Scott Michael M, Deneris Evan S
Department of Neuroscience, School of Medicine, Case Western Reserve University, Rm E732, 2109 Adelbert Road, Cleveland, OH 44106-4975, USA.
Int J Dev Neurosci. 2005 Apr-May;23(2-3):277-85. doi: 10.1016/j.ijdevneu.2004.05.012.
Dysfunction of brain serotonin system development is hypothesized to contribute to autistic behaviors. The testing of this hypothesis will likely depend on a better understanding of the genes and mechanisms involved in serotonin neuron cell fate specification. In this review we summarize the main features of vertebrate serotonin neuroanatomical development and recent studies that have revealed critical steps in the molecular genetic program that controls serotonin neuron phenotype. We then discuss the potential relevance of these findings to advances in autism research and to new molecular genetic tools under development that will impact future testing of the hypothesis.
大脑血清素系统发育功能障碍被认为与自闭症行为有关。对这一假设的验证可能依赖于对血清素神经元细胞命运特化所涉及的基因和机制有更深入的了解。在这篇综述中,我们总结了脊椎动物血清素神经解剖学发育的主要特征以及最近的研究,这些研究揭示了控制血清素神经元表型的分子遗传程序中的关键步骤。然后,我们讨论了这些发现与自闭症研究进展以及正在开发的新分子遗传工具的潜在相关性,这些工具将影响该假设未来的验证。