Child Study Center, Yale University School of Medicine, 230 South Frontage Rd, New Haven, CT 06520, USA.
Neuropharmacology. 2011 Jun;60(7-8):1355-63. doi: 10.1016/j.neuropharm.2011.02.021. Epub 2011 Mar 1.
Studies in the area of human brain development are critical as research on neurological and psychiatric disorders has advanced, revealing the origins of pathophysiology to be in the earliest developmental stages. Only with a more precise understanding of the genes and environments that influence the brain in these early stages can we address questions about the pathology, diagnosis, prevention and treatment of neuropsychiatric disorders of developmental origin, like autism, schizophrenia, and Tourette syndrome. A new approach for studying early developmental events is the use of induced pluripotent stem cells (iPSCs). These are cells with wide potential, similar to that of embryonic stem cells, derived from mature somatic cells. We review the protocols used to create iPSCs, including the most efficient and reliable reprogramming strategies available to date for generating iPSCs. In addition, we discuss how this new tool can be applied to neuropsychiatric research. The use of iPSCs can advance our understanding of how genes and gene products are dynamically involved in the formation of unique features of the human brain, and how aberrant genetic variation may interfere with its typical formation. The iPSC technology, if properly applied, can also address basic questions about neural differentiation such as how stem cells can be guided into general and specific neurodevelopmental pathways. Current work in neuropsychiatry with iPSCs derived from patients has focused on disorders with specific genetics deficits and those with less-defined origins; it has revealed previously unknown aspects of pathology and potential pharmacological interventions. These exciting advances based on the use of iPSCs hold promise for improving early diagnosis and, possibly, treatment of psychiatric disorders. This article is part of a Special Issue entitled 'Trends in neuropharmacology: in memory of Erminio Costa'.
人类大脑发育领域的研究至关重要,因为神经和精神疾病的研究已经取得了进展,揭示了病理生理学的起源在于最早的发育阶段。只有更精确地了解影响大脑在这些早期阶段的基因和环境,我们才能解决与发育起源的神经精神疾病(如自闭症、精神分裂症和妥瑞氏综合征)的病理学、诊断、预防和治疗相关的问题。研究早期发育事件的一种新方法是使用诱导多能干细胞(iPSC)。这些细胞具有广泛的潜能,类似于胚胎干细胞,由成熟的体细胞衍生而来。我们回顾了创建 iPSC 的方案,包括迄今为止用于生成 iPSC 的最有效和可靠的重编程策略。此外,我们还讨论了如何将这一新工具应用于神经精神疾病研究。iPSC 的使用可以增进我们对基因和基因产物如何动态参与人类大脑独特特征的形成以及异常遗传变异如何干扰其典型形成的理解。如果正确应用 iPSC 技术,还可以解决关于神经分化的基本问题,例如如何指导干细胞进入一般和特定的神经发育途径。目前,基于从患者中提取的 iPSC 进行的神经精神疾病研究集中在具有特定遗传缺陷和起源不明的疾病上;它揭示了病理学和潜在药理学干预的以前未知的方面。这些基于 iPSC 使用的令人兴奋的进展有望改善精神疾病的早期诊断,并且可能改善治疗效果。本文是特刊“神经药理学趋势:纪念 Erminio Costa”的一部分。