首页> 外文期刊>Biological trace element research >Manganese regulates manganese-containing superoxide dismutase (MnSOD) expression in the primary broiler myocardial cells.
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Manganese regulates manganese-containing superoxide dismutase (MnSOD) expression in the primary broiler myocardial cells.

机译:锰调节初级肉鸡心肌细胞中含锰的超氧化物歧化酶(MnSOD)的表达。

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摘要

Previous studies showed that dietary manganese can increase the MnSOD mRNA expression in a dose-dependent manner in the heart of broilers. In order to explore the specific mechanism of the MnSOD expression induced by manganese, a model of MnSOD expression was developed with primary cultured broiler myocardial cells. The objective of the present study was to investigate whether the model was working or not and to determine how manganese affects the expression of the enzyme in broiler myocardial cells in vitro. In experiment 1, various amount of manganese (0, 0.25, 0.5, 1, 2, and 4 mM) were added into the cultures for 24-h incubation to investigate MnSOD expression and for 0-, 6-, 12-, 24-, 36-, and 48-h incubation to measure the cell viability. In experiment 2, the most suitable Mn supplementation based on the results of experiment 1 was added into cultures for 6-, 12-, 24-, and 48-h incubation. The results showed that MnSOD mRNA, MnSOD protein, and MnSOD activity were induced by manganese in dose- and time-dependent manner. Manganese regulates MnSOD expression not only at transcriptional level but also at translational and/or posttranslational levels.
机译:先前的研究表明,膳食锰可以在肉鸡心脏中以剂量依赖的方式增加MnSOD mRNA的表达。为了探索锰诱导的MnSOD表达的具体机制,建立了以原代培养的肉鸡心肌细胞为模型的MnSOD表达模型。本研究的目的是研究该模型是否有效,并确定锰如何在体外影响肉鸡心肌细胞中酶的表达。在实验1中,将各种量的锰(0、0.25、0.5、1、2和4 mM)添加到培养物中进行24小时孵育以研究MnSOD的表达以及0、6、12、24和24 ,36和48小时的孵育时间以测量细胞活力。在实验2中,根据实验1的结果,将最合适的Mn添加到培养物中进行6、12、24和48小时的培养。结果表明,锰以剂量和时间依赖性方式诱导了MnSOD mRNA,MnSOD蛋白和MnSOD的活性。锰不仅在转录水平而且在翻译水平和/或翻译后水平调节MnSOD表达。

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