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Proteomic study of the establishment of boar epididymal cell cultures

机译:建立公猪附睾细胞培养物的蛋白质组学研究

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A proteomic approach was used in this study to follow the protein expression of epididymal cells during the different phases of a cell culture protocol which was able to obtain an epididymal cell monolayer. The secretory activity of intact proximal and middle caput epididymal fragments and caput, corpus and cauda epithelial cell monolayers was examined on different days of culture. Transcriptomic activity was also followed by RT-PCR for the mRNA of several previously identified major proteins. During the establishment of epididymal cell cultures, a progressive shift was found in the pattern of protein secretion. The normal epididymal protein profile, specific for each epididymal region, was progressively replaced by a less specific profile with the secretion of new proteins. A correlation between protein secretion and the presence of the mRNA of the marker proteins was observed only in the first phase of culture. Most of the new proteins which appeared were characteristic of the secretion of cell monolayers cultivated over several weeks. Despite the significant modifications of the epididymal cell secretome, the presence of new proteins secreted only by cell cultures originating from a specific epididymal region shows the presence of remaining endogenous differentiation.
机译:在这项研究中,采用蛋白质组学方法来跟踪附睾细胞的蛋白质表达,该过程在能够获得附睾细胞单层的细胞培养方案的不同阶段进行。在培养的不同天数检查完整的近端和中位附睾附睾片段以及帽,体和马尾上皮细胞单层的分泌活性。 RT-PCR还检测了一些先前鉴定出的主要蛋白质的mRNA的转录活性。在附睾细胞培养物的建立过程中,发现了蛋白质分泌模式的逐步转变。对每个附睾区域特异的正常附睾蛋白质谱逐渐被分泌新蛋白的次特异性谱所取代。仅在培养的第一阶段中观察到蛋白质分泌与标志物蛋白质的mRNA之间的相关性。出现的大多数新蛋白质是经过数周培养的细胞单层分泌物的特征。尽管附睾细胞分泌基因组进行了重大修饰,但仅由源自特定附睾区域的细胞培养物分泌的新蛋白质的存在表明仍存在内源性分化。

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