Kass Laura, Durando Milena, Ramos Jorge G, Varayoud Jorgelina, Powell Charles E, Luque Enrique H, Muñoz-de-Toro Mónica
Laboratorio de Endocrinología y Tumores Hormonodependientes, School of Biochemistry and Biological Sciences, Universidad Nacional del Litoral, C.C. 242, (3000) Santa Fe, Argentina.
J Steroid Biochem Mol Biol. 2004 Jun;91(1-2):29-39. doi: 10.1016/j.jsbmb.2004.02.001.
In this study, we investigated the cellular and molecular events involved in parity-related alterations in mammary gland (MG) proliferation and differentiation. Rat MGs were removed on day 9 of either first (nulliparous), second (primiparous) or third (multiparous) pregnancy. Expression of steroid hormone receptors along with cellular biomarkers of proliferation and differentiation were quantified in all MG tissue compartments by immunohistochemistry. Wnt-4 (a Wingless-like morphogenic gene involved in MG development), ERbeta and ERbeta2 mRNA were evaluated by RT-PCR analysis. Serum levels of mammotrophic hormones were measured. In comparison to nulliparous and primiparous rats, multiparous animals exhibited decreased luminal cell proliferation and PR levels, whereas alpha-lactalbumin, ERalpha, ERbeta and ERbeta2 expression were increased. In myoepithelial cells, while parity induced a decrease in proliferative activity, subsequent pregnancies and lactations lead to an increased state of differentiation. Our results showed that at least two periods of pregnancy and lactation were necessary to modify the studied parameters. The lower proliferative activity and higher differentiation state of the multiparous MG are associated with both a decreased PR expression and increased ERalpha and ERbeta expression. Since ERbeta and/or ERbeta2 isoform expression was related to parity history, results suggest that the decreased proliferative activity and PR expression observed in the MG of multiparous animals may be associated with overexpression of ERbeta and/or the ERbeta2 isoform, thereby antagonizing the proliferative effects associated with ERalpha.
在本研究中,我们调查了乳腺(MG)增殖和分化过程中与生育相关变化所涉及的细胞和分子事件。在首次(未生育)、第二次(初产)或第三次(经产)妊娠的第9天切除大鼠乳腺。通过免疫组织化学对所有乳腺组织区室中类固醇激素受体的表达以及增殖和分化的细胞生物标志物进行定量。通过逆转录-聚合酶链反应(RT-PCR)分析评估Wnt-4(一种参与乳腺发育的无翅型形态发生基因)、雌激素受体β(ERβ)和雌激素受体β2(ERβ2)的mRNA。测量促乳腺激素的血清水平。与未生育和初产大鼠相比,经产动物的管腔细胞增殖和孕激素受体(PR)水平降低,而α-乳白蛋白、雌激素受体α(ERα)、ERβ和ERβ2的表达增加。在肌上皮细胞中,虽然生育会导致增殖活性降低,但随后的妊娠和哺乳会导致分化状态增加。我们的结果表明,至少需要两个妊娠和哺乳周期才能改变所研究的参数。经产乳腺较低的增殖活性和较高的分化状态与PR表达降低以及ERα和ERβ表达增加有关。由于ERβ和/或ERβ2亚型的表达与生育史相关,结果表明,在经产动物乳腺中观察到的增殖活性和PR表达降低可能与ERβ和/或ERβ2亚型的过表达有关,从而拮抗与ERα相关的增殖作用。