Department of Biochemistry and Molecular Biology, Penn State Hershey Cancer Institute, The Stem Cell and Regenerative Biology Program, Penn State College of Medicine, Hershey, USA.
Sci Rep. 2024 Aug 22;14(1):19522. doi: 10.1038/s41598-024-69912-4.
Individuals with the Autism Susceptibility Candidate 2 (AUTS2) gene disruptions exhibit symptoms such as intellectual disability, microcephaly, growth retardation, and distinct skeletal and facial differences. The role of AUTS2 in neurodevelopment has been investigated using animal and embryonic stem cell models. However, the precise molecular mechanisms of how AUTS2 influences neurodevelopment, particularly in humans, are not thoroughly understood. Our study employed a 3D human cerebral organoid culture system, in combination with genetic, genomic, cellular, and molecular approaches, to investigate how AUTS2 impacts neurodevelopment through cellular signaling pathways. We used CRISPR/Cas9 technology to create AUTS2-deficient human embryonic stem cells and then generated cerebral organoids with these cells. Our transcriptomic analyses revealed that the absence of AUTS2 in cerebral organoids reduces the populations of cells committed to the neuronal lineage, resulting in an overabundance of cells with a transcription profile resembling that of choroid plexus (ChP) cells. Intriguingly, we found that AUTS2 negatively regulates the WNT/β-catenin signaling pathway, evidenced by its overactivation in AUTS2-deficient cerebral organoids and in luciferase reporter cells lacking AUTS2. Importantly, treating the AUTS2-deficient cerebral organoids with a WNT inhibitor reversed the overexpression of ChP genes and increased the downregulated neuronal gene expression. This study offers new insights into the role of AUTS2 in neurodevelopment and suggests potential targeted therapies for neurodevelopmental disorders.
个体携带自闭症易感性候选基因 2 (AUTS2) 突变会表现出智力障碍、小头畸形、生长迟缓以及明显的骨骼和面部差异等症状。已经使用动物和胚胎干细胞模型研究了 AUTS2 在神经发育中的作用。然而,AUTS2 如何影响神经发育的精确分子机制,特别是在人类中,还没有被完全理解。我们的研究使用了 3D 人类大脑类器官培养系统,结合遗传、基因组、细胞和分子方法,研究了 AUTS2 通过细胞信号通路如何影响神经发育。我们使用 CRISPR/Cas9 技术创建了 AUTS2 缺失的人类胚胎干细胞,然后用这些细胞生成大脑类器官。我们的转录组分析表明,大脑类器官中 AUTS2 的缺失减少了向神经元谱系分化的细胞群体,导致具有类似于脉络丛 (ChP) 细胞转录特征的细胞过多。有趣的是,我们发现 AUTS2 负调控 WNT/β-catenin 信号通路,这一点可以从 AUTS2 缺失的大脑类器官和缺乏 AUTS2 的荧光素酶报告细胞中 WNT/β-catenin 信号的过度激活得到证明。重要的是,用 WNT 抑制剂处理 AUTS2 缺失的大脑类器官可以逆转 ChP 基因的过表达,并增加下调的神经元基因表达。这项研究为 AUTS2 在神经发育中的作用提供了新的见解,并为神经发育障碍的潜在靶向治疗提供了依据。