Zhou Miaomiao, Huang Fei, Qi Yehui
College of Agricultural Science and Engineering Liaocheng University Liaocheng P.R. China.
Food Sci Nutr. 2023 Mar 31;11(6):3550-3557. doi: 10.1002/fsn3.3343. eCollection 2023 Jun.
Small peptides can be absorbed by the bovine mammary gland for the synthesis of milk protein, but the absorption mechanism still needs further study. In this study, the role of peptide transporters in small peptide uptake by bovine mammary epithelial cells (BMECs) was studied. First, BMECs were obtained and cultured in a transwell chamber. After 5 days of culture, the FITC-dextran permeability of the cell layer was detected. Then, 0.5 mM methionyl-methionine (Met-Met) was added to the medium of the lower and upper transwell chambers, respectively. The culture medium and BMECs were collected after 24 h of treatment. Liquid chromatography-mass spectrometry (LC-MS) was used to detect the concentration of Met-Met in the culture medium. Real-time PCR was used to detect the mRNA abundance of β-casein, oligopeptide transporter 2 (PepT2), and small peptide histidine transporter 1 (PhT1) in BMECs. Then, the BMECs were transfected with siRNA-PepT2 and siRNA-PhT1, respectively, and the uptake of β-Ala-Lys-N-7-amino-4-methylcoumarin-3-acetic acid (β-Ala-Lys-AMCA) in BMECs was detected. The results showed that, after 5 days of culture, the FITC-dextran permeability of BMECs was 0.6%, which was significantly lower than that of the control group. The absorption rates of Met-Met in the culture medium of the upper and lower chambers were 99.99% and 99.95%, respectively. The addition of Met-Met to the upper chamber significantly increased the mRNA abundance of β-casein and PepT2. The addition of Met-Met to the lower chamber significantly improved the mRNA abundance of β-casein, PepT2, and PhT1. The uptake of β-Ala-Lys-AMCA significantly decreased in BMECs transfected with siRNA-PepT2. These results suggested that the BMECs were successfully cultured in the transwell chamber and formed a cell layer with little permeability. The small peptides in both the upper and lower chambers of the transwell can be absorbed by BMECs in different ways. PepT2 plays an important role in the uptake of small peptides on both the basal and apical sides of BMECs, and PhT1 may be involved in the uptake of small peptides on the basal side of BMECs. Therefore, the addition of small peptides in dairy cow diets may be an effective dietary manipulation to increase milk protein concentration or yield.
小肽可被牛乳腺吸收用于合成乳蛋白,但其吸收机制仍需进一步研究。本研究探讨了肽转运体在牛乳腺上皮细胞(BMECs)摄取小肽中的作用。首先,获取BMECs并在Transwell小室中培养。培养5天后,检测细胞层的FITC - 葡聚糖通透性。然后,分别在上下Transwell小室的培养基中添加0.5 mM的蛋氨酰 - 蛋氨酸(Met - Met)。处理24小时后收集培养基和BMECs。采用液相色谱 - 质谱联用(LC - MS)检测培养基中Met - Met的浓度。利用实时荧光定量PCR检测BMECs中β - 酪蛋白、寡肽转运体2(PepT2)和小肽组氨酸转运体1(PhT1)的mRNA丰度。接着,分别用siRNA - PepT2和siRNA - PhT1转染BMECs,并检测BMECs中β - 丙氨酰 - 赖氨酸 - N - 7 - 氨基 - 4 - 甲基香豆素 - 3 - 乙酸(β - Ala - Lys - AMCA)的摄取情况。结果显示,培养5天后,BMECs的FITC - 葡聚糖通透性为0.6%,显著低于对照组。上下室培养基中Met - Met的吸收率分别为99.99%和99.95%。向上室添加Met - Met显著增加了β - 酪蛋白和PepT2的mRNA丰度。向下室添加Met - Met显著提高了β - 酪蛋白、PepT2和PhT1的mRNA丰度。用siRNA - PepT2转染的BMECs中β - Ala - Lys - AMCA的摄取显著降低。这些结果表明,BMECs在Transwell小室中成功培养并形成了低通透性的细胞层。Transwell上下室中的小肽均可被BMECs以不同方式吸收。PepT2在BMECs的基底侧和顶端侧摄取小肽过程中起重要作用,PhT1可能参与BMECs基底侧小肽的摄取。因此,在奶牛日粮中添加小肽可能是提高乳蛋白浓度或产量的一种有效日粮调控方式。