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将基因转移到由 mGluR5 含量突触连接的新皮层前突触和后突触神经元中。

Separate Gene Transfers into Pre- and Postsynaptic Neocortical Neurons Connected by mGluR5-Containing Synapses.

机构信息

Department of Ophthalmology, Louisiana State University Health Sciences Center, New Orleans, USA.

Department of Pharmacology, Louisiana State University Health Sciences Center, New Orleans, USA.

出版信息

J Mol Neurosci. 2019 Aug;68(4):549-564. doi: 10.1007/s12031-019-01317-9. Epub 2019 Apr 10.

Abstract

mGluR5-containing synapses have essential roles in synaptic plasticity, circuit physiology, and learning, and dysfunction at these synapses is implicated in specific neurological disorders. As mGluR5-containing synapses are embedded in large and complex distributed circuits containing many neuron and synapse types, it is challenging to elucidate the roles of these synapses and to develop treatments for the associated disorders. Thus, it would be advantageous to deliver different genes into pre- and postsynaptic neurons connected by a mGluR5-containing synapse. Here, we develop this capability: The first gene transfer, into the presynaptic neurons, uses standard techniques to deliver a vector that expresses a synthetic peptide neurotransmitter. This peptide neurotransmitter has three domains: a dense core vesicle sorting domain, a mGluR5-binding domain composed of a single-chain variable fragment anti-mGluR5, and the His tag. Upon release, this peptide neurotransmitter binds to mGluR5, predominately located on the postsynaptic neurons. Selective gene transfer into these neurons uses antibody-mediated, targeted gene transfer and anti-His tag antibodies, as the synthetic peptide neurotransmitter contains the His tag. For the model system, we studied the connection between neurons in two neocortical areas: postrhinal and perirhinal cortices. Targeted gene transfer was over 80% specific for mGluR5-containing synapses, but untargeted gene transfer was only ~ 15% specific for these synapses. This technology may enable studies on the roles of mGluR5-containing neurons and synapses in circuit physiology and learning and support gene therapy treatments for specific disorders that involve dysfunction at these synapses.

摘要

mGluR5 包含的突触在突触可塑性、电路生理学和学习中起着重要作用,这些突触的功能障碍与特定的神经障碍有关。由于 mGluR5 包含的突触嵌入在包含许多神经元和突触类型的大型和复杂的分布式电路中,因此阐明这些突触的作用并开发相关疾病的治疗方法具有挑战性。因此,将不同的基因递送到由 mGluR5 包含的突触连接的前突触和后突触神经元中是有利的。在这里,我们开发了这种能力:第一个基因转移到前突触神经元中,使用标准技术来传递表达合成肽神经递质的载体。这种肽神经递质具有三个结构域:致密核心囊泡分拣结构域、由单链可变片段抗 mGluR5 组成的 mGluR5 结合结构域,以及 His 标签。释放后,这种肽神经递质与主要位于后突触神经元上的 mGluR5 结合。使用抗体介导的靶向基因转移和抗 His 标签抗体对这些神经元进行选择性基因转移,因为合成肽神经递质包含 His 标签。对于模型系统,我们研究了两个新皮质区域(后边缘皮质和旁边缘皮质)之间神经元的连接。靶向基因转移对 mGluR5 包含的突触的特异性超过 80%,但非靶向基因转移对这些突触的特异性仅约为 15%。这项技术可能使我们能够研究 mGluR5 包含的神经元和突触在电路生理学和学习中的作用,并支持针对涉及这些突触功能障碍的特定疾病的基因治疗。

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