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Rumen fluid inhibits proliferation and stimulates expression of cyclin-dependent kinase inhibitors 1A and 2A in bovine rumen epithelial cells

机译:瘤胃液抑制牛瘤胃上皮细胞增殖并刺激细胞周期蛋白依赖性激酶抑制剂1A和2A的表达

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It has been known for decades that microbial fermentation within the rumen is critical to postnatal rumen epithelial growth and maturation in ruminants, but the underlying mechanism is largely unknown. In this study, we determined the effect of rumen fluid, which should contain all products from rumen fermentation, on growth of rumen epithelial cells in vitro. Addition of 10% rumen fluid from cows to the culture medium inhibited (P < 0.05), whereas addition of 6.5 mM acetate, 2.5 mM propionate, or 1 mM butyrate had no effect (P > 0.1) on, the proliferation of rumen epithelial cells isolated from newborn calves. Flow cytometric assays showed that 10% rumen fluid inhibited (P < 0.05) the transition of rumen epithelial cells from the G1 phase to the S phase during the cell cycle. Real-time RT-PCR analyses of mRNA for key cell cycle regulators indicated that 10% rumen fluid did not change (P > 0.1) the expression of cyclin D1, D2, D3, E1, or E2 mRNA or that of cyclin-dependent kinase inhibitor 1B or 2B mRNA, but increased (P < 0.05) the expression of cyclin-dependent kinase inhibitors 1A and 2A mRNA in rumen epithelial cells. These mRNA data support the possibility that rumen fluid inhibits proliferation of rumen epithelial cells in vitro by increasing the expression of cyclin-dependent kinase inhibitors 1A and 2A. The result that rumen fluid inhibits proliferation of bovine rumen epithelial cells in culture indicates that rumen fermentation does not stimulate the postnatal rumen epithelial growth in cattle by directly stimulating proliferation of rumen epithelial cells.
机译:数十年来,已知瘤胃内的微生物发酵对于产后瘤胃上皮瘤胃的生长和反刍动物的成熟至关重要,但其潜在机制尚不清楚。在这项研究中,我们确定了瘤胃液(其中应包含瘤胃发酵的所有产物)对瘤胃上皮细胞体外生长的影响。从牛中向培养基中添加10%的瘤胃液具有抑制作用(P <0.05),而添加6.5 mM乙酸盐,2.5 mM丙酸盐或1 mM丁酸盐对瘤胃上皮细胞的增殖没有影响(P> 0.1)。与新生小牛隔离。流式细胞仪检测表明,在细胞周期中,有10%的瘤胃液抑制了瘤胃上皮细胞从G1期到S期的转变(P <0.05)。对关键细胞周期调节因子的mRNA进行实时RT-PCR分析表明,10%的瘤胃液未改变(P> 0.1)cyclin D1,D2,D3,E1或E2 mRNA或细胞周期蛋白依赖性激酶的表达抑制因子1B或2B mRNA的表达,但瘤胃上皮细胞中细胞周期蛋白依赖性激酶抑制剂1A和2A mRNA的表达增加(P <0.05)。这些mRNA数据支持瘤胃液通过增加细胞周期蛋白依赖性激酶抑制剂1A和2A的表达在体外抑制瘤胃上皮细胞增殖的可能性。瘤胃液抑制培养物中牛瘤胃上皮细胞增殖的结果表明,瘤胃发酵不通过直接刺激瘤胃上皮细胞增殖来刺激牛的产后瘤胃上皮生长。

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