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bcl-2 在 Spodoptera Frugiperda Sf-9 和 Trichoplusia Ni BTI-Tn-5B1-4 昆虫细胞中的表达:对重组蛋白表达和细胞活力的影响。

bcl-2 expression in Spodoptera Frugiperda Sf-9 and Trichoplusia Ni BTI-Tn-5B1-4 insect cells: effect on recombinant protein expression and cell viability.

机构信息

Department of Chemical and Biochemical Engineering, The University of Iowa, Iowa City, IA 52242-1219, USA.

出版信息

Biotechnol Bioeng. 1997 Nov 20;56(4):380-90. doi: 10.1002/(SICI)1097-0290(19971120)56:4<380::AID-BIT4>3.0.CO;2-K.

Abstract

The effect of bcl-2 expression on cell viability and recombinant protein synthesis was investigated in the Spodoptera frugiperda Sf-9 and Trichoplusia ni BTI-Tn-5B1-4 (High Fivetrade mark) insect cell lines. It was found that coinfection with a baculovirus expressing bcl-2 [Autographa californica nuclear polyhedrosis virus (AcNPV)-bcl2] extended the life span of High Fivetrade mark cells but not Sf-9 cells when compared to infection with recombinant baculoviruses expressing either human tissue plasminogen activator (AcNPV-tPA) or Escherichia coli beta-galactosidase (AcNPV-betagal). Similar results were obtained in coinfection experiments; i.e., AcNPV-bcl2 coinfection increased the life span of High Fivetrade mark cells over that of cells infected with either AcNPV-tPA or AcNPV-betagal alone, but they did not affect the life span of coinfected Sf-9 cells. Coinfection of Sf-9 cells with AcNPV-bcl2 and AcNPV-betagal resulted in a decrease in the maximum beta-gal expression levels of over 90% when compared to infection with AcNPV-betagal alone. A similar trend was found in the beta-gal mRNA levels. Coinfection also resulted in a reduced beta-gal expression level in High Fivetrade mark cells, but the reduction was consistent with what would be expected when two recombinant viruses compete for use of the cellular machinery. In contrast to the inhibitory effect of AcNPV-bcl2 coinfection on betagal expression, t-PA expression levels were either not affected (Sf-9 cells) or were increased 50% (High Fivetrade mark cells) over those obtained by infection with AcNPV-tPA alone. These results support the hypotheses that bcl-2 can inhibit transcription of genes under polyhedrin promoter control and that beta-gal expression levels, but not t-PA expression levels, are controlled at the transcriptional level. (c) 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 56: 380-390, 1997.

摘要

在草地贪夜蛾 Sf-9 和三化螟 BTI-Tn-5B1-4(High FiveTM 商标)昆虫细胞系中研究了 bcl-2 表达对细胞活力和重组蛋白合成的影响。结果发现,与感染表达人组织纤溶酶原激活物(AcNPV-tPA)或大肠杆菌β-半乳糖苷酶(AcNPV-betagal)的重组杆状病毒相比,共感染表达 bcl-2 的杆状病毒[Autographa californica 核多角体病毒(AcNPV)-bcl2]可延长 High FiveTM 商标细胞的寿命,但不能延长 Sf-9 细胞的寿命。在共感染实验中也得到了类似的结果;即 AcNPV-bcl2 共感染可延长 High FiveTM 商标细胞的寿命,超过单独感染 AcNPV-tPA 或 AcNPV-betagal 的细胞,但不影响共感染 Sf-9 细胞的寿命。与单独感染 AcNPV-betagal 相比,Sf-9 细胞共感染 AcNPV-bcl2 和 AcNPV-betagal 导致β-半乳糖苷酶的最大表达水平降低了 90%以上。在β-半乳糖苷 mRNA 水平上也发现了类似的趋势。共感染还导致 High FiveTM 商标细胞的β-半乳糖苷表达水平降低,但这种降低与两种重组病毒竞争使用细胞机制时的预期一致。与 AcNPV-bcl2 共感染对 betagal 表达的抑制作用相反,t-PA 表达水平要么不受影响(Sf-9 细胞),要么比单独感染 AcNPV-tPA 时增加 50%(High FiveTM 商标细胞)。这些结果支持以下假设:bcl-2 可以抑制多角体启动子控制下基因的转录,并且β-半乳糖苷表达水平,而不是 t-PA 表达水平,受转录水平控制。(c)1997 年 John Wiley & Sons,Inc. 生物技术与生物工程 56:380-390,1997 年。

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