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药理学干扰揭示了 Thap1 基因敲除小鼠中 D2 受体反应的缺陷。

Pharmacological perturbation reveals deficits in D2 receptor responses in Thap1 null mice.

机构信息

Ken and Ruth Davee Department of Neurology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, 60611, USA.

Northwestern University Interdepartmental Neuroscience Program, Northwestern University, Evanston, Illinois, 60208, USA.

出版信息

Ann Clin Transl Neurol. 2021 Dec;8(12):2302-2308. doi: 10.1002/acn3.51481. Epub 2021 Nov 21.

DOI:10.1002/acn3.51481
PMID:34802187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8670318/
Abstract

The primary dystonia DYT6 is caused by mutations in the transcription factor Thanatos-associated protein 1 (THAP1). To understand THAP1's functions, we generated mice lacking THAP1 in the nervous system. THAP1 loss causes locomotor deficits associated with transcriptional changes. Since many of the genes misregulated involve dopaminergic signaling, we pharmacologically challenged the two striatal canonical dopamine pathways: the direct, regulated by the D1 receptor, and the indirect, regulated by the D2 receptor. We discovered that depleting THAP1 specifically interferes with the D2 receptor responses, pointing to a selective misregulation of the indirect pathway in DYT6 with implications for pathogenesis and treatment.

摘要

原发性肌张力障碍 DYT6 是由转录因子Thanatos 相关蛋白 1 (THAP1) 的突变引起的。为了了解 THAP1 的功能,我们在神经系统中生成了缺乏 THAP1 的小鼠。THAP1 的缺失导致运动缺陷,同时伴有转录变化。由于许多失调的基因涉及多巴胺能信号,我们用药物挑战了两个纹状体的经典多巴胺通路:直接通路,受 D1 受体调节;间接通路,受 D2 受体调节。我们发现,特异性耗尽 THAP1 会干扰 D2 受体的反应,这表明 DYT6 中的间接通路存在选择性失调,这对发病机制和治疗有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4a4/8670318/5e49390e51ca/ACN3-8-2302-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4a4/8670318/dab4c11166b9/ACN3-8-2302-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4a4/8670318/5e49390e51ca/ACN3-8-2302-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4a4/8670318/dab4c11166b9/ACN3-8-2302-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4a4/8670318/5e49390e51ca/ACN3-8-2302-g001.jpg

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J Neurosci. 2019 Sep 4;39(36):7195-7205. doi: 10.1523/JNEUROSCI.0407-19.2019. Epub 2019 Jul 18.
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Dystonia genes and their biological pathways.肌张力障碍基因及其生物学途径。
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Heterozygous Gnal Mice Are a Novel Animal Model with Which to Study Dystonia Pathophysiology.杂合子Gnal小鼠是用于研究肌张力障碍病理生理学的新型动物模型。
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