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在转染了CD59的中国仓鼠卵巢细胞中,基因表达增强赋予了对人补体膜攻击复合物的抗性。

Amplified gene expression in CD59-transfected Chinese hamster ovary cells confers protection against the membrane attack complex of human complement.

作者信息

Zhao J, Rollins S A, Maher S E, Bothwell A L, Sims P J

机构信息

Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City 73104.

出版信息

J Biol Chem. 1991 Jul 15;266(20):13418-22.

PMID:1712784
Abstract

Protection against the pore-forming activity of the human C5b-9 proteins was conferred on a nonprimate cell by transfection with cDNA encoding the human complement regulatory protein CD59. CD59 was stably expressed in Chinese hamster ovary cells using the pFRSV mammalian expression vector. After cloning and selection, the transfected cells were maintained in media containing various concentrations of methotrexate, which induced surface expression of up to 4.2 x 10(6) molecules of CD59/cell. Phosphatidylinositol-specific phospholipase C removed greater than 95% of surface-expressed CD59 antigen, confirming that recombinant CD59 was tethered to the Chinese hamster ovary plasma membrane by a lipid anchor. The recombinant protein exhibited an apparent molecular mass of 21-24 kDa (versus 18-21 kDa for human erythrocyte CD59). After N-glycanase digestion, recombinant and erythrocyte CD59 comigrated with apparent molecular masses of 12-14 kDa, suggesting altered structure of asparagine-linked carbohydrate in recombinant versus erythrocyte CD59. The function of the recombinant protein was evaluated by changes in the sensitivity of the CD59 transfectants to the pore-forming activity of human C5b-9. Induction of cell-surface expression of CD59 antigen inhibited C5b-9 pore formation in a dose-dependent fashion. CD59 transfectants expressing greater than or equal to 1.2 x 10(6) molecules of CD59/cell were completely resistant to human serum complement. By contrast, CD59 transfectants remained sensitive to the pore-forming activity of guinea pig C8 and C9 (bound to human C5b67). Functionally blocking antibody against erythrocyte CD59 abolished the human complement resistance observed for the CD59-transfected Chinese hamster ovary cells. These results confirm that the C5b-9 inhibitory function of the human erythrocyte membrane is provided by CD59 and suggest that the gene for this protein can be expressed in xenotypic cells to confer protection against human serum complement.

摘要

通过转染编码人补体调节蛋白CD59的cDNA,非灵长类细胞获得了针对人C5b - 9蛋白成孔活性的保护作用。使用pFRSV哺乳动物表达载体,CD59在中国仓鼠卵巢细胞中稳定表达。经过克隆和筛选后,将转染细胞培养在含有不同浓度甲氨蝶呤的培养基中,可诱导细胞表面表达高达4.2×10⁶个CD59分子/细胞。磷脂酰肌醇特异性磷脂酶C去除了超过95%的表面表达的CD59抗原,证实重组CD59通过脂质锚定连接到中国仓鼠卵巢细胞质膜上。重组蛋白的表观分子量为21 - 24 kDa(而人红细胞CD59为18 - 21 kDa)。经N - 糖苷酶消化后,重组CD59和红细胞CD59的表观分子量均为12 - 14 kDa,提示重组CD59与红细胞CD59中天冬酰胺连接的碳水化合物结构有所改变。通过检测CD59转染细胞对人C5b - 9成孔活性敏感性的变化来评估重组蛋白的功能。CD59抗原的细胞表面表达诱导以剂量依赖性方式抑制C5b - 9孔形成。表达≥1.2×10⁶个CD59分子/细胞的CD59转染细胞对人血清补体完全抗性。相比之下,CD59转染细胞对豚鼠C8和C9(与人C5b67结合)的成孔活性仍敏感。针对红细胞CD59的功能阻断抗体消除了CD59转染的中国仓鼠卵巢细胞所观察到的人补体抗性。这些结果证实人红细胞膜的C5b - 9抑制功能由CD59提供,并提示该蛋白基因可在异种细胞中表达以赋予对人血清补体的保护作用。

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