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适度高温条件通过控制STAT3和STAT5信号传导诱导乳腺上皮细胞的泌乳能力。

Moderate High Temperature Condition Induces the Lactation Capacity of Mammary Epithelial Cells Through Control of STAT3 and STAT5 Signaling.

作者信息

Kobayashi Ken, Tsugami Yusaku, Matsunaga Kota, Suzuki Takahiro, Nishimura Takahiro

机构信息

Laboratory of Cell and Tissue Biology, Research Faculty of Agriculture, Hokkaido University, North 9, West 9, Sapporo, 060-8589, Japan.

出版信息

J Mammary Gland Biol Neoplasia. 2018 Jun;23(1-2):75-88. doi: 10.1007/s10911-018-9393-3. Epub 2018 Apr 9.

Abstract

In lactating mammary glands, alveolar mammary epithelial cells (MECs) synthesize and secrete milk components. MECs also form less permeable tight junctions (TJs) to prevent the leakage of milk components. During lactation, MECs are exposed to temperature changes by metabolic heat production and air ambient temperature. In this study, we investigated whether temperature changes influence milk production ability and TJ barriers in MECs by using two lactating culture models. The results showed that 39 °C treatment activated milk production and enhanced the formation of less-permeable TJs. In contrast, 41 °C treatment caused adverse effects on the TJ barrier and cell viability, although the milk production ability of MECs was temporarily up-regulated. MECs cultured at 37 °C showed relatively low milk production ability and high proliferation activity. Furthermore, we investigated three kinds of transcription factors relating to lactogenesis, signal transducer and activator of transcription 5 (STAT5), STAT3 and glucocorticoid receptor (GR). STAT5 signaling was activated at 39 and 41 °C by an increase in total STAT5. However, long-term treatment led to a decrease in total STAT5. STAT3 signaling was inactivated by high temperature treatment through a decrease in total STAT3 and inhibited phosphorylation of STAT3. GR signaling was continuously activated regardless of temperature. These results indicate that a moderate high temperature condition at 39 °C induces a high lactation capacity of MECs through control of STAT5 and STAT3 signaling. In contrast, long-term exposure at 41 °C leads to a decline in milk production capacity by inactivation of STAT5 and a decrease in the total number of MECs.

摘要

在泌乳乳腺中,腺泡乳腺上皮细胞(MECs)合成并分泌乳汁成分。MECs还形成通透性较低的紧密连接(TJs),以防止乳汁成分泄漏。在泌乳期间,MECs会因代谢产热和环境气温变化而暴露于温度变化之中。在本研究中,我们通过使用两种泌乳培养模型,研究了温度变化是否会影响MECs的产奶能力和TJ屏障。结果表明,39°C处理激活了产奶能力,并增强了通透性较低的TJs的形成。相比之下,41°C处理对TJ屏障和细胞活力产生了不利影响,尽管MECs的产奶能力暂时上调。在37°C培养的MECs显示出相对较低的产奶能力和较高的增殖活性。此外,我们研究了与泌乳相关的三种转录因子,即信号转导和转录激活因子5(STAT5)、STAT3和糖皮质激素受体(GR)。STAT5信号在39°C和41°C时因总STAT5增加而被激活。然而,长期处理导致总STAT5减少。高温处理通过总STAT3减少和STAT3磷酸化受抑制使STAT3信号失活。GR信号无论温度如何都持续被激活。这些结果表明,39°C的适度高温条件通过控制STAT5和STAT3信号诱导MECs产生高泌乳能力。相比之下,长期暴露于41°C会导致STAT5失活和MECs总数减少,从而使产奶能力下降。

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