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分层脑结构中的ErbB4:精神分裂症的神经发育研究方法

ErbB4 in Laminated Brain Structures: A Neurodevelopmental Approach to Schizophrenia.

作者信息

Perez-Garcia Carlos G

机构信息

Molecular Neurobiology Laboratory, The Salk Institute, La Jolla CA, USA.

出版信息

Front Cell Neurosci. 2015 Dec 18;9:472. doi: 10.3389/fncel.2015.00472. eCollection 2015.

Abstract

The susceptibility genes for schizophrenia Neuregulin-1 (NRG1) and ErbB4 have critical functions during brain development and in the adult. Alterations in the ErbB4 signaling pathway cause a variety of neurodevelopmental defects including deficiencies in neuronal migration, synaptic plasticity, and myelination. I have used the ErbB4(-/-) HER4(heart) KO mice to study the neurodevelopmental insults associated to deficiencies in the NRG1-ErbB4 signaling pathway and their potential implication with brain disorders such as schizophrenia, a chronic psychiatric disease affecting 1% of the population worldwide. ErbB4 deletion results in an array of neurodevelopmental deficits that are consistent with a schizophrenic model. First, similar defects appear in multiple brain structures, from the cortex to the cerebellum. Second, these defects affect multiple aspects of brain development, from deficits in neuronal migration to impairments in excitatory/inhibitory systems, including reductions in brain volume, cortical and cerebellar heterotopias, alterations in number and distribution of specific subpopulations of interneurons, deficiencies in the astrocytic and oligodendrocytic lineages, and additional insults in major brain structures. This suggests that alterations in specific neurodevelopmental genes that play similar functions in multiple neuroanatomical structures might account for some of the symptomatology observed in schizophrenic patients, such as defects in cognition. ErbB4 mutation uncovers flaws in brain development that are compatible with a neurodevelopmental model of schizophrenia, and it establishes a comprehensive model to study the basis of the disorder before symptoms are detected in the adult.

摘要

精神分裂症的易感基因神经调节蛋白-1(NRG1)和表皮生长因子受体4(ErbB4)在大脑发育过程及成年期具有关键功能。ErbB4信号通路的改变会导致多种神经发育缺陷,包括神经元迁移、突触可塑性和髓鞘形成方面的不足。我使用ErbB4基因敲除(-/-)的HER4(心脏)基因敲除小鼠来研究与NRG1-ErbB4信号通路缺陷相关的神经发育损伤,以及它们与精神分裂症等脑部疾病的潜在关联。精神分裂症是一种影响全球1%人口的慢性精神疾病。ErbB4基因缺失会导致一系列与精神分裂症模型相符的神经发育缺陷。首先,从皮层到小脑的多个脑结构中都出现了类似的缺陷。其次,这些缺陷影响大脑发育的多个方面,从神经元迁移缺陷到兴奋/抑制系统受损,包括脑容量减少、皮层和小脑异位、中间神经元特定亚群数量和分布改变、星形胶质细胞和少突胶质细胞谱系缺陷,以及主要脑结构的其他损伤。这表明在多个神经解剖结构中发挥相似功能的特定神经发育基因的改变,可能是精神分裂症患者所观察到的一些症状的原因,比如认知缺陷。ErbB4突变揭示了与精神分裂症神经发育模型相符的大脑发育缺陷,并建立了一个综合模型,用于在成年期出现症状之前研究该疾病的发病基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20fd/4683445/61c103072302/fncel-09-00472-g001.jpg

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