Hwang Sun Ok, Lee Gyun Min
Department of Biological Sciences, KAIST, 335 Gwahangno, Yuseong-gu, Daejeon, 305-701, Republic of Korea.
J Biotechnol. 2009 Jan 1;139(1):89-94. doi: 10.1016/j.jbiotec.2008.09.008. Epub 2008 Oct 14.
Upon nutrient deprivation, Chinese hamster ovary (CHO) cells are subjected to two types of programmed cell death, apoptosis and autophagy. CHO cell engineering, as a means to improve foreign protein production, has focused mainly on anti-apoptosis. In this study, to determine the effect of Akt, which is known to regulate both apoptosis and autophagy, on cell survival and foreign protein production, constitutively active Akt was overexpressed in antibody-producing cells. Compared with the control cells, Akt overexpressing cells showed delayed onset of apoptosis and autophagy during batch culture. The inhibition of apoptosis was demonstrated by reduced amount of cleaved poly(ADP-ribose) polymerase and caspase 3 proteins and less fragmentation of chromosomal DNA. Moreover, under nutrient-limiting conditions, decreased level of autophagosome accumulation was observed in Akt overexpressing cells by the less accumulation of the 16kDa form of LC3-II and autophagic vacuoles. Taken together, the overexpression of constitutively active Akt in CHO cells could delay the onset of both types of programmed cell death during batch culture.
在营养缺乏的情况下,中国仓鼠卵巢(CHO)细胞会经历两种程序性细胞死亡,即凋亡和自噬。CHO细胞工程作为提高外源蛋白产量的一种手段,主要集中在抗凋亡方面。在本研究中,为了确定已知可调节凋亡和自噬的Akt对细胞存活和外源蛋白生产的影响,在产生抗体的细胞中过表达组成型活性Akt。与对照细胞相比,过表达Akt的细胞在分批培养过程中凋亡和自噬的起始延迟。通过裂解的聚(ADP - 核糖)聚合酶和半胱天冬酶3蛋白量的减少以及染色体DNA片段化减少证明了凋亡的抑制。此外,在营养限制条件下,通过LC3 - II的16kDa形式和自噬泡的积累减少,在过表达Akt的细胞中观察到自噬体积累水平降低。综上所述,在CHO细胞中组成型活性Akt的过表达可在分批培养期间延迟两种程序性细胞死亡的起始。