Early but not late pregnancy induces lifelong reductions in the proportion of mammary progesterone sensing cells and epithelial Wnt signaling.

Abstract

Early pregnancy has a strong and lifelong protective effect against breast cancer in humans and rodents [1-3]. This breast cancer protective effect is diminished or even reversed after late pregnancy [4]. As a potential mechanism for the early parity-induced protective effect, we and others have demonstrated that early parity induces differentiation of mammary epithelial cells [5-7]. Furthermore, early parity downregulates the Wnt/Notch signaling ratio and the in vitro and in vivo proliferation potential of basal stem/progenitor cells in mice [6,7]. These early parity-induced changes of gene expression and dynamics of mammary stem/progenitor cells were caused primarily by a decrease in the proportion of hormone-sensitive and Wnt4-secreting luminal epithelial cells [6,7]. Although the reported findings provided a valid explanation for the breast cancer protective effect of an early pregnancy, two important questions remained unanswered. First, the early parity-induced cellular and molecular changes in mammary epithelium were investigated at a single time point (tissue/cell harvest at 40 days after weaning), leaving the question of their persistence unanswered. Second, mice were always mated at the young age of 6 weeks, and hence the effects of late pregnancy were not addressed. To directly answer these open questions, we performed additional experiments in old mice (22 months old) that had completed an early pregnancy at 6 weeks and in mice that had gone through late pregnancy (mating at 24 weeks). As markers for the parity-induced decrease in mammary gland hormone responsiveness and the reduction of basal epithelial Wnt signaling [6], immunohistochemistry in mammary gland sections was performed for progesterone receptor (PR)-positive cells and for Wnt target gene expression (versican and keratin 15 [8]) as well as for epithelial cells expressing nuclear beta-catenin. Furthermore, Wnt4 expression was compared between mammary gland tissues of parous and age-matched virgin control mice. The results demonstrate that early pregnancy-induced reductions in the proportion of PR-positive cells and expression of basal epithelial Wnt targets versican and keratin 15 persist into advanced age, and thus are of lifelong duration in mice (Figure 1A). Furthermore, pregnancy occurring at a very late age had only marginal or even no effects on PR-positive cells and expression of Wnt targets versican and keratin 15 (Figure 1B). We also noticed changes in the proportion of PR-positive cells upon aging in nulliparous mice. However, because the data in the studies on 22-month-old mice with early pregnancy and 8-month-old mice with late pregnancy were derived from two independent experiments, no direct conclusions can be drawn for the effect of age per se on the proportion of PR-positive cells in nulliparous control mice. Figure 1 Effects of early and late parity on hormone (progesterone) sensitive cells and Wnt target gene (versican and keratin 15) expression in mice. (A) Early parity-induced decrease in expression of progesterone receptor (PR) and Wnt target genes versican and ... To further substantiate a persistent decrease of epithelial Wnt signaling by early parity, we extended the analysis to beta-catenin, a marker for active Wnt signaling. We found a persistent decrease in the proportion of nuclear beta-catenin-positive mammary epithelial cells from 11.1 ± 1.5% in 22-month-old age-matched virgins to 6.7 ± 0.9% in 22-month-old mice that had gone through pregnancy at an early age. In contrast, nuclear beta-catenin in epithelial cells was not affected by late pregnancy (10.8 ± 1.3% in age-matched virgins versus 9.6 ± 1.9% in parous mice) (data represent the mean ± standard deviation of 3,000 counted cells from six mice per group). Furthermore, we had previously shown that decreases in PR-positive cells were associated with decreases in Wnt4 expression, which in turn was associated with decreased Wnt signaling in basal stem/progenitor cells [6]. Consistent with the data for PR, the basal epithelial Wnt targets versican and keratin 15; and for nuclear beta-catenin in epithelial cells, Wnt4 expression was also persistently reduced after early pregnancy but remained unchanged after late pregnancy (Figure 1C). Together with the previously reported study [6], the findings presented here represent the first direct comparison of the effects of early and late pregnancy on hormone sensing cells and on epithelial Wnt signaling in the mammary gland. The data conform with the presence of parity-induced changes in the dynamics of mammary cell functions upon early pregnancy [9] and suggest their absence upon late pregnancy in mice [10,11]. Overall these results are fully consistent with the lifelong breast cancer protective effect of early but not late pregnancy in humans [7]. They reinforce the validity of the adopted mouse model to study prevention strategies against human breast cancer and highlight the need for further investigations into the molecular changes following late versus early pregnancy.