首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >A new continuous cell line from larval ovaries of silkworm, Bombyx mori
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A new continuous cell line from larval ovaries of silkworm, Bombyx mori

机译:家蚕幼虫卵巢的新连续细胞系

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A new continuous cell line from ovarian tissue of commercial variety Kolar Gold of silkworm, Bombyx mori, was established and designated as DZNU-Bm-12. The tissue was grown in MGM-448 insect cell culture medium supplemented with 10% fetal bovine serum (FBS) and 3% heat-inactivated B. mori hemolymph at 25 pl 1pC. The migration of partially attached small round refractive cells from the fragments of ovarioles began from the beginning of explantation. The cells multiplied partially attached in the primary culture initially, and some of them become freely suspended after 20 passages. The cells were adapted to MGM-448 and TNM-FH media each with 10% FBS and the population doubling time of cell line was about 36 and 24 hr, respectively. The chromosome number was near diploid at initial passages and slightly increased at 176th passage, but a few tetraploids and hexaploids were also observed. DNA profiles using simple sequence repeat loci established the differences between DZNU-Bm-12 and DZNU-Bm-1 and most widely used Bm-5 and BmN cell lines. The cell line was found susceptible to B. mori nucleopolyhedrovirus (BmNPV) with 85-90% of the cells harboring BmNPV and having an average of 3-17 OBs/infected cell. We suggest the usefulness of this cell line in BmNPV-based baculoviral expression system and also for studying in vitro virus replication.
机译:建立了来自商业变种蚕Kolar Gold的卵巢组织的新连续细胞系,家蚕,并命名为DZNU-Bm-12。使该组织在补充有10%胎牛血清(FBS)和3%热灭活的家蚕B.淋巴液的MGM-448昆虫细胞培养基中生长,浓度为25 pl 1pC。从附睾开始,部分附着的小圆形屈光细胞从卵泡的迁移开始。最初,细胞在原始培养物中部分增殖,部分细胞在传代20次后自由悬浮。使细胞适应各自具有10%FBS的MGM-448和TNM-FH培养基,并且细胞系的群体倍增时间分别为约36和24小时。染色体数目在最初的传代时接近二倍体,在第176传代时略有增加,但是也观察到一些四倍体和六倍体。使用简单的序列重复基因座的DNA图谱确定了DZNU-Bm-12和DZNU-Bm-1与最广泛使用的Bm-5和BmN细胞系之间的差异。发现该细胞系对桑蚕核多角体病毒(BmNPV)敏感,其中85-90%的细胞带有BmNPV,平均每感染细胞有3-17个OB。我们建议此细胞系在基于BmNPV的杆状病毒表达系统中的有用性,也可用于研究体外病毒复制。

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