Department of Pediatrics & Human Development, Michigan State University, Grand Rapids, Michigan, USA.
Center for Research in Autism, Intellectual, and other Neurodevelopmental Disabilities, Michigan State University, East Lansing, Michigan, USA.
Dev Neurosci. 2020;42(5-6):195-207. doi: 10.1159/000513536. Epub 2021 Mar 3.
Autism spectrum disorder (ASD) manifests early in childhood. While genetic variants increase risk for ASD, a growing body of literature has established that in utero chemical exposures also contribute to ASD risk. These chemicals include air-based pollutants like diesel particulate matter (DPM). A combination of single-cell and direct transcriptomics of DPM-exposed human-induced pluripotent stem cell-derived cerebral organoids revealed toxicogenomic effects of DPM exposure during fetal brain development. Direct transcriptomics, sequencing RNA bases via Nanopore, revealed that cerebral organoids contain extensive RNA modifications, with DPM-altering cytosine methylation in oxidative mitochondrial transcripts expressed in outer radial glia cells. Single-cell transcriptomics further confirmed an oxidative phosphorylation change in cell groups such as outer radial glia upon DPM exposure. This approach highlights how DPM exposure perturbs normal mitochondrial function and cellular respiration during early brain development, which may contribute to developmental disorders like ASD by altering neurodevelopment.
自闭症谱系障碍(ASD)在儿童早期表现出来。虽然遗传变异会增加患 ASD 的风险,但越来越多的文献已经证实,子宫内的化学暴露也会导致 ASD 风险。这些化学物质包括空气中的污染物,如柴油颗粒物(DPM)。对暴露于 DPM 的人类诱导多能干细胞衍生的大脑类器官进行单细胞和直接转录组学的组合研究表明,DPM 暴露在胎儿大脑发育过程中会产生毒理基因组效应。通过纳米孔进行 RNA 碱基测序的直接转录组学揭示,大脑类器官中含有广泛的 RNA 修饰,DPM 改变了在外放射状胶质细胞中表达的氧化线粒体转录物中的胞嘧啶甲基化。单细胞转录组学进一步证实,DPM 暴露后,外放射状胶质等细胞群中的氧化磷酸化发生变化。这种方法强调了 DPM 暴露如何在早期大脑发育过程中扰乱正常的线粒体功能和细胞呼吸,这可能通过改变神经发育而导致 ASD 等发育障碍。