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Cell-specific expression of kidney androgen-regulated protein messenger RNA is under multihormonal control
1Population Council, New York, New York 10021.
Abstract:
Kidney androgen-regulated protein (KAP) gene expression is under androgenic control in the epithelial cells of the proximal convoluted tubule in the mouse kidney. In Tfm/Y androgen receptor-deficient mice, KAP mRNA was detected by in situ hybridization in a subpopulation of these cells only in the S3 segment of the proximal tubules in the outer medulla. Treatment of Tfm/Y animals with testosterone caused a partial induction of KAP mRNA levels, while dihydrotestosterone had no effect. These data suggested that the androgen receptor-independent induction of KAP gene expression in these animals was mediated by an estrogenic metabolite of testosterone, since dihydrotestosterone cannot be aromatized to an estrogenic form. Estrogen treatment of Tfm/Y mice caused an increase in KAP gene expression similar to that observed with testosterone. However, ovariectomy of normal female mice did not eliminate KAP gene expression in the S3 cells and, in fact, resulted in a slight increase. Adrenalectomy in combination with castration had no effect on KAP mRNA levels in S3 cells. However, hypophysectomy alone completely eliminated this cell-specific component of KAP gene expression. These results indicate that KAP gene expression is subject to cell-specific regulation in different segments of the proximal tubule and that this regulation is mediated by hormones of both gonadal and pituitary origin.
Insights
Kidney androgen-regulated protein (KAP) gene expression in mice is regulated by pituitary hormones and gonadal steroids. This regulation occurs independently of the androgen receptor in specific kidney tubule cells.
Area of Science:
- Endocrinology
- Molecular Biology
- Nephrology
Background:
- Kidney androgen-regulated protein (KAP) gene expression is typically controlled by androgens in mouse kidney proximal convoluted tubule epithelial cells.
- Androgen receptor-deficient (Tfm/Y) mice exhibit KAP mRNA in a specific subpopulation of S3 segment cells.
Purpose of the Study:
- To investigate the hormonal regulation of KAP gene expression in mouse kidney.
- To elucidate the role of androgen receptor-independent pathways and other hormones in KAP regulation.
Main Methods:
- In situ hybridization to detect KAP mRNA.
- Hormone treatments (testosterone, dihydrotestosterone, estrogen) in Tfm/Y mice.
- Surgical interventions (ovariectomy, adrenalectomy, castration, hypophysectomy) in mice.
Main Results:
- Testosterone partially induced KAP mRNA in Tfm/Y mice, suggesting an androgen receptor-independent mechanism.
- Estrogen mimicked testosterone's effect, indicating potential mediation by an estrogenic metabolite.
- KAP expression persisted after ovariectomy and was slightly increased, while hypophysectomy completely abolished S3 cell KAP expression.
Conclusions:
- KAP gene expression is cell-specifically regulated in different proximal tubule segments.
- Hormonal regulation involves both gonadal steroids (potentially via metabolites) and pituitary hormones.
- Pituitary factors play a crucial role in maintaining KAP expression in S3 segment cells.