Kim Dongil, Yoon Chansik, Lee Gyun Min
Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.
Biotechnol Bioeng. 2022 Mar;119(3):820-831. doi: 10.1002/bit.28013. Epub 2022 Jan 5.
Small molecule epigenetic modulators that modify epigenetic states in cells are useful tools for regulating gene expression by inducing chromatin remodeling. To identify small molecule epigenetic modulators that enhance recombinant protein expression in Chinese hamster ovary (CHO) cells, we examined eight histone deacetylase inhibitors (iHDACs) and six DNA methyltransferase inhibitors as chemical additives in recombinant CHO (rCHO) cell cultures. Among these, a benzamide-based iHDAC, CI994, was the most effective in increasing monoclonal antibody (mAb) production. Despite suppressing cell growth, the addition of CI994 to mAb-expressing GSR cell cultures at 10 μM resulted in a 2.3-fold increase in maximum mAb concentration due to a 3.0-fold increase in specific mAb productivity (q ). CI994 increased mAb messenger RNA levels and histone H3 acetylation in GSR cells, and chromatin immunoprecipitation-quantitative polymerase chain reaction analysis revealed that CI994 significantly increased the histone H3 acetylation level at the cytomegalovirus promoter driving mAb gene expression, indicating that chromatin remodeling in the promoter region results in enhanced mAb gene transcription and q . Similar beneficial effects of CI994 on mAb production were observed in mAb-expressing CS13-1.00 cells. Collectively, our findings indicate that CI994 increases mAb production in rCHO cell cultures by chromatin remodeling resulting from acetylation of histones in the mAb gene promoter.
能够改变细胞表观遗传状态的小分子表观遗传调节剂是通过诱导染色质重塑来调控基因表达的有用工具。为了鉴定能够增强中国仓鼠卵巢(CHO)细胞中重组蛋白表达的小分子表观遗传调节剂,我们检测了八种组蛋白去乙酰化酶抑制剂(iHDACs)和六种DNA甲基转移酶抑制剂作为重组CHO(rCHO)细胞培养中的化学添加剂。其中,一种基于苯甲酰胺的iHDAC,CI994,在增加单克隆抗体(mAb)产量方面最为有效。尽管CI994抑制细胞生长,但在表达mAb的GSR细胞培养物中添加10 μM的CI994,由于特异性mAb生产率(q)提高了3.0倍,导致最大mAb浓度增加了2.3倍。CI994增加了GSR细胞中mAb信使RNA水平和组蛋白H3乙酰化,染色质免疫沉淀-定量聚合酶链反应分析表明,CI994显著增加了驱动mAb基因表达的巨细胞病毒启动子处的组蛋白H3乙酰化水平,表明启动子区域的染色质重塑导致mAb基因转录和q增强。在表达mAb的CS13-1.00细胞中也观察到了CI994对mAb产生的类似有益作用。总的来说,我们的研究结果表明,CI994通过mAb基因启动子中组蛋白乙酰化导致的染色质重塑来增加rCHO细胞培养物中的mAb产量。