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Biology of Reproduction 66, 1471-1476 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Concurrent Pregnancy Retards Mammary Involution: Effects on Apoptosis and Proliferation of the Mammary Epithelium after Forced Weaning of Mice1

Anthony V. Capucoa, Minglin Lib, Ezhou Longd, Shuxun Renb, Kathleen S. Hruskab, Kristel Schorrb, and Priscilla A. Furthb,c

a Gene Evaluation and Mapping Laboratory, U.S. Department of Agriculture, Agricultural Research Service, Beltsville, Maryland 20705 b Departments of Medicine c Physiology, Institute of Human Virology, University of Maryland Medical School, Baltimore, Maryland 21201 d Department of Animal Science, McGill University, Montreal, Quebec, Canada H9X 3V9

The effect of pregnancy on postweaning mammary gland involution was investigated in mice. On the third day after forced weaning at Lactation Day 10, the apoptotic index was 56% lower in mammary tissue of mice that were pregnant at the time of weaning than in nonpregnant mice. Conversely, the bromodeoxyuridine-labeling index was increased sevenfold in pregnant mice compared to nonpregnant controls (3.5% vs. 0.5%, respectively). Structure of mammary alveoli was largely maintained in postweaning pregnant mice. The effect of pregnancy on three specific mammary epithelial cell survival pathways was also examined. First, pregnancy blocked the loss of Stat5a phosphorylation during involution. Significantly, loss of Stat5a phosphorylation during involution was not correlated with loss of Stat5a nuclear localization. Second, pregnancy maintained nuclear-localized progesterone receptor during lactation. Third, pregnancy was associated with increased expression of bfl-1 during involution but had little effect on the expression of other bcl-2 family members. The data indicate that pregnancy inhibits mammary cell apoptosis after weaning while permitting proliferation of the mammary epithelium, and they support the hypothesis that Stat5a and progesterone-signaling pathways act in concert to mediate this effect.

First decision: 26 November 2001.

1 Supported by the Department of Defense Breast Cancer Research Program BC000716 (P.A.F.), National Institutes of Health CA68033 (P.A.F.), and U.S. Department of Agriculture-Agricultural Research Service CRIS 1265-31000-0047 (A.V.C.).

2 Correspondence: Anthony V. Capuco, Gene Evaluation and Mapping Lab, Bldg. 200, BARC-East, Beltsville, MD 20705. FAX: 301 504 8414; acapuco{at}anri.barc.usda.gov




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