致病性 LRRK2 基因突变会导致纹状体视网膜旁中间神经元丧失初级纤毛和 Neurturin。

IF 3.3 2区 生物学 Q1 BIOLOGY Life Science Alliance Pub Date : 2024-11-13 Print Date: 2025-01-01 DOI:10.26508/lsa.202402922
Yu-En Lin, Ebsy Jaimon, Francesca Tonelli, Suzanne R Pfeffer
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引用次数: 0

摘要

与帕金森病相关的 LRRK2 激酶激活突变会阻碍细胞培养和大脑中特定细胞类型中初级纤毛的形成。在对运动控制非常重要的纹状体中,约有一半的星形胶质细胞和胆碱能中间神经元失去了初级纤毛,但占主导地位的中棘神经元却没有。在这里,我们发现小鼠和人类纹状体中具有运动抑制调节功能的副缬白质中间神经元也会失去初级纤毛。没有了纤毛,这些神经元就无法对正常诱导 Patched RNA 表达的声子刺猬信号做出反应,其数量也会减少。此外,小鼠神经胶质细胞系衍生神经营养因子相关的 Neurturin RNA 也显著减少。这些实验强调了蛛网膜依赖性神经保护信号通路中副髓鞘神经元的重要性,并表明 LRRK2 的激活与 Neurturin 生成的减少相关,从而导致对多巴胺神经元的神经保护作用减弱。
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Pathogenic LRRK2 mutations cause loss of primary cilia and Neurturin in striatal parvalbumin interneurons.

Parkinson's disease-associated, activating mutations in the LRRK2 kinase block primary cilium formation in cell culture and in specific cell types in the brain. In the striatum that is important for movement control, about half of astrocytes and cholinergic interneurons, but not the predominant medium spiny neurons, lose their primary cilia. Here, we show that mouse and human striatal parvalbumin interneurons that are inhibitory regulators of movement also lose primary cilia. Without cilia, these neurons are not able to respond to Sonic hedgehog signals that normally induce the expression of Patched RNA, and their numbers decrease. In addition, in mouse, glial cell line-derived neurotrophic factor-related Neurturin RNA is significantly decreased. These experiments highlight the importance of parvalbumin neurons in cilium-dependent, neuroprotective signaling pathways and show that LRRK2 activation correlates with decreased Neurturin production, resulting in less neuroprotection for dopamine neurons.

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来源期刊
Life Science Alliance
Life Science Alliance Agricultural and Biological Sciences-Plant Science
CiteScore
5.80
自引率
2.30%
发文量
241
审稿时长
10 weeks
期刊介绍: Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.
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