The Hussman Institute for Autism, 801 W. Baltimore St., Suite 301, Baltimore, Maryland, 21201.
Autism Res. 2016 May;9(5):513-35. doi: 10.1002/aur.1570. Epub 2015 Oct 1.
Autism Spectrum Disorder (ASD) is a behaviorally defined neurodevelopmental condition. Symptoms of ASD cover the spectrum from mild qualitative differences in social interaction to severe communication and social and behavioral challenges that require lifelong support. Attempts at understanding the pathophysiology of ASD have been hampered by a multifactorial etiology that stretches the limits of current behavioral and cell based models. Recent progress has implicated numerous autism-risk genes but efforts to gain a better understanding of the underlying biological mechanisms have seen slow progress. This is in part due to lack of appropriate models for complete molecular and pharmacological studies. The advent of induced pluripotent stem cells (iPSC) has reinvigorated efforts to establish more complete model systems that more reliably identify molecular pathways and predict effective drug targets and candidates in ASD. iPSCs are particularly appealing because they can be derived from human patients and controls for research purposes and provide a technology for the development of a personalized treatment regimen for ASD patients. The pluripotency of iPSCs allow them to be reprogrammed into a number of CNS cell types and phenotypically screened across many patients. This quality is already being exploited in protocols to generate 2-dimensional (2-D) and three-dimensional (3-D) models of neurons and developing brain structures. iPSC models make powerful platforms that can be interrogated using electrophysiology, gene expression studies, and other cell-based quantitative assays. iPSC technology has limitations but when combined with other model systems has great potential for helping define the underlying pathophysiology of ASD. Autism Res 2016, 9: 513-535. © 2015 International Society for Autism Research, Wiley Periodicals, Inc.
自闭症谱系障碍 (ASD) 是一种行为定义的神经发育障碍。ASD 的症状涵盖了从社交互动方面轻微的定性差异到严重的沟通和社交及行为挑战的范围,这些挑战需要终生支持。尝试理解 ASD 的病理生理学受到多因素病因的阻碍,这种病因超出了当前基于行为和细胞的模型的限制。最近的进展表明了许多自闭症风险基因的存在,但为了更好地理解潜在的生物学机制,进展缓慢。部分原因是缺乏用于完整分子和药理学研究的适当模型。诱导多能干细胞 (iPSC) 的出现重新激发了建立更完整模型系统的努力,这些模型系统更可靠地确定分子途径,并预测 ASD 中的有效药物靶点和候选药物。iPSC 特别吸引人,因为它们可以从人类患者和对照中获得,用于研究目的,并为 ASD 患者开发个性化治疗方案提供了技术。iPSC 的多能性允许它们被重新编程为多种 CNS 细胞类型,并在许多患者中进行表型筛选。这种特性已经在生成神经元和发育中脑结构的 2 维 (2-D) 和 3 维 (3-D) 模型的方案中得到了利用。iPSC 模型是强大的平台,可以通过电生理学、基因表达研究和其他基于细胞的定量分析进行研究。iPSC 技术存在局限性,但与其他模型系统结合具有很大的潜力,可以帮助确定 ASD 的潜在病理生理学。自闭症研究 2016, 9: 513-535。© 2015 自闭症国际研究协会,威利期刊,公司。