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The influence of technical factors on differential cell count in milk

机译:技术因素对牛奶中差异细胞计数的影响

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Differential cell count of milk is a traditional parameter for the evaluation of udder health. The literature shows great variation in differential cell counts of the milk of healthy mammary glands: macrophages range from 0% to 80%, lymphocytes from 1.5% to 79.5%, polymorpho-nuclear neutrophils from 3% to 95%, and epithelial cells from 1% to 19%. We conducted three studies to seek explanations for such variation. In the first, we evaluated the impact of polyethylene and glass sampling bottles. The aim of the second study was to compare the results of differential cell counts performed by three different technicians. The third study evaluated two methods of smear preparation. When polyethylene plastic bottles were used, the macrophage population was minimized but lymphocytes remained unaffected. This was shown by an exemplary flow cytometric analysis using four monoclonal antibodies against three lymphocyte surface structures. There were significant differences in the differential cell counts of 40 smears made by three technicians despite identical operating procedures. For the sediment smear, milk was centrifuged once and the sediment spread by eye on a glass slide. For the "coffee grinder" smear method, the sample was subjected to four centrifugations and then placed on a cover glass in order to spread the sediment using centrifugal force. The coffee grinder procedure led to a reduction of lymphocytes and an enrichment of polymorphonuclear neutrophils without affecting the macrophage population. Both methods made it possible to distinguish different udder health classes. It can be concluded that differential cell counts are a useful tool for comparing and monitoring udder health only if: samples are taken in a glass bottle; smears are prepared with the identical technique; and the differential cell counts are performed by a single person.
机译:牛奶的差异细胞计数是评估乳房健康的传统参数。文献显示,健康乳腺的乳腺细胞差异很大:巨噬细胞范围从0%到80%,淋巴细胞范围从1.5%到79.5%,多形核中性粒细胞从3%到95%,上皮细胞从1 %至19%。我们进行了三项研究,以寻求对此变化的解释。首先,我们评估了聚乙烯和玻璃采样瓶的影响。第二项研究的目的是比较由三名不同技术人员执行的差分细胞计数结果。第三项研究评估了两种涂片准备方法。当使用聚乙烯塑料瓶时,巨噬细胞的数量减至最小,但淋巴细胞不受影响。通过使用针对三种淋巴细胞表面结构的四种单克隆抗体的示例性流式细胞术分析表明了这一点。尽管操作步骤相同,但三名技术人员进行的40次涂片的细胞计数差异显着。对于沉淀物涂片,将牛奶离心一次,然后将沉淀物通过肉眼在载玻片上散布。对于“咖啡研磨机”涂片方法,将样品进行四次离心分离,然后置于盖玻片上,以便利用离心力分散沉积物。咖啡研磨器程序导致淋巴细胞减少和多形核中性粒细胞的富集,而不影响巨噬细胞的数量。两种方法都可以区分不同的乳房健康等级。可以得出结论,只有在以下情况下,差异细胞计数才是比较和监测乳房健康的有用工具:涂片用相同的技术准备;差分细胞计数由一个人执行。

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