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Milk somatic cells are not suitable biomarkers of lactating ruminant mammary gland function

机译:牛奶体细胞不是哺乳反刍动物乳腺功能的合适生物标志物

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Understanding the molecular regulation of milk production by the ruminant mammary gland may help farmers meet increasing production milestones. Investigating these mechanisms currently relies upon invasive sampling by post-mortem or biopsy. The objective of this study was to determine if milk somatic cells, shed by the gland during milking, could be used as a non-invasive source of cells to measure these mechanisms. To answer this we employed two widely used molecular techniques, biochemical indicesand quantitative polymerase chain reaction (qPCR). Experiment 1: Biochemical indices as measures of cell size, protein production capacity and efficiency were determined in milk somatic cells and mammary tissue harvested from six lactating dairy goats. Results showed protein production capacity (P = 0.03) and cell size (P = 0.03) were higher in mammary tissue compared to somatic cells while protein production efficiency was unaffected (P = 0.55). Experiment 2: Milk protein and ribosomal RNA gene expression were measured using qPCR in milk somatic cells and mammary tissue collected from three lactating dairy cows treated with growth hormone and four treated with saline. Results showed expression of all genes differed between milk somatic cells and mammary tissue. Taken together, these results indicate milk somatic cells are not suitable for measuring biochemical indices or gene expression in the lactating ruminant mammary gland.
机译:了解反刍动物乳腺的牛奶产量的分子调控可能有助于农民符合增加的生产里程碑。调查这些机制目前依赖于验尸或活组织检查的侵入性取样。本研究的目的是确定挤奶过程中腺体脱落的牛奶体细胞,可用作衡量这些机制的非侵入性细胞来源。为了回答这一点,我们采用了两种广泛使用的分子技术,生物化学指数和定量聚合酶链反应(QPCR)。实验1:生物化学指数作为细胞尺寸的措施,蛋白质生产能力和效率测定,牛奶体细胞和哺乳奶牛收获的乳腺组织中。结果显示蛋白质生产能力(p = 0.03)和乳腺组织中的细胞尺寸(p = 0.03)与体细胞相比较高,而蛋白质生产效率不受影响(p = 0.55)。实验2:使用乳蛋白和核糖体RNA基因表达在用牛奶体细胞和用生长激素处理的三个哺乳奶牛组收集的乳腺细胞和乳腺组织测量,并用盐水处理。结果表明,乳细胞和乳腺组织之间的所有基因的表达。总之,这些结果表明牛奶体细胞不适合测量哺乳反刍动物乳腺中的生物化学指数或基因表达。

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