Ziats Mark N, Edmonson Catherine, Rennert Owen M
National Institute of Child Health and Human Development, NIH Bethesda, MD, USA ; Medical Scientist Training Program, Baylor College of Medicine Houston, TX, USA.
National Institute of Child Health and Human Development, NIH Bethesda, MD, USA ; College of Medicine, University of Florida Gainesville, FL, USA.
Front Neuroanat. 2015 Aug 25;9:115. doi: 10.3389/fnana.2015.00115. eCollection 2015.
The etiology of autism spectrum disorders (ASDs) is complex and largely unclear. Among various lines of inquiry, many have suggested convergence onto disruptions in both neural circuitry and immune regulation/glial cell function pathways. However, the interpretation of the relationship between these two putative mechanisms has largely focused on the role of exogenous factors and insults, such as maternal infection, in activating immune pathways that in turn result in neural network abnormalities. Yet, given recent insights into our understanding of human neurodevelopment, and in particular the critical role of glia and the immune system in normal brain development, it is important to consider these putative pathological processes in their appropriate normal neurodevelopmental context. In this review, we explore the hypothesis that the autistic brain cellular phenotype likely represents intrinsic abnormalities of glial/immune processes constitutively operant in normal brain development that result in the observed neural network dysfunction. We review recent studies demonstrating the intercalated role of neural circuit development, the immune system, and glial cells in the normal developing brain, and integrate them with studies demonstrating pathological alterations in these processes in autism. By discussing known abnormalities in the autistic brain in the context of normal brain development, we explore the hypothesis that the glial/immune component of ASD may instead be related to intrinsic exaggerated/abnormal constitutive neurodevelopmental processes such as network pruning. Moreover, this hypothesis may be relevant to other neurodevelopmental disorders that share genetic, pathologic, and clinical features with autism.
自闭症谱系障碍(ASD)的病因复杂,在很大程度上尚不清楚。在各种研究方向中,许多研究表明,神经回路以及免疫调节/神经胶质细胞功能通路的破坏存在共同之处。然而,对这两种假定机制之间关系的解释主要集中在外源性因素和损伤的作用上,例如母体感染,这些因素激活免疫通路,进而导致神经网络异常。然而,鉴于我们对人类神经发育的最新认识,尤其是神经胶质细胞和免疫系统在正常大脑发育中的关键作用,在适当的正常神经发育背景下考虑这些假定的病理过程非常重要。在这篇综述中,我们探讨了这样一种假说,即自闭症大脑的细胞表型可能代表了正常大脑发育过程中持续存在的神经胶质/免疫过程的内在异常,这些异常导致了观察到的神经网络功能障碍。我们回顾了最近的研究,这些研究证明了神经回路发育、免疫系统和神经胶质细胞在正常发育大脑中的穿插作用,并将它们与证明自闭症中这些过程存在病理改变的研究相结合。通过在正常大脑发育的背景下讨论自闭症大脑中已知的异常情况,我们探讨了这样一种假说,即ASD的神经胶质/免疫成分可能反而与内在的过度/异常的组成性神经发育过程有关,例如网络修剪。此外,这一假说可能与其他与自闭症具有遗传、病理和临床特征的神经发育障碍有关。