Acab Allan, Muotri Alysson Renato
School of Medicine, Department of Pediatrics/Rady Children's Hospital San Diego, Department of Cellular and Molecular Medicine, Stem Cell Program, University of California San Diego, MC 0695, La Jolla, CA, 92093, USA.
Neurotherapeutics. 2015 Jul;12(3):534-45. doi: 10.1007/s13311-015-0354-x.
Autism spectrum disorders (ASDs) are a heterogeneous group of neurodevelopmental disorders sharing a core set of symptoms, including impaired social interaction, language deficits, and repetitive behaviors. While ASDs are highly heritable and demonstrate a clear genetic component, the cellular and molecular mechanisms driving ASD etiology remain undefined. The unavailability of live patient-specific neurons has contributed to the difficulty in studying ASD pathophysiology. The recent advent of induced pluripotent stem cells (iPSCs) has provided the ability to generate patient-specific human neurons from somatic cells. The iPSC field has quickly grown, as researchers have demonstrated the utility of this technology to model several diseases, especially neurologic disorders. Here, we review the current literature around using iPSCs to model ASDs, and discuss the notable findings, and the promise and limitations of this technology. The recent report of a nonsyndromic ASD iPSC model and several previous ASD models demonstrating similar results points to the ability of iPSC to reveal potential novel biomarkers and therapeutics.
自闭症谱系障碍(ASD)是一组异质性神经发育障碍,具有一系列核心症状,包括社交互动受损、语言缺陷和重复行为。虽然ASD具有高度遗传性并显示出明确的遗传成分,但驱动ASD病因的细胞和分子机制仍不明确。缺乏活体患者特异性神经元导致了研究ASD病理生理学的困难。诱导多能干细胞(iPSC)的最新出现提供了从体细胞生成患者特异性人类神经元的能力。iPSC领域迅速发展,因为研究人员已经证明了这项技术在模拟多种疾病,尤其是神经系统疾病方面的实用性。在这里,我们综述了目前关于使用iPSC模拟ASD的文献,并讨论了显著发现以及该技术的前景和局限性。最近一份关于非综合征性ASD iPSC模型的报告以及之前几个显示类似结果的ASD模型表明,iPSC有能力揭示潜在的新型生物标志物和治疗方法。