Department of Pediatrics, Children's Nutrition Research Center, US Department of Agriculture/Agricultural Research Service, Baylor College of Medicine, Houston, TX 77030, USA.
Am J Physiol Endocrinol Metab. 2012 Aug 1;303(3):E365-76. doi: 10.1152/ajpendo.00175.2012. Epub 2012 May 29.
Lactose synthesis is believed to be rate limiting for milk production. However, understanding the molecular events controlling lactose synthesis in humans is still rudimentary. We have utilized our established model of the RNA isolated from breast milk fat globule from seven healthy, exclusively breastfeeding women from 6 h to 42 days following delivery to determine the temporal coordination of changes in gene expression in the carbohydrate metabolic processes emphasizing the lactose synthesis pathway in human mammary epithelial cell. We showed that milk lactose concentrations increased from 75 to 200 mM from 6 to 96 h. Milk progesterone concentrations fell by 65% at 24 h and were undetectable by day 3. Milk prolactin peaked at 36 h and then declined progressively afterward. In concordance with lactose synthesis, gene expression of galactose kinase 2, UDP-glucose pyrophosphorylase 2 (UGP2), and phosphoglucomutase 1 increased 18-, 10-, and threefold, respectively, between 6 and 72 h. Between 6 and 96 h, gene expression of UDP-galactose transporter 2 (SLC35A2) increased threefold, whereas glucose transporter 1 was unchanged. Gene expression of lactose synthase no. 3 increased 1.7-fold by 96 h, whereas α-lactalbumin did not change over the entire study duration. Gene expression of prolactin receptor (PRLR) and its downstream signal transducer and activator of transcription complex 5 (STAT5) were increased 10- and 2.5-fold, respectively, by 72 h. In summary, lactose synthesis paralleled the induction of gene expression of proteins involved in UDP-galactose synthesis and transport, suggesting that they are potentially rate limiting in lactose synthesis and thus milk production. Progesterone withdrawal may be the signal that triggers PRLR signaling via STAT5, which may in turn induce UGP2 and SLC35A2 expression.
乳糖合成本身被认为是乳汁生成的限速步骤。然而,对于控制人类乳糖合成的分子事件的理解仍然很初步。我们利用从 7 位健康、全母乳喂养的妇女分娩后 6 小时至 42 天的乳脂球中分离的 RNA 建立的模型,来确定碳水化合物代谢过程中基因表达的时空调控,重点是人类乳腺上皮细胞中的乳糖合成途径。我们发现,乳汁中的乳糖浓度从 6 小时至 96 小时从 75mM 增加到 200mM。乳汁中的孕酮浓度在 24 小时下降 65%,第 3 天检测不到。乳汁中的催乳素在 36 小时达到峰值,然后逐渐下降。与乳糖合成一致,半乳糖激酶 2、UDP-葡萄糖焦磷酸化酶 2 (UGP2) 和磷酸葡萄糖变位酶 1 的基因表达在 6 小时至 72 小时之间分别增加了 18 倍、10 倍和 3 倍。在 6 小时至 96 小时之间,UDP-半乳糖转运体 2 (SLC35A2) 的基因表达增加了 3 倍,而葡萄糖转运体 1 不变。乳糖合酶 3 的基因表达在 96 小时增加了 1.7 倍,而α-乳白蛋白在整个研究期间没有变化。催乳素受体 (PRLR) 和其下游信号转导和转录激活因子 5 (STAT5) 的基因表达在 72 小时分别增加了 10 倍和 2.5 倍。总之,乳糖合成与参与 UDP-半乳糖合成和转运的蛋白质的基因表达诱导平行,这表明它们可能是乳糖合成和乳汁生成的限速步骤。孕酮的撤退可能是通过 STAT5 触发 PRLR 信号的信号,这可能反过来诱导 UGP2 和 SLC35A2 的表达。