atanassova, C. McKinnell, K. Williams, K. J. Turner, J. S. Fisher, P. T. K. Saunders, M. R. Millar, and R. M. Sharpe Age-, Cell- and Region-Specific Immunoexpression of Estrogen Receptor {{alpha}} (But Not Estrogen Receptor {beta}) during Postnatal Development of the Epididymis and Vas Deferens of the Rat and Disruption of This Pattern by Neonatal Treatment with Diethylstilbestrol Endocrinology, February 1, 2001; 142(2): 874 - 886. [Abstract] [Full Text] [PDF] |
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H. Habermann, W. Y. Chang, L. Birch, P. Mehta, and G. S. Prins Developmental Exposure to Estrogens Alters Epithelial Cell Adhesion and Gap Junction Proteins in the Adult Rat Prostate Endocrinology, January 1, 2001; 142(1): 359 - 369. [Abstract] [Full Text] [PDF] |
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R. A. Jarred, B. Cancilla, G. S. Prins, K. A. Thayer, G. R. Cunha, and G. P. Risbridger Evidence That Estrogens Directly Alter Androgen-Regulated Prostate Development Endocrinology, September 1, 2000; 141(9): 3471 - 3477. [Abstract] [Full Text] [PDF] |
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J. T. Hamm, B. R. Sparrow, D. Wolf, and L. S. Birnbaum In Utero and Lactational Exposure to 2,3,7,8-Tetrachlorodibenzo-p-dioxin Alters Postnatal Development of Seminal Vesicle Epithelium Toxicol. Sci., April 1, 2000; 54(2): 424 - 430. [Abstract] [Full Text] [PDF] |
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W. Y. Chang, L. Birch, C. Woodham, L. I. Gold, and G. S. Prins Neonatal Estrogen Exposure Alters the Transforming Growth Factor-{beta} Signaling System in the Developing Rat Prostate and Blocks the Transient p21cip1/waf1 Expression Associated with Epithelial Differentiation Endocrinology, June 1, 1999; 140(6): 2801 - 2813. [Abstract] [Full Text] |
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