Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN, 47907, USA.
Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47907, USA.
Environ Int. 2024 Aug;190:108914. doi: 10.1016/j.envint.2024.108914. Epub 2024 Jul 26.
PFOA is a legacy Per- and Polyfluorinated Substances (PFAS), a group of chemicals widely used in various industrial applications and consumer products. Although there has been a voluntary phase out of PFOA since 2005, it is still widely detected in various water supplies. A growing body of evidence suggests an association between PFOA exposure, particularly during developmental stages, with increased risks of neurodegenerative diseases (NDs). The neurotoxic mechanism of developmental PFOA exposure, however, remains poorly understood. Utilizing human induced-pluripotent stem cell (hiPSC)-derived cortical neurons, we investigated the effect of PFOA exposure prior to differentiation and assessed changes in neuronal characteristics, transcriptome, and neurodegeneration markers mimicking a Developmental Origin of Health and Disease (DoHAD) paradigm. Exposure to PFOA before neuron differentiation resulted in persistent alterations in nuclear morphology, neuronal network, and calcium activity. RNA sequencing analysis further revealed transcriptomic changes aligning with Alzheimer's Disease (AD) after PFOA exposure. These observations were further corroborated by alterations in tau phosphorylation markers, the presence of fibrillar tau, an increase in liquid droplets, and a decrease in RNA translational efficiency characterized using a battery of biochemical assays. Taken together, our results revealed persistent deficits of key neuronal characteristics induced by pre-differentiation PFOA exposure, suggesting impairments in several AD-related pathways that can together contribute to the elevation of AD risk after pre-differentiation PFOA exposure.
全氟辛酸(PFOA)是一种遗留的全氟和多氟化合物(PFAS),是一组广泛应用于各种工业应用和消费产品中的化学物质。尽管自 2005 年以来已经自愿淘汰了 PFOA,但它仍然在各种水源中广泛检测到。越来越多的证据表明,PFOA 暴露,特别是在发育阶段,与神经退行性疾病(NDs)的风险增加之间存在关联。然而,发育性 PFOA 暴露的神经毒性机制仍知之甚少。利用人诱导多能干细胞(hiPSC)衍生的皮质神经元,我们研究了分化前 PFOA 暴露的影响,并评估了模拟健康和疾病的发育起源(DoHAD)范式的神经元特征、转录组和神经退行性变标志物的变化。在神经元分化之前暴露于 PFOA 会导致核形态、神经元网络和钙活性的持续改变。RNA 测序分析进一步揭示了 PFOA 暴露后与阿尔茨海默病(AD)一致的转录组变化。这些观察结果进一步通过tau 磷酸化标志物的改变、纤维状 tau 的存在、液滴的增加以及使用一系列生化测定法测定的 RNA 翻译效率的降低得到证实。总之,我们的结果揭示了分化前 PFOA 暴露诱导的关键神经元特征的持续缺陷,这表明 AD 相关途径的几个受损可能共同导致分化前 PFOA 暴露后 AD 风险的升高。