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Tet2缺失和纤毛生成增强可抑制α-突触核蛋白病变。

Tet2 loss and enhanced ciliogenesis suppress α-synuclein pathology.

作者信息

Quansah Emmanuel, Vatsa Naman, Ensink Elizabeth, Brown Jaycie, Cave Tyce, Aguileta Miguel, Schulz Emily, Lindquist Allison, Gilliland Carla, Steiner Jennifer A, Escobar Galvis Martha L, Milčiūtė Milda, Henderson Michael X, Brundin Patrik, Brundin Lena, Marshall Lee L, Gordevicius Juozas

机构信息

Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.

Department of Physiology, Michigan State University, East Lansing, MI, 48824, USA.

出版信息

Acta Neuropathol Commun. 2025 Apr 7;13(1):71. doi: 10.1186/s40478-025-01988-z.

Abstract

There are no approved treatments that slow Parkinson's disease (PD) progression and therefore it is important to identify novel pathogenic mechanisms that can be targeted. Loss of the epigenetic marker, Tet2 appears to have some beneficial effects in PD models, but the underlying mechanism of action is not well understood. We performed an unbiased transcriptomic analysis of cortical neurons isolated from patients with PD to identify dysregulated pathways and determine their potential contributions to the disease process. We discovered that genes associated with primary cilia, non-synaptic sensory and signaling organelles, are upregulated in both early and late stage PD patients. Enhancing ciliogenesis in primary cortical neurons via sonic hedgehog signaling suppressed the accumulation of α-synuclein pathology in vitro. Interestingly, deletion of Tet2 in mice also enhanced the expression of primary cilia and sonic hedgehog signaling genes and reduced the accumulation of α-synuclein pathology and dopamine neuron degeneration in vivo. Our findings demonstrate the crucial role of TET2 loss in regulating ciliogenesis and potentially affecting the progression of PD pathology.

摘要

目前尚无经批准的可减缓帕金森病(PD)进展的治疗方法,因此确定可作为靶点的新致病机制非常重要。表观遗传标记Tet2的缺失似乎在PD模型中具有一些有益作用,但其潜在作用机制尚不清楚。我们对从PD患者分离出的皮质神经元进行了无偏转录组分析,以识别失调的通路并确定它们对疾病进程的潜在影响。我们发现,与初级纤毛、非突触感觉和信号细胞器相关的基因在早期和晚期PD患者中均上调。通过音猬因子信号增强原代皮质神经元的纤毛发生,可在体外抑制α-突触核蛋白病理的积累。有趣的是,小鼠中Tet2的缺失也增强了初级纤毛和音猬因子信号基因的表达,并减少了体内α-突触核蛋白病理的积累和多巴胺神经元变性。我们的研究结果证明了TET2缺失在调节纤毛发生以及潜在影响PD病理进展中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f364/11974201/8c5d0fc1b858/40478_2025_1988_Fig1_HTML.jpg

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