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使用一次性固定床生物反应器进行昆虫细胞包埋、生长及回收。放大培养及重组蛋白生产。

Insect cell entrapment, growth and recovering using a single-use fixed-bed bioreactor. Scaling up and recombinant protein production.

作者信息

Ventini-Monteiro D, Dubois S, Astray R M, Castillo J, Pereira C A

机构信息

Instituto Butantan, Laboratório de Imunologia Viral, Av. Vital Brasil 1500, 05503-900 São Paulo, Brazil; Universidade de São Paulo, Escola Politécnica, Departamento de Engenharia Química, Laboratório de Células Animais, Av. Prof. Luciano Gualberto 380, 05508-900 São Paulo, Brazil.

Pall Life Science/ATMI/Artelis, rue de Ransbeek 310, 1120 Brussels, Belgium.

出版信息

J Biotechnol. 2015 Dec 20;216:110-5. doi: 10.1016/j.jbiotec.2015.10.013. Epub 2015 Oct 23.

Abstract

Insect cells are largely used for industrial production of vaccines, viral vectors and recombinant proteins as well as in research and development as an important tool for biology and bioprocess studies. They grow in suspension and are semi-adherent cells. Among the cell culture systems enabling scalable bioprocess the single-use fixed-bed iCELLis(®) bioreactors offer great advantages. We have established the conditions for Drosophila melanogaster Schneider 2 (S2) and Spodoptera frugiperda (Sf9) cells entrapment into the fixed-bed, cell growth and recover from the fixed-bed once high cell densities were attained. Our established protocol allowed these cells, at a cell seeding of 2×1E5 cells/microfiber carriers (MC) (3.5×1E6cells/mL; 1.7×1E4cells/cm(2)), to grow inside a 4m(2)/200mL fixed-bed attaining a concentration of 5.3×1E6 cells/MC (9.5×1E7cells/mL; 4.7×1E5 cells/cm(2)) for S2 cells or 4.6×1E6 cells/MC (8×1E7cells/mL; 4.1×1E5cells/cm(2)) for Sf9 cells. By washing the fixed-bed, entrapped cells could then be recovered from the fixed-bed at a high rate (>85%) with high viability (>95%) by increasing the agitation to 1200/1500rpm. Although the cell yields in the fixed-bed bioreactor were comparable to those obtained in a stirred tank (respectively, 1.3×1E10 and 2.5×1E10 total cells), S2 cells stably transfected with a cDNA coding for the rabies virus glycoprotein (RVGP) showed a 30% higher preserved rRVGP production (2.5±0.1 and 1.9±0.1μg/1E7 cells), as evidenced by a conformational ELISA evaluation. These findings demonstrate not only the possibility to entrap, cultivate to high densities and recover insect cells using a single-use fixed-bed bioreactor, but also that this system provides suitable physiological conditions for the entrapped cells to produce a cell membrane associated recombinant protein with higher specific biological activity as compared to classical suspension cell cultures.

摘要

昆虫细胞在很大程度上被用于疫苗、病毒载体和重组蛋白的工业生产,以及作为生物学和生物工艺研究的重要工具用于研发。它们以悬浮形式生长,属于半贴壁细胞。在能够实现可扩展生物工艺的细胞培养系统中,一次性固定床iCELLis(®)生物反应器具有很大优势。我们已经确立了将黑腹果蝇施耐德2(S2)细胞和草地贪夜蛾(Sf9)细胞包埋到固定床中的条件、细胞生长条件以及在达到高细胞密度后从固定床中回收细胞的条件。我们既定的方案允许这些细胞以2×10⁵个细胞/微纤维载体(MC)(3.5×10⁶个细胞/毫升;1.7×10⁴个细胞/平方厘米)的细胞接种密度,在一个4平方米/200毫升的固定床内生长,S2细胞达到5.3×10⁶个细胞/MC(9.5×10⁷个细胞/毫升;4.7×10⁵个细胞/平方厘米) 的浓度,Sf9细胞达到4.6×10⁶个细胞/MC(8×10⁷个细胞/毫升;4.1×10⁵个细胞/平方厘米)的浓度。通过洗涤固定床,然后将搅拌速度提高到1200/1500转/分钟,就可以从固定床中以高回收率(>85%)和高活力(>95%)回收包埋的细胞。尽管固定床生物反应器中的细胞产量与搅拌罐中的相当(分别为1.3×10¹⁰和2.5×10¹⁰个总细胞),但用编码狂犬病病毒糖蛋白(RVGP)的cDNA稳定转染的S2细胞,经构象ELISA评估显示,其保留的重组狂犬病病毒糖蛋白(rRVGP)产量高30%(分别为2.5±0.1和1.9±0.1微克/10⁷个细胞)。这些发现不仅证明了使用一次性固定床生物反应器包埋、高密度培养和回收昆虫细胞的可能性,还证明了该系统为包埋的细胞提供了合适的生理条件,使其能够产生与经典悬浮细胞培养相比具有更高比生物活性的细胞膜相关重组蛋白。

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