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家蚕胚胎细胞系的无血清培养及重组 BmNPV 通过降温增强其敏感性。

Serum-free culture of an embryonic cell line from Bombyx mori and reinforcement of susceptibility of a recombinant BmNPV by cooling.

机构信息

Department of Insect Science, National Institute of Agrobiological Sciences, Ibaraki, Japan.

出版信息

In Vitro Cell Dev Biol Anim. 2012 Mar;48(3):137-42. doi: 10.1007/s11626-011-9465-9.

Abstract

We established the first continuous cell line that uses a serum-free culture from the embryo of Bombyx mori (Lepidoptera: Bombycidae), designated as NIAS-Bm-Ke17. This cell line was serially subcultured in the SH-Ke-117 medium. The cells adhere weakly to the culture flask, and most cells have an oval shape. The cell line was subcultured 154 times, and the population doubling time is 83.67±5.22 h. Random amplification of polymorphic DNA-polymerase chain reaction with a tenmar single primer for discrimination of insect cell lines recognized the NIAS-Bm-Ke1 cell line as B. mori. This cell line does not support the growth of the B. mori nuclear polyhedrosis virus (BmNPV) in the absence of the heat-inactivated hemolymph of B. mori. However, the heat-inactivated hemolymph in 1% volume of the medium supported a high level of susceptibility to BmNPV. In addition, the cooling treatment of the cells at 2.5°C also enhanced the susceptibility. We report a new serum-free culture system of the B. mori cell line for the baculovirus expression vector system.

摘要

我们建立了第一个使用家蚕(鳞翅目:天蚕科)胚胎无血清培养的连续细胞系,命名为 NIAS-Bm-Ke17。该细胞系在 SH-Ke-117 培养基中连续传代培养。细胞弱贴附于培养瓶,多数细胞呈椭圆形。该细胞系已传代 154 次,群体倍增时间为 83.67±5.22 h。用单引物 tenmar 随机扩增多态性 DNA-聚合酶链反应鉴定昆虫细胞系,NIAS-Bm-Ke1 细胞系被识别为家蚕。该细胞系在缺乏家蚕热失活血淋巴的情况下,不支持家蚕核多角体病毒(BmNPV)的生长。然而,培养基中 1%体积的热失活血淋巴支持对 BmNPV 的高敏感性。此外,细胞在 2.5°C 的冷却处理也增强了敏感性。我们报告了一种新的家蚕细胞系无血清培养系统,用于杆状病毒表达载体系统。

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