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Sexual Dimorphism of Pancreatic β-Cell Degeneration in Transgenic Mice Expressing an Insulin-ras Hybrid Gene^*

Department of Molecular Pharmacology, Albert Einstein College of Medicine Bronx, New York 10461

Address requests for reprints to: Dr. Shimon Efrat, Department of Molecular Pharmacology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York 10461.

Abstract

The human H-ras oncogene induces cell degeneration and diabetes when expressed in pancreatic β-cells in transgenic mice. The disease develops predominantly in male mice between 5–8 months of age. Most transgenic female mice do not manifest this phenotype, even at much greater ages. However, ovariectomy induces female β-cell degeneration similar to that in the males. In contrast, castration or the presence of the testicular feminization mutation do not alter the course of the disease in males. Treatment of males and ovariectomized females with estrogen prevents the development of diabetes. These results suggest that testicular androgens and a functional testosterone receptor are not required for the increased susceptibility of male β-cells to the effects of the Ras oncoprotein, and that the relative resistance of female β-cells is mediated by estrogen. In addition, a genetic component of female β-cell resistance to Ras is revealed by crossing the transgenic mice with C3HeB/FeJ mice, which results in a pronounced increase in the incidence of female diabetes. (Endocrinology 128: 897– 901, 1991)

Footnotes

^* This work was supported by the Juvenile Diabetes Foundation and core grants from the Diabetes and Cancer Centers of Albert Einstein College of Medicine.

Received August 28, 1990.

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