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白血病抑制因子诱导乳腺上皮细胞凋亡并参与小鼠乳腺退化。

Leukemia inhibitory factor induces apoptosis of the mammary epithelial cells and participates in mouse mammary gland involution.

作者信息

Schere-Levy Carolina, Buggiano Valeria, Quaglino Ana, Gattelli Albana, Cirio Maria Cecilia, Piazzon Isabel, Vanzulli Silvia, Kordon Edith C

机构信息

ILEX-CONICET División de Medicina Experimental, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina, Buenos Aires, Argentina.

出版信息

Exp Cell Res. 2003 Jan 1;282(1):35-47. doi: 10.1006/excr.2002.5666.

Abstract

Leukemia inhibitory factor (LIF) is a multifunctional glycoprotein that displays multiple biological activities in different cell types, but to date there has been no report on its expression in the normal mammary gland. In this study we found that LIF is expressed at low but detectable levels in postpubertal, adult virgin, and pregnant mouse mammary glands. However, LIF expression drops after parturition to become almost undetectable in lactating glands. Interestingly, LIF expression shows a steep increase shortly after weaning that is maintained for the following 3 days. During this period, known as the first stage of mammary gland involution, the lack of suckling induces local factors that cause extensive epithelial cell death. It has been shown that Stat3 is the main factor in signaling the initiation of apoptosis, but the mechanism of its activation remains unclear. Herein, we show that LIF expression in the gland is induced by milk stasis and not by the decrease of circulating lactogenic hormones after weaning. Implantation of LIF containing pellets in lactating glands results in a significant increase in epithelium apoptosis. In addition, this treatment also induces Stat3 phosphorylation. We conclude that LIF regulated expression in the mouse mammary gland may play a relevant role during the first stage of mammary gland involution. Our results also show that LIF-induced mammary epithelium apoptosis could be mediated, at least partially, by Stat3 activation.

摘要

白血病抑制因子(LIF)是一种多功能糖蛋白,在不同细胞类型中表现出多种生物学活性,但迄今为止,尚无关于其在正常乳腺中表达的报道。在本研究中,我们发现LIF在青春期后、成年未孕及怀孕小鼠的乳腺中以低水平但可检测到的方式表达。然而,分娩后LIF表达下降,在泌乳期乳腺中几乎检测不到。有趣的是,断奶后不久LIF表达急剧增加,并在接下来的3天内维持这种状态。在此期间,即乳腺退化的第一阶段,缺乏哺乳会诱导局部因子导致广泛的上皮细胞死亡。已经表明Stat3是启动细胞凋亡信号的主要因子,但其激活机制仍不清楚。在此,我们表明乳腺中LIF的表达是由乳汁淤积诱导的,而不是断奶后循环泌乳激素的减少所诱导。在泌乳期乳腺中植入含LIF的微丸会导致上皮细胞凋亡显著增加。此外,这种处理还会诱导Stat3磷酸化。我们得出结论,LIF在小鼠乳腺中的调节表达可能在乳腺退化的第一阶段发挥相关作用。我们的结果还表明,LIF诱导的乳腺上皮细胞凋亡可能至少部分由Stat3激活介导。

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