Shu Shi, Bai Yunlong, Wang Gang, Xiao Xinhuan, Fan Ziling, Zhang Jiang, Zhao Chang, Zhao Yang, Xia Cheng, Zhang Hongyou
College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Asian-Australas J Anim Sci. 2017 Jun;30(6):893-901. doi: 10.5713/ajas.16.0615. Epub 2016 Nov 3.
Hypocalcemia is an important metabolic disease of dairy cows during the transition period, although the effect of hypocalcemia on biological function in dairy cows remains unknown.
In this study, proteomic, mass spectrum, bioinformatics and western blotting were employed to identify differentially expressed proteins related to serum Ca concentration. Serum samples from dairy cows were collected at three time points: 3rd days before calving (day -3), the day of calving (day 0), and 3rd days after calving (day +3). According to the Ca concentration on day 0, a total of 27 dairy cows were assigned to one of three groups (clinical, subclinical, and healthy). Samples collected on day -3 were used for discovery of differentially expressed proteins, which were separated and identified via proteomic analysis and mass spectrometry. Bioinformatics analysis was performed to determine the function of the identified proteins (gene ontology and pathway analysis). The differentially expressed proteins were verified by western blot analysis.
There were 57 differential spots separated and eight different proteins were identified. Vitamin D-binding protein precursor (group-specific component, GC), alpha-2-macroglobulin (A2M) protein, and apolipoprotein A-IV were related to hypocalcemia by bioinformatics analysis. Due to its specific expression (up-regulated in clinical hypocalcemia and down-regulated in subclinical hypocalcemia), A2M was selected for validation. The results were consistent with those of proteomic analysis.
A2M was as an early detection index for distinguishing clinical and subclinical hypocalcemia. The possible pathogenesis of clinical hypocalcemia caused by GC and apolipoprotein A-IV was speculated. The down-regulated expression of GC was a probable cause of the decrease in calcium concentration.
低钙血症是奶牛围产期一种重要的代谢性疾病,但其对奶牛生物学功能的影响尚不清楚。
本研究采用蛋白质组学、质谱分析、生物信息学和蛋白质免疫印迹法,鉴定与血清钙浓度相关的差异表达蛋白。在三个时间点采集奶牛血清样本:产犊前3天(-3天)、产犊当天(0天)和产犊后3天(+3天)。根据0天的钙浓度,将27头奶牛分为三组(临床型、亚临床型和健康型)。采集-3天的样本用于差异表达蛋白的发现,通过蛋白质组学分析和质谱法进行分离和鉴定。进行生物信息学分析以确定所鉴定蛋白质的功能(基因本体论和通路分析)。通过蛋白质免疫印迹分析验证差异表达蛋白。
分离出57个差异点,鉴定出8种不同蛋白质。通过生物信息学分析,维生素D结合蛋白前体(组特异性成分,GC)、α-2-巨球蛋白(A2M)蛋白和载脂蛋白A-IV与低钙血症相关。由于其特异性表达(在临床低钙血症中上调,在亚临床低钙血症中下调),选择A2M进行验证。结果与蛋白质组学分析一致。
A2M可作为区分临床和亚临床低钙血症的早期检测指标。推测了由GC和载脂蛋白A-IV引起临床低钙血症的可能发病机制。GC表达下调可能是钙浓度降低的原因。