Piantoni Paola, Wang Ping, Drackley James K, Hurley Walter L, Loor Juan J
Mammalian NutriPhysioGenomics.
Bioinform Biol Insights. 2010 Sep 20;4:85-97. doi: 10.4137/bbi.s5850.
Histological and functional changes associated with involution in the mammary gland are partly regulated by changes in gene expression. At 42 d postpartum, Holstein cows underwent a period of 5 d during which they were milked 1X daily until complete cessation of milking. Percutaneous mammary biopsies (n = 5/time point) were obtained on d 1, 5, 14, and 21 relative to the start of 1X milking for transcript profiling via qPCR of 57 genes associated with metabolism, apoptosis/proliferation, immune response/inflammation, oxidative stress, and tissue remodeling. Not surprisingly, there was clear downregulation of genes associated with milk fat synthesis (FASN, ACACA, CD36, FABP3, SCD) and lipid-related transcription regulation (SREBF1, SREBF2). Similar to milk fat synthesis-related genes, those encoding proteins required for glucose uptake (SLC2A1), casein synthesis (CSN2, CSN3), and lactose synthesis (LALBA) decreased during involution. Unlike metabolic genes, those associated with immune response and inflammation (C3, LTF, SAA3), oxidative stress (GPX1, SOD2), and pro-inflammatory cytokine signaling (SPP1, TNF) increased to peak levels by d 14 from the start of 1X milking. These adaptations appeared to be related with tissue remodeling as indicated by upregulation of proteins encoding matrix proteinases (MMP2), IGFBP3, and transcriptional regulation of apoptosis/cell proliferation (MYC). In contrast, the concerted upregulation of STAT3, TGFB1, and TGFB1R during the first 14 d was suggestive of an activation of these signaling pathways probably as an acute response to regulate differentiation and/or mammary cell survival upon the onset of a marked pro-inflammatory and oxidative stress response induced by the gradual reduction in milk removal. Results suggest a central role of STAT3, MYC, PPARG, SREBF1, and SREBF2 in regulating concerted alterations in metabolic and cell survival mechanisms, which were induced partly via oxidative stressed-triggered inflammation and the decline in metabolic activity.
乳腺退化相关的组织学和功能变化部分受基因表达变化的调控。产后42天,荷斯坦奶牛经历了为期5天的阶段,在此期间,它们每天挤奶1次,直至完全停止挤奶。在相对于每天挤奶1次开始后的第1、5、14和21天,进行经皮乳腺活检(每个时间点n = 5),通过qPCR对57个与代谢、凋亡/增殖、免疫反应/炎症、氧化应激和组织重塑相关的基因进行转录谱分析。不出所料,与乳脂肪合成相关的基因(FASN、ACACA、CD36、FABP3、SCD)和脂质相关转录调控基因(SREBF1、SREBF2)明显下调。与乳脂肪合成相关基因类似,那些编码葡萄糖摄取所需蛋白质(SLC2A1)、酪蛋白合成(CSN2、CSN3)和乳糖合成(LALBA)的基因在退化过程中也减少。与代谢基因不同,那些与免疫反应和炎症相关的基因(C3、LTF、SAA3)、氧化应激相关基因(GPX1、SOD2)以及促炎细胞因子信号相关基因(SPP1、TNF)从每天挤奶1次开始到第14天增加到峰值水平。这些适应性变化似乎与组织重塑有关,这表现为编码基质蛋白酶(MMP2)、IGFBP3的蛋白质上调以及凋亡/细胞增殖的转录调控(MYC)。相反,在最初的14天内STAT3、TGFB1和TGFB1R的协同上调表明这些信号通路被激活,这可能是对乳汁排出逐渐减少所诱导的明显促炎和氧化应激反应的急性反应,以调节分化和/或乳腺细胞存活。结果表明,STAT3、MYC、PPARG、SREBF1和SREBF2在调节代谢和细胞存活机制的协同改变中起核心作用,这些改变部分是由氧化应激引发的炎症和代谢活性下降所诱导的。