Palmisano Salvator, Breidenbach Joshua D, Blackwell Brett R, Harvey Tara, Luchini Kes A, Thornhill M Grace, LeBrun Erick S, Mach Phillip, Glaros Trevor, Rivera Emilio S
Biochemistry and Biotechnology Group (B-TEK), Bioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.
LMI, Colorado Springs, CO 80919, USA.
Cells. 2025 May 29;14(11):803. doi: 10.3390/cells14110803.
Primary human hepatocytes (PHHs) are widely used as in vitro models for liver function and drug metabolism studies, yet their metabolic stability post-thawing remains an open question. To better characterize early metabolic changes, we conducted a time-course experiment using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to analyze metabolic shifts in PHHs cultured in suspension. Unexposed and exposed (acetaminophen-treated) samples were evaluated, and TITAN analysis was applied to determine the time point of maximal metabolic change at both individual metabolite and global metabolic profile levels. Our results indicate that the majority of metabolic shifts occur within the first five hours post-thawing. In the early culture time points, substantial metabolic overlap was observed between unexposed and exposed cells, suggesting a conserved biological response likely related to cellular recovery. However, at later time points, metabolite profiles diverged, with acetaminophen treatment-specific metabolic changes emerging, potentially reflecting differences in homeostatic restoration versus hepatotoxic responses. Our study highlights the importance of considering early post-thawing metabolic dynamics in experimental design and offers insights for optimizing hepatocyte culture protocols to better replicate in vivo physiological conditions.
原代人肝细胞(PHHs)被广泛用作肝功能和药物代谢研究的体外模型,但其解冻后的代谢稳定性仍是一个悬而未决的问题。为了更好地表征早期代谢变化,我们进行了一项时间进程实验,使用液相色谱-串联质谱(LC-MS/MS)分析悬浮培养的PHHs中的代谢变化。对未暴露和暴露(对乙酰氨基酚处理)的样本进行了评估,并应用TITAN分析来确定在个体代谢物和整体代谢谱水平上最大代谢变化的时间点。我们的结果表明,大多数代谢变化发生在解冻后的前五个小时内。在早期培养时间点,未暴露和暴露细胞之间观察到大量代谢重叠,这表明可能存在与细胞恢复相关的保守生物学反应。然而,在后期时间点,代谢物谱出现分歧,出现了对乙酰氨基酚处理特异性的代谢变化,这可能反映了稳态恢复与肝毒性反应的差异。我们的研究强调了在实验设计中考虑解冻后早期代谢动态的重要性,并为优化肝细胞培养方案以更好地复制体内生理条件提供了见解。