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一种用于筛选突触生长突变体的方法揭示了稳定突触强度的机制。

A Screen for Synaptic Growth Mutants Reveals Mechanisms That Stabilize Synaptic Strength.

机构信息

Department of Neurobiology.

Graduate Program in Molecular and Computational Biology, and.

出版信息

J Neurosci. 2019 May 22;39(21):4051-4065. doi: 10.1523/JNEUROSCI.2601-18.2019. Epub 2019 Mar 22.

Abstract

Synapses grow, prune, and remodel throughout development, experience, and disease. This structural plasticity can destabilize information transfer in the nervous system. However, neural activity remains stable throughout life, implying that adaptive countermeasures exist that maintain neurotransmission within proper physiological ranges. Aberrant synaptic structure and function have been associated with a variety of neural diseases, including Fragile X syndrome, autism, and intellectual disability. We have screened 300 mutants in larvae of both sexes for defects in synaptic growth at the neuromuscular junction, identifying 12 mutants with severe reductions or enhancements in synaptic growth. Remarkably, electrophysiological recordings revealed that synaptic strength was unchanged in all but one of these mutants compared with WT. We used a combination of genetic, anatomical, and electrophysiological analyses to illuminate three mechanisms that stabilize synaptic strength despite major disparities in synaptic growth. These include compensatory changes in (1) postsynaptic neurotransmitter receptor abundance, (2) presynaptic morphology, and (3) active zone structure. Together, this characterization identifies new mutants with defects in synaptic growth and the adaptive strategies used by synapses to homeostatically stabilize neurotransmission in response. This study reveals compensatory mechanisms used by synapses to ensure stable functionality during severe alterations in synaptic growth using the neuromuscular junction of as a model system. Through a forward genetic screen, we identify mutants that exhibit dramatic undergrown or overgrown synapses yet express stable levels of synaptic strength, with three specific compensatory mechanisms discovered. Thus, this study reveals novel insights into the adaptive strategies that constrain neurotransmission within narrow physiological ranges while allowing considerable flexibility in overall synapse number. More broadly, these findings provide insights into how stable synaptic function may be maintained in the nervous system during periods of intensive synaptic growth, pruning, and remodeling.

摘要

在发育、经验和疾病过程中,突触会生长、修剪和重塑。这种结构可塑性会使神经系统中的信息传递不稳定。然而,神经活动在整个生命周期中保持稳定,这意味着存在适应性对策,可以将神经传递维持在适当的生理范围内。异常的突触结构和功能与多种神经疾病有关,包括脆性 X 综合征、自闭症和智力障碍。我们对雌雄幼虫中的 300 个突变体进行了筛选,以寻找在神经肌肉接头处突触生长的缺陷,发现了 12 个突变体,其突触生长严重减少或增强。值得注意的是,与 WT 相比,除了一个突变体外,所有这些突变体的突触强度都没有变化。我们使用遗传、解剖和电生理分析的组合,阐明了三种在突触生长存在显著差异的情况下稳定突触强度的机制。这些机制包括(1)突触后神经递质受体丰度、(2)突触前形态和(3)活性区结构的代偿性变化。总之,这种特征鉴定了新的突变体,这些突变体在突触生长缺陷和突触使用的适应性策略中,以响应方式稳定神经传递。本研究使用 作为模型系统,揭示了突触在严重改变突触生长时使用的代偿机制,以确保稳定的功能。通过正向遗传筛选,我们确定了表现出明显生长不足或过度生长的突触,但表达稳定水平的突触强度的突变体,发现了三种特定的代偿机制。因此,本研究揭示了新的见解,即适应性策略如何在狭窄的生理范围内限制神经传递,同时允许整体突触数量具有相当大的灵活性。更广泛地说,这些发现为稳定的突触功能如何在神经生长、修剪和重塑的密集时期在神经系统中得以维持提供了深入的了解。

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