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Protein expression of lymphocytes in HLA-DR transgenic pigs by a proteomic approach

机译:蛋白质组学方法在HLA-DR转基因猪中淋巴细胞的蛋白表达

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Matching donor and recipient human leucocyte antigen (HLA-II) could conquer cell-mediated rejection following transplantation. Transgenic pigs carrying HLA genes that "humanize" porcine organs, tissues, and cells were successfully generated. This study further clarifies the effect of HLA-DR transgenes on lymphocyte protein expression, via a proteomic approach. Lymphocytes were isolated from two HLA-DR transgenic pigs and three nontransgenic littermates on 157 d after birth. Soluble protein of 1 x 10(7) cells was separated using 2-DE. In total, 301 colloidal CBB-stained protein spots detected on all five 2-D gels were quantified. Thirty-three proteins were differentially expressed by a factor of 1.5. These proteins were subsequently identified by MALDI-TOF MS and MALDI-TOF/TOF MS/MS. These proteins were sorted into the following categories: chaperones, T-lymphocyte function, DNA/RNA processing, cytoskeleton-associated proteins, signal transduction, enzymes, and unknown. Previous studies have suggested that some of the identified proteins are associated with lymphocyte activation/proliferation. The identities of the unidentified spots and the systematic effect of these up- and down-regulated proteins on T-cell function in HLA-DR transgenic pigs require further exploration.
机译:匹配的供体和受体人类白细胞抗原(HLA-II)可以在移植后克服细胞介导的排斥反应。成功产生了带有“人性化”猪器官,组织和细胞的HLA基因的转基因猪。这项研究通过蛋白质组学方法进一步阐明了HLA-DR转基因对淋巴细胞蛋白质表达的影响。出生后157 d从两只HLA-DR转基因猪和三只非转基因同窝仔猪中分离出淋巴细胞。使用2-DE分离1 x 10(7)细胞的可溶性蛋白。总共对在所有5种2-D凝胶中检测到的301个CBB胶体蛋白斑点进行了定量分析。 33种蛋白质的差异表达系数为1.5。随后通过MALDI-TOF MS和MALDI-TOF / TOF MS / MS鉴定了这些蛋白质。这些蛋白质分为以下几类:分子伴侣,T淋巴细胞功能,DNA / RNA加工,细胞骨架相关蛋白,信号转导,酶和未知蛋白。先前的研究表明,某些鉴定出的蛋白质与淋巴细胞激活/增殖有关。这些尚未确定的斑点的身份以及这些上调和下调的蛋白对HLA-DR转基因猪T细胞功能的系统性影响需要进一步探索。

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