RNAi介导的Bip表达下调促进基于蛋白质剪接的双链共转基因细胞分泌FVIII凝血活性

朱甫祥;刘泽隆;缪静;屈慧鸽;迟晓艳

解剖学报 ›› 2012, Vol. 43 ›› Issue (5) : 624-628.

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解剖学报 ›› 2012, Vol. 43 ›› Issue (5) : 624-628. DOI: 10.3969/j.issn.0529-1356.2012.05.008
细胞和分子生物学

RNAi介导的Bip表达下调促进基于蛋白质剪接的双链共转基因细胞分泌FVIII凝血活性

  • 朱甫祥*; 刘泽隆; 缪静; 屈慧鸽; 迟晓艳
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RNAi-mediated Bip knockdown improves secretion of FVIII activity by protein splicing-based two-chain gene transduced cells

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Abstract

Objective To investigate the effect of RNA Interfering-mediated down -regulation ER chaperon protein, immunoglobulin heavy-chain binding protein (Bip) on secretion of spliced FVIII and bioactivity from protein splicing based two-chain co-transgenic HEK293 cell. Methods After treatment with Bip-siRNA, the HEK293 cells were co-transfected with intein-contained B-domain-deleted FVIII(BDD-FVIII) heavy and light chain genes. The expression of Bip was observed by Western blotting with the cell growth atatus assayed by MTT. The quantitative secretion of spliced BDD-FVIII protein and bioactivity were measured by ELISA and coatest chromogenic method respectively. Results Bip was obviously down-regulated by RNA interference technonogy but with no effect on the cell proliferation. It showed a great higher level of spliced BDD-FVIII and heavy chain in terms of secretion by Bip-downregulated co-transgenic cell [(142±33)μg/L and (197±43)μg/L] compared to control[(89±23)μg/L and (120±27)μg/L]. The FVIII bioactivity in cell culture supernatant showed an elevated levels in Bip-downregulated co-transgenic cell [(1.05±0.16)IU/mL], greater than that of control [(0.64±0.17)IU/mL]. Co

关键词

凝血因子VIII / 免疫球蛋白重链结合蛋白 / 蛋白质剪接 / 双链转基因 / 免疫印迹法 / 酶联免疫吸附测定 / 发色分析法

Key words

Coagulation factor VIII / Bip / Protein splicing / Two-chain gene transfer / Western blotting / Enzyme-linked immunosorbent assay / Cotest chromogenic method

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朱甫祥;刘泽隆;缪静;屈慧鸽;迟晓艳. RNAi介导的Bip表达下调促进基于蛋白质剪接的双链共转基因细胞分泌FVIII凝血活性[J]. 解剖学报. 2012, 43(5): 624-628 https://doi.org/10.3969/j.issn.0529-1356.2012.05.008
RNAi-mediated Bip knockdown improves secretion of FVIII activity by protein splicing-based two-chain gene transduced cells[J]. Acta Anatomica Sinica. 2012, 43(5): 624-628 https://doi.org/10.3969/j.issn.0529-1356.2012.05.008
中图分类号: Q51    R96   

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