Zhang Xin, Feng Ying, Ding Wei-Feng, Li Xian, Xie Si-Cong
The Key Laboratory of Cultivating and Utilization of Resource Insects of State Forestry Administration, Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, Yunnan, 650224, China.
In Vitro Cell Dev Biol Anim. 2018 Feb;54(2):129-135. doi: 10.1007/s11626-017-0223-5. Epub 2018 Jan 8.
Despite the pest status and medicinal value of the American cockroach Periplaneta americana, few attempts have been made to establish cell lines from this insect owing to the difficulty of culturing Blattarian cells. Here, we describe the establishment of the RIRI-PA1 line from P. americana embryo tissue following primary culture in modified Grace's medium containing 20% fetal bovine serum. RIRI-PA1 was found to primarily consist of attached spindle-shaped and giant cells, which attach themselves to their container. The population-doubling time of 40th-passage cells was approximately 84.8 h. The average chromosome number at the 30th passage was 42, with 40% of cells demonstrating substantial variations, with the highest number of variations of 78 and lowest of 24. The identity of RIRI-PA1 was confirmed by comparing the COI gene of these cells to that of P. americana embryo tissue. Telomerase activity decreased in primary cells after 7 d of culture and 5th-passage cells in comparison to embryo tissues; however, compared to the other cultured cells tested, the telomerase activity significantly increased at the 20th passage. We propose that the stagnation periods and cessation of proliferation observed relate to cellular telomerase activity, but the relationship between insect cell proliferation and telomerase as well as the regulatory mechanism involved remains to be elucidated.
尽管美洲大蠊具有害虫身份和药用价值,但由于培养蜚蠊目细胞存在困难,很少有人尝试从这种昆虫建立细胞系。在此,我们描述了在含有20%胎牛血清的改良Grace培养基中进行原代培养后,从美洲大蠊胚胎组织建立RIRI-PA1细胞系的过程。发现RIRI-PA1主要由附着的纺锤形和巨型细胞组成,这些细胞附着在其容器上。第40代细胞的群体倍增时间约为84.8小时。第30代时的平均染色体数为42条,40%的细胞表现出显著变异,变异数最高为78条,最低为24条。通过将这些细胞的COI基因与美洲大蠊胚胎组织的COI基因进行比较,证实了RIRI-PA1的身份。与胚胎组织相比,原代细胞培养7天后以及第5代细胞的端粒酶活性降低;然而,与测试的其他培养细胞相比,第20代时端粒酶活性显著增加。我们认为观察到的停滞期和增殖停止与细胞端粒酶活性有关,但昆虫细胞增殖与端粒酶之间的关系以及所涉及的调控机制仍有待阐明。