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抑制 Nemo 样激酶可增加溶酶体生物发生并改善 TDP-43 相关的神经退行性变。

Reduction of nemo-like kinase increases lysosome biogenesis and ameliorates TDP-43-related neurodegeneration.

机构信息

Interdepartmental Neuroscience Program.

Department of Neuroscience, and.

出版信息

J Clin Invest. 2023 Aug 15;133(16):e138207. doi: 10.1172/JCI138207.

Abstract

Protein aggregation is a hallmark of many neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS). Although mutations in TARDBP, encoding transactive response DNA-binding protein 43 kDa (TDP-43), account for less than 1% of all ALS cases, TDP-43-positive aggregates are present in nearly all ALS patients, including patients with sporadic ALS (sALS) or carrying other familial ALS-causing (fALS-causing) mutations. Interestingly, TDP-43 inclusions are also present in subsets of patients with frontotemporal dementia, Alzheimer's disease, and Parkinson's disease; therefore, methods of activating intracellular protein quality control machinery capable of clearing toxic cytoplasmic TDP-43 species may alleviate disease-related phenotypes. Here, we identify a function of nemo-like kinase (Nlk) as a negative regulator of lysosome biogenesis. Genetic or pharmacological reduction of Nlk increased lysosome formation and improved clearance of aggregated TDP-43. Furthermore, Nlk reduction ameliorated pathological, behavioral, and life span deficits in 2 distinct mouse models of TDP-43 proteinopathy. Because many toxic proteins can be cleared through the autophagy/lysosome pathway, targeted reduction of Nlk represents a potential approach to therapy development for multiple neurodegenerative disorders.

摘要

蛋白质聚集是许多神经退行性疾病的标志,包括肌萎缩侧索硬化症(ALS)。虽然编码反式激活反应 DNA 结合蛋白 43kDa(TDP-43)的 TARDBP 突变占所有 ALS 病例的比例不到 1%,但 TDP-43 阳性聚集体几乎存在于所有 ALS 患者中,包括散发性 ALS(sALS)或携带其他家族性 ALS 致病(fALS-causing)突变的患者。有趣的是,TDP-43 包含物也存在于额颞叶痴呆、阿尔茨海默病和帕金森病患者的亚组中;因此,激活能够清除有毒细胞质 TDP-43 物质的细胞内蛋白质质量控制机制的方法可能减轻与疾病相关的表型。在这里,我们确定了 Nemo 样激酶(Nlk)作为溶酶体生物发生的负调节剂的功能。Nlk 的遗传或药理学减少增加了溶酶体的形成并改善了聚集的 TDP-43 的清除。此外,Nlk 减少改善了 2 种不同的 TDP-43 蛋白病小鼠模型的病理、行为和寿命缺陷。由于许多毒性蛋白质可以通过自噬/溶酶体途径清除,因此靶向减少 Nlk 代表了多种神经退行性疾病治疗开发的潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc9/10425213/ee2fd53982bd/jci-133-138207-g004.jpg

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