自闭症谱系障碍小鼠模型概述。
Overview of mouse models of autism spectrum disorders.
作者信息
Bey Alexandra L, Jiang Yong-Hui
机构信息
Department of Neurobiology, Duke University School of Medicine, Durham, North Carolina.
Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina.
出版信息
Curr Protoc Pharmacol. 2014 Sep 2;66:5.66.1-5.66.26. doi: 10.1002/0471141755.ph0566s66.
This overview describes many well characterized mouse models of autism spectrum disorders (ASDs). Mouse models considered here were selected because they are examples of genetically engineered models where human genetic evidence supports a causative relationship between the targeted mutation and the behavioral phenotype. As the ASD diagnosis is based primarily on behavioral evaluations in humans in the domains of social interaction, communication, and restricted interests, the murine phenotypes analogous to human autistic behaviors are highlighted for the different models and behaviors. Although genetically engineered mouse models with good construct and face validity are valuable for identifying and defining underlying pathophysiological mechanisms and for developing potential therapeutic interventions for the human condition, the translational value of various rodent behavioral assays remains a subject of debate. Significant challenges associated with modeling ASDs in rodents because of the clinical and molecular heterogeneity that characterize this disorder are also considered.
本综述描述了许多特征明确的自闭症谱系障碍(ASD)小鼠模型。此处所考虑的小鼠模型是经过挑选的,因为它们是基因工程模型的实例,其中人类遗传证据支持目标突变与行为表型之间的因果关系。由于ASD诊断主要基于人类在社交互动、沟通和兴趣受限领域的行为评估,因此针对不同模型和行为突出了与人类自闭症行为类似的小鼠表型。尽管具有良好构建效度和表面效度的基因工程小鼠模型对于识别和定义潜在病理生理机制以及开发针对人类疾病的潜在治疗干预措施很有价值,但各种啮齿动物行为测定的转化价值仍是一个有争议的话题。文中还考虑了由于该疾病具有临床和分子异质性,在啮齿动物中模拟ASD所面临的重大挑战。