Pol Pérez-Rubio , Elianet Lorenzo Romero , Laura Cervera , Francesc Gòdia , Lars Keld Nielsen , Jesús Lavado-García
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引用次数: 0
Abstract
Understanding the molecular mechanisms governing transfection efficiency and particle secretion in high cell density cultures is critical to overcome the cell density effect upon transient gene expression. The effect of different conditioned media in HEK293 transcriptome at low and high cell density is explored. A systematic pair-wise comparative study was performed to shed light on the effect on previous phenotypical characteristics of different media conditions: fresh, exhausted and media depleted from extracellular vesicles (EVs) as well as associated proteins and RNAs. The obtained results suggest that restorative effects observed in transfection efficiency when employing EV-depleted media may arise predominantly from physicochemical alterations rather than cellular processes. A significant downregulation of genes associated with nucleocytoplasmic transport for the conditions involving the use of exhausted or EV-depleted media was observed. Moreover, upregulation of histone-related genes in EV-depleted media suggest a role for histone signaling in response to cellular stress or growth limitations, thereby highlighting the potential of manipulating histone levels as a promising strategy to enhance transient transfection. It was also corroborated that the accumulation of extracellular matrix proteins upon cell growth may inhibit transfection by an already-known competitive effect between cell membrane-bound and free proteoglycans. Proteomic characterization of EV-depleted media further unveiled enrichment of pathways associated with infection response and double-strand DNA breaks, suggesting that HEK293 cells undergo an induced infection-like state that disrupts cellular processes. Importantly, the study reveals that EV-depleted media stimulates virion release pathways underscoring the complex interplay between extracellular vesicles and viral budding.
要克服细胞密度对瞬时基因表达的影响,了解高细胞密度培养中转染效率和微粒分泌的分子机制至关重要。本研究探讨了不同条件培养基在低细胞密度和高细胞密度下对 HEK293 转录组的影响。研究人员进行了一项系统的配对比较研究,以揭示不同培养基条件对先前表型特征的影响:新鲜培养基、耗竭培养基和去除了细胞外囊泡 (EV) 以及相关蛋白质和 RNA 的培养基。研究结果表明,在使用去除了细胞外囊泡的培养基时,转染效率的恢复效果可能主要来自理化改变,而不是细胞过程。在使用耗尽或 EV 贫化培养基的条件下,观察到与核胞质转运相关的基因明显下调。此外,组蛋白相关基因在 EV 贫化培养基中的上调表明,组蛋白信号转导在应对细胞压力或生长限制方面发挥了作用,从而凸显了操纵组蛋白水平作为一种增强瞬时转染策略的潜力。研究还证实,细胞生长时细胞外基质蛋白的积累可能会通过细胞膜结合蛋白和游离蛋白聚糖之间已知的竞争效应抑制转染。EV贫化培养基的蛋白质组学特征进一步揭示了与感染反应和双链DNA断裂相关的通路的富集,表明HEK293细胞经历了一种类似感染的诱导状态,从而破坏了细胞过程。重要的是,该研究揭示了 EV 贫化培养基刺激病毒释放途径,强调了细胞外囊泡与病毒出芽之间复杂的相互作用。
期刊介绍:
Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.