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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Differential expression of alpha-GAL epitopes (Galalpha1-3Galbeta1-4GlcNAc-R) on pig and mouse organs.
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Differential expression of alpha-GAL epitopes (Galalpha1-3Galbeta1-4GlcNAc-R) on pig and mouse organs.

机译:猪和小鼠器官上的alpha-GAL表位(Galalpha1-3Galbeta1-4GlcNAc-R)的差异表达。

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BACKGROUND: Expression of the alpha-gal epitope in mice can be completely eliminated by disruption of the alpha1,3 galactosyltransferase gene. As an initial step for assessing the feasibility of this approach in the pig, it was of interest to compare the expression of alpha-gal epitopes in pig and mouse organs. METHODS: Membranes from pig and mouse organ homogenates were analyzed for alpha-gal epitope expression by Western blots, enzyme-linked immunosorbent assay (ELISA), immunostaining of tissues, and ELISA inhibition assay. RESULTS: Immunostaining of Western blots with human anti-Gal detected alpha-gal epitopes on glycoproteins from pig organs but not on glycoproteins from the corresponding mouse organs. ELISA with membrane homogenates and immunostaining of tissue sections demonstrated a much higher binding of human anti-Gal to alpha-gal epitopes on pig membranes than on mouse membranes. ELISA inhibition assay with monoclonal anti-Gal indicated that alpha-gal epitope expression in pig organs is up to 500-fold higher than in mouse organs. CONCLUSION: Expression of alpha-gal epitopes in pig organs is many fold higher than in mouse organs. The abundance of these epitopes in pigs raises the question of whether pigs can properly develop without expression of alpha-gal epitopes.
机译:背景:通过破坏α1,3半乳糖基转移酶基因可以完全消除小鼠中的α-gal表位。作为评估这种方法在猪中的可行性的第一步,比较猪和小鼠器官中α-gal表位的表达很有意义。方法:通过Western印迹,酶联免疫吸附测定(ELISA),组织免疫染色和ELISA抑制测定分析猪和小鼠器官匀浆的膜的α-gal表位表达。结果:用人抗-Gal免疫印迹法检测了猪器官糖蛋白上的α-gal表位,但未检测到相应小鼠器官糖蛋白上的α-gal表位。带有膜匀浆的ELISA和组织切片的免疫染色证明,人抗-Gal与猪膜上的α-gal表位的结合远高于小鼠膜上的结合。用单克隆抗-Gal进行的ELISA抑制试验表明,猪器官中的α-gal表位表达比小鼠器官中的表达高500倍。结论:猪内脏器官中α-gal抗原决定簇的表达比小鼠内脏器官高很多倍。猪中这些表位的丰富性提出了一个问题,即在不表达α-gal表位的情况下猪是否可以正常发育。

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