Jaswal Shalini, Anand Vijay, Ali Syed Azmal, Jena Manoj K, Kumar Sudarshan, Kaushik Jai K, Mohanty Ashok K
Proteomics and Cell Biology Lab, Animal Biotechnology Centre, National Dairy Research Institute (NDRI), Karnal, India.
Department of Veterinary Physiology and Biochemistry, Veterinary College and Research Institute (TANUVAS), Orathanadu, India.
FASEB J. 2021 Jun;35(6):e21621. doi: 10.1096/fj.202002476RR.
The lactating mammary gland harbours numerous matured alveoli with their lumen surrounded by differentiated mammary epithelial cells (MECs), which are exclusively involved in milk synthesis and secretion. Buffalo (Bubalus bubalis) is the second major milk-producing animal, and its physiology is different from cattle. The complete protein machinery involved in MECs differentiation is still not defined in ruminants, in particular, buffalo. Therefore, we have studied the differential expression of regulated proteins in the in vitro grown buffalo MECs (BuMECs) at different time points (on 3, 6, 12, and 15 days) of their differentiation in the presence of lactogenic hormones. TMT-based MS analysis identified 4,934 proteins; of them, 681 were differentially expressed proteins (DEPs). The principal component analysis suggested a highly heterogeneous expression of DEPs at the four-time points of hormone treatment, with most of them (307) attained the highest expression on 12 days. Bioinformatics analysis revealed the association of DEPs with 24 KEGG pathways. We observed few new proteins, namely ABCA13, IVL, VPS37, CZIB, RFX7, Rab5, TTLL12, SMEK1, GDI2, and TMEM131 in BuMECs. The function of one of the highly upregulated proteins, namely involucrin in the differentiation of BuMECs was confirmed based on biochemical inhibition assay. The results further conclude that the proteins with higher abundance can be considered as the potential biomarkers for differentiation, and they may have a significant association with the lactation process in buffalo too. The proteome dataset obtained can be used to understand the species-specific variations among other lactating animals.
泌乳期乳腺含有大量成熟的腺泡,其管腔被分化的乳腺上皮细胞(MECs)包围,这些细胞专门参与乳汁的合成和分泌。水牛(Bubalus bubalis)是第二大主要产奶动物,其生理机能与牛不同。反刍动物,尤其是水牛,参与MECs分化的完整蛋白质机制仍未明确。因此,我们研究了在体外培养的水牛MECs(BuMECs)中,在泌乳激素存在的情况下,其分化不同时间点(第3、6、12和15天)调控蛋白的差异表达。基于TMT的质谱分析鉴定出4934种蛋白质;其中,681种为差异表达蛋白(DEPs)。主成分分析表明,在激素处理的四个时间点,DEPs的表达高度异质,其中大多数(307种)在第12天达到最高表达。生物信息学分析揭示了DEPs与24条KEGG通路的关联。我们在BuMECs中观察到一些新蛋白质,即ABCA13、IVL、VPS37、CZIB、RFX7、Rab5、TTLL12、SMEK1、GDI2和TMEM131。基于生化抑制试验证实了高度上调的蛋白质之一——内披蛋白在BuMECs分化中的功能。结果进一步表明,丰度较高的蛋白质可被视为分化的潜在生物标志物,它们可能也与水牛的泌乳过程有显著关联。获得的蛋白质组数据集可用于了解其他泌乳动物之间的物种特异性差异。