Chen Siyu, Li Zezhi, Yan Quanping, Hua Chenfeng, Shang Pingping, Liu Kejian, Zhao Junwei, Jin Guangxiang, Li Xiang, Xie Fuwei
Key Laboratory of Tobacco Chemistry, Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou, China.
Beijing Life Science Academy, Beijing, China.
Front Bioeng Biotechnol. 2025 Jun 25;13:1570270. doi: 10.3389/fbioe.2025.1570270. eCollection 2025.
Formaldehyde poses a significant threat to human health, yet its toxicity assessment is limited by current detection methods. This study developed a modular biomimetic lung chip which consists of gas concentration gradient generator module and cell culture module, assembled using alignment holes and micropillars. This design enables stepwise experimental procedures, including cell loading, gas concentration gradient exposure, and cell sample collection, through the assembly and disassembly of the modules. Using this chip to investigate the formaldehyde-induced cellular ferroptosis, BEAS-2B cells were exposed to formaldehyde under a concentration gradient. Transcriptomic sequencing revealed the effects of different formaldehyde concentrations on the expression of ferroptosis-related genes in cells, identifying 12 ferroptosis-related genes (FRGS) and an enhancement of oxidative stress. The ferroptosis inhibitor (deferoxamine mesylate) significantly reduced cell death and reactive oxygen species levels, confirming the involvement of ferroptosis in formaldehyde-induced toxicity. Furthermore, deferoxamine mesylate modulated the expression of hub genes of FRGS, including , , , , and , at both transcript and protein levels. These findings provide novel insights into the molecular mechanisms underlying formaldehyde-induced respiratory damage and establish the modular biomimetic lung chip as a powerful platform for studying environmental toxicants.
甲醛对人类健康构成重大威胁,但其毒性评估受到当前检测方法的限制。本研究开发了一种模块化仿生肺芯片,它由气体浓度梯度发生器模块和细胞培养模块组成,通过对准孔和微柱进行组装。这种设计通过模块的组装和拆卸实现了逐步的实验过程,包括细胞加载、气体浓度梯度暴露和细胞样本收集。使用该芯片研究甲醛诱导的细胞铁死亡,将BEAS-2B细胞暴露于浓度梯度的甲醛中。转录组测序揭示了不同甲醛浓度对细胞中铁死亡相关基因表达的影响,鉴定出12个铁死亡相关基因(FRGS)并增强了氧化应激。铁死亡抑制剂(甲磺酸去铁胺)显著降低了细胞死亡和活性氧水平,证实铁死亡参与了甲醛诱导的毒性作用。此外,甲磺酸去铁胺在转录和蛋白质水平上调节了FRGS的枢纽基因的表达,包括 、 、 、 和 。这些发现为甲醛诱导的呼吸道损伤的分子机制提供了新的见解,并将模块化仿生肺芯片确立为研究环境毒物的强大平台。