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氨基酸降解途径抑制副产物诱导 CHO 细胞凋亡。

Amino acid degradation pathway inhibitory by-products trigger apoptosis in CHO cells.

机构信息

ARC Training Centre for Biopharmaceutical Innovation (CBI), Australian Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, St Lucia, Queensland, Australia.

Queensland Metabolomics and Proteomics (Q-MAP), The University of Queensland, St Lucia, Queensland, Australia.

出版信息

Biotechnol J. 2024 Jan;19(2):e2300338. doi: 10.1002/biot.202300338.

Abstract

Chinese hamster ovary (CHO) cells are widely used to produce complex biopharmaceuticals. Improving their productivity is necessary to fulfill the growing demand for such products. One way to enhance productivity is by cultivating cells at high densities, but inhibitory by-products, such as metabolite derivatives from amino acid degradation, can hinder achieving high cell densities. This research examines the impact of these inhibitory by-products on high-density cultures. We cultured X1 and X2 CHO cell lines in a small-scale semi-perfusion system and introduced a mix of inhibitory by-products on day 10. The X1 and X2 cell lines were chosen for their varied responses to the by-products; X2 was susceptible, while X1 survived. Proteomics revealed that the X2 cell line presented changes in the proteins linked to apoptosis regulation, cell building block synthesis, cell growth, DNA repair, and energy metabolism. We later used the AB cell line, an apoptosis-resistant cell line, to validate the results. AB behaved similar to X1 under stress. We confirmed the activation of apoptosis in X2 using a caspase assay. This research provides insights into the mechanisms of cell death triggered by inhibitory by-products and can guide the optimization of CHO cell culture for biopharmaceutical manufacturing.

摘要

中国仓鼠卵巢(CHO)细胞广泛用于生产复杂的生物制药。为了满足对这类产品不断增长的需求,提高它们的生产力是必要的。一种提高生产力的方法是在高密度下培养细胞,但抑制性的副产物,如氨基酸降解的代谢物衍生物,可能会阻碍达到高细胞密度。这项研究考察了这些抑制性副产物对高密度培养的影响。我们在小规模半灌注系统中培养了 X1 和 X2 CHO 细胞系,并在第 10 天引入了抑制性副产物的混合物。选择 X1 和 X2 细胞系是因为它们对副产物的反应不同;X2 敏感,而 X1 存活。蛋白质组学揭示,X2 细胞系的蛋白表达发生了变化,这些蛋白与细胞凋亡调控、细胞构建块合成、细胞生长、DNA 修复和能量代谢有关。后来,我们使用了 AB 细胞系,一种抗凋亡细胞系,来验证结果。AB 在压力下的表现与 X1 相似。我们使用半胱氨酸天冬氨酸蛋白酶测定法证实了 X2 中细胞凋亡的激活。这项研究深入了解了抑制性副产物引发细胞死亡的机制,并为优化用于生物制药生产的 CHO 细胞培养提供了指导。

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