胰岛素样生长因子结合蛋白7的缺失导致泌乳期小鼠乳腺过早退化。
Loss of Igfbp7 causes precocious involution in lactating mouse mammary gland.
作者信息
Chatterjee Sumanta, Bacopulos Stephanie, Yang Wenyi, Amemiya Yutaka, Spyropoulos Demetri, Raouf Afshin, Seth Arun
机构信息
Department of Immunology, University of Manitoba, Winnipeg, Canada ; Manitoba Institute of Cell Biology, Winnipeg, Manitoba, Canada.
Biological Sciences Platform, Sunnybrook Research Institute and Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
出版信息
PLoS One. 2014 Feb 4;9(2):e87858. doi: 10.1371/journal.pone.0087858. eCollection 2014.
BACKGROUND
Insulin like growth factors (IGFs) and their binding proteins (IGFBPs) are secreted peptides that play major roles in regulating the normal development and maturation of mammary gland. While Igfbp7 has been shown to decrease breast tumor growth, its role in regulating the normal mammary gland development has not been studied. To this end, we generated Igfbp7-null mice and examined the development and maturation of mammary glands in the virgin, pregnant and lactating animals.
RESULTS
We report here that loss of Igfbp7 significantly retards mammary gland development in the virgin animals. More significantly, the pregnant Igfpb7-null glands contained fewer alveolar structures and that during lactation these glands exhibit the morphological changes that are associated with involution. The transcriptome profile of the Igfbp7-null glands on the lactation day 3 revealed a distinct involution-related gene signature compared to the lactating WT glands. Interestingly, we found that the lactating Igfbp7-null glands exhibit increased expression of Stat3 and enhanced activation of (phosphorylated) Stat3, combined with decreased expression of Stat5 suggesting that the absence of Igfbp7 accelerates the onset of involution. We also found that in absence of Igfpb7, the lactating glands contain increased Igfbp5 protein along with decreased expression of IGF-1 Receptor and Akt activation. Finally, we show that during the normal course of involution, Igfbp7 expression is significantly decreased in the mammary gland.
CONCLUSION
Our data suggest that loss of Igfbp7 induces precocious involution possibly through diminished cell survival signals. Our findings identify Igfbp7 as major regulator of involution in the mammary gland.
背景
胰岛素样生长因子(IGFs)及其结合蛋白(IGFBPs)是分泌性肽,在调节乳腺的正常发育和成熟过程中发挥着重要作用。虽然已有研究表明Igfbp7可抑制乳腺肿瘤生长,但其在调节正常乳腺发育中的作用尚未见报道。为此,我们构建了Igfbp7基因敲除小鼠,并检测了未孕、妊娠和哺乳期动物乳腺的发育和成熟情况。
结果
我们在此报告,Igfbp7缺失显著延缓了未孕动物的乳腺发育。更显著的是,妊娠的Igfpb7基因敲除小鼠的乳腺中腺泡结构较少,并且在哺乳期这些乳腺呈现出与退化相关的形态学变化。与哺乳期野生型小鼠的乳腺相比,在哺乳期第3天Igfbp7基因敲除小鼠的乳腺转录组图谱显示出明显的与退化相关的基因特征。有趣的是,我们发现哺乳期Igfbp7基因敲除小鼠的乳腺中Stat3表达增加且(磷酸化的)Stat3激活增强,同时Stat5表达降低,这表明Igfbp7的缺失加速了退化的开始。我们还发现,在没有Igfpb7的情况下,哺乳期乳腺中Igfbp5蛋白增加,同时IGF-1受体表达降低且Akt激活减少。最后,我们表明在正常的退化过程中,乳腺中Igfbp7的表达显著降低。
结论
我们的数据表明,Igfbp7的缺失可能通过减少细胞存活信号诱导早熟退化。我们的研究结果确定Igfbp7是乳腺退化的主要调节因子。