Species-Specific Detection of Growth Factor Gene Expression in Developing Murine Prostatic Tissue
The aim of the present study was to develop a method by which the expression of paracrine signaling molecules could be localized to either epithelial or stromal cells of developing prostatic tissue. Heterospecific tissue recombinants composed of mouse urogenital epithelium (mouse UGE) plus rat uroge...
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Published in: | Biology of reproduction Vol. 59; no. 1; pp. 93 - 99 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Madison, WI
Society for the Study of Reproduction
01-07-1998
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Subjects: | |
Online Access: | Get full text |
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Summary: | The aim of the present study was to develop a method by which the expression of paracrine signaling molecules could be localized
to either epithelial or stromal cells of developing prostatic tissue. Heterospecific tissue recombinants composed of mouse
urogenital epithelium (mouse UGE) plus rat urogenital mesenchyme (rat UGM) and the reciprocal tissue recombinants, rat urogenital
epithelium (rat UGE) plus mouse urogenital mesenchyme (mouse UGM), were grafted under the renal capsule in intact, athymic
male mouse and rat hosts. After 2 wk of growth, RNA from the grafts was analyzed by species-specific reverse transcription-polymerase
chain reaction for the expression of the mRNA for the following molecules: transforming growth factors β1, β3, and α; epidermal
growth factor; epidermal growth factor receptor; and keratinocyte growth factor. The species of expression of these growth
factor and receptor gene products within the heterospecific tissue recombinants was identified, allowing determination of
the cell layer in which the genes were expressed. Identification of the tissue-specific expression of the growth factor and
growth factor receptor profiles of the epithelium and mesenchyme of this in vivo model provides a basis for understanding
the autocrine and paracrine mediators of cell-cell interactions in prostatic development. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod59.1.93 |