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嗅球注射α-突触核蛋白纤维后聚集体的扩散与早期神经元丢失有关,并长期减少。

Spread of aggregates after olfactory bulb injection of α-synuclein fibrils is associated with early neuronal loss and is reduced long term.

机构信息

Center for Neurodegenerative Science, Van Andel Research Institute, 333 Bostwick Avenue N.E., Grand Rapids, MI, 49503, USA.

Bioinformatics and Biostatistics Core, Van Andel Research Institute, 333 Bostwick Avenue N.E., Grand Rapids, MI, 49503, USA.

出版信息

Acta Neuropathol. 2018 Jan;135(1):65-83. doi: 10.1007/s00401-017-1792-9. Epub 2017 Dec 5.

Abstract

Parkinson's disease is characterized by degeneration of substantia nigra dopamine neurons and by intraneuronal aggregates, primarily composed of misfolded α-synuclein. The α-synuclein aggregates in Parkinson's patients are suggested to first appear in the olfactory bulb and enteric nerves and then propagate, following a stereotypic pattern, via neural pathways to numerous regions across the brain. We recently demonstrated that after injection of either mouse or human α-synuclein fibrils into the olfactory bulb of wild-type mice, α-synuclein fibrils recruited endogenous α-synuclein into pathological aggregates that spread transneuronally to over 40 other brain regions and subregions, over 12 months. We previously reported the progressive spreading of α-synuclein aggregates, between 1 and 12 months following α-synuclein fibril injections, and now report how far the pathology has spread 18- and 23-month post-injection in this model. Our data show that between 12 and 18 months, there is a further increase in the number of brain regions exhibiting pathology after human, and to a lesser extent mouse, α-synuclein fibril injections. At both 18 and 23 months after injection of mouse and human α-synuclein fibrils, we observed a reduction in the density of α-synuclein aggregates in some brain regions compared to others at 12 months. At 23 months, no additional brain regions exhibited α-synuclein aggregates compared to earlier time points. In addition, we also demonstrate that the induced α-synucleinopathy triggered a significant early neuron loss in the anterior olfactory nucleus. By contrast, there was no loss of mitral neurons in the olfactory bulb, even at 18 month post-injection. We speculate that the lack of continued progression of α-synuclein pathology is due to compromise of the neural circuitry, consequential to neuron loss and possibly to the activation of proteolytic mechanisms in resilient neurons of wild-type mice that counterbalances the spread and seeding by degrading pathogenic α-synuclein.

摘要

帕金森病的特征是黑质多巴胺神经元退化和细胞内聚集体,主要由错误折叠的α-突触核蛋白组成。帕金森病患者的α-突触核蛋白聚集体被认为首先出现在嗅球和肠神经中,然后沿着刻板的模式通过神经通路传播到大脑的许多区域。我们最近证明,无论是将小鼠还是人类的α-突触核蛋白原纤维注射到野生型小鼠的嗅球中,α-突触核蛋白原纤维都会招募内源性α-突触核蛋白进入病理聚集体,这些聚集体通过神经元间传播到大脑的 40 多个其他区域和亚区,超过 12 个月。我们之前报道了在α-突触核蛋白原纤维注射后 1 到 12 个月内α-突触核蛋白聚集体的逐渐扩散,现在报告了在该模型中注射后 18 和 23 个月时病理扩散的程度。我们的数据显示,在 12 到 18 个月之间,在人类和在较小程度上的小鼠α-突触核蛋白原纤维注射后,有更多的大脑区域出现病理。在注射小鼠和人类α-突触核蛋白原纤维 18 和 23 个月后,与 12 个月时相比,我们观察到一些大脑区域的α-突触核蛋白聚集体密度降低。与早期时间点相比,在 23 个月时没有其他大脑区域出现α-突触核蛋白聚集体。此外,我们还证明,诱导的α-突触核蛋白病在前嗅核中引发了显著的早期神经元丢失。相比之下,即使在注射后 18 个月,嗅球中的僧帽细胞也没有丢失。我们推测,α-突触核蛋白病理的持续进展缺乏是由于神经元丢失导致的神经回路受损所致,并且可能是由于野生型小鼠中具有弹性的神经元中的蛋白水解机制的激活,这些机制通过降解致病性α-突触核蛋白来平衡传播和播种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54f5/5756266/b1f79ab90157/401_2017_1792_Fig1_HTML.jpg

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