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This version published online on May 26, 2005
Endocrinology, doi:10.1210/en.2005-0340
A more recent version of this article appeared on September 1, 2005
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Submitted on March 21, 2005
Accepted on May 17, 2005

Perinatal exposure to Bisphenol A alters peripubertal mammary gland development in mice

Monica Munoz-de-Toro, Caroline Markey, Perinaaz R. Wadia, Enrique H. Luque, Beverly S. Rubin, Carlos Sonnenschein, and Ana M. Soto*

Department of Anatomy and Cellular Biology, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111; Laboratorio de Endocrinologia y Tumores Hormonodependientes, Faculty of Biochemistry and Biological Sciences, Universidad Nacional del Litoral, 3000 Santa Fe, Argentina

* To whom correspondence should be addressed. E-mail: ana.soto{at}tufts.edu.

Developmental exposure to estrogenic chemicals induces morphological, functional and behavioral anomalies associated with reproduction. Humans are exposed to bisphenol-A (BPA), an estrogenic compound that leaches from dental materials and plastic food and beverage containers. The aim of the present study was to determine the effects of perinatal exposure to low, environmentally relevant doses of BPA (25 and 250 ng BPA/kg body weight (bw)/day) on the peripubertal development of the mammary gland. BPA exposure enhanced the mammary glands' sensitivity to estradiol in ovariectomized CD-1 mice. In their intact 30-day-old littermates, the area and numbers of terminal end buds relative to the gland ductal area increased while their apoptotic activity decreased. There was a positive correlation between ductal length and the age at first proestrus; that was reduced as the BPA dose increased, suggesting that BPA exposure slows down ductal invasion of the stroma. There was also a significant increase of progesterone receptor-positive ductal epithelial cells that were localized in clusters, suggesting future branching points. Indeed, lateral branching was significantly enhanced at 4 months of age in mice exposed to 25 ng BPA /kg bw/day. In conclusion, perinatal exposure to environmentally relevant BPA doses results in persistent alterations in mammary gland morphogenesis. Of special concern is the increased terminal end bud density at puberty as well as the increased number of terminal ends reported previously in adult animals, since these two structures are the sites where cancer arises in humans and rodents.


Key words: endocrine disruptors • bisphenol-A • xenoestrogens • mammary gland development • puberty • terminal end buds • ductal growth




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