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颗粒蛋白前体缺陷小鼠和额颞叶痴呆伴GRN突变患者细胞外囊泡水平升高。

Elevated levels of extracellular vesicles in progranulin-deficient mice and FTD-GRN Patients.

作者信息

Arrant Andrew E, Davis Skylar E, Vollmer Rachael M, Murchison Charles F, Mobley James A, Nana Alissa L, Spina Salvatore, Grinberg Lea T, Karydas Anna M, Miller Bruce L, Seeley William W, Roberson Erik D

机构信息

Departments of Neurology and Neurobiology, Center for Neurodegeneration and Experimental Therapeutics, Alzheimer's Disease Center, Evelyn F. McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

Ann Clin Transl Neurol. 2020 Dec;7(12):2433-2449. doi: 10.1002/acn3.51242. Epub 2020 Nov 16.

Abstract

OBJECTIVE

The goal of this study was to investigate the effect of progranulin insufficiency on extracellular vesicles (EVs), a heterogeneous population of vesicles that may contribute to progression of neurodegenerative disease. Loss-of-function mutations in progranulin (GRN) are a major cause of frontotemporal dementia (FTD), and brains from GRN carriers with FTD (FTD-GRN) exhibit signs of lysosomal dysfunction. Lysosomal dysfunction may induce compensatory increases in secretion of exosomes, EVs secreted from the endolysosomal system, so we hypothesized that progranulin insufficiency would increase EV levels in the brain.

METHODS

We analyzed levels and protein contents of brain EVs from Grn mice, which model the lysosomal abnormalities of FTD-GRN patients. We then measured brain EVs in FTD-GRN patients. To assess the relationship of EVs with symptomatic disease, we measured plasma EVs in presymptomatic and symptomatic GRN mutation carriers.

RESULTS

Grn mice had elevated brain EV levels and altered EV protein contents relative to wild-type mice. These changes were age-dependent, occurring only after the emergence of pathology in Grn mice. FTD-GRN patients (n = 13) had elevated brain EV levels relative to controls (n = 5). Symptomatic (n = 12), but not presymptomatic (n = 7), GRN carriers had elevated plasma EV levels relative to controls (n = 8).

INTERPRETATION

These data show that symptomatic FTD-GRN patients have elevated levels of brain and plasma EVs, and that this effect is modeled in the brain of Grn mice after the onset of pathology. This increase in EVs could influence FTD disease progression, and provides further support for EVs as potential FTD biomarkers.

摘要

目的

本研究的目的是调查颗粒蛋白前体不足对细胞外囊泡(EVs)的影响,细胞外囊泡是一类异质性囊泡群体,可能与神经退行性疾病的进展有关。颗粒蛋白前体(GRN)功能丧失突变是额颞叶痴呆(FTD)的主要病因,携带FTD的GRN突变患者(FTD-GRN)的大脑表现出溶酶体功能障碍的迹象。溶酶体功能障碍可能会诱导内溶酶体系统分泌的外泌体(一种细胞外囊泡)代偿性增加,因此我们推测颗粒蛋白前体不足会增加大脑中的细胞外囊泡水平。

方法

我们分析了Grn小鼠脑内细胞外囊泡的水平和蛋白质含量,Grn小鼠可模拟FTD-GRN患者的溶酶体异常。然后我们测量了FTD-GRN患者脑内的细胞外囊泡。为了评估细胞外囊泡与症状性疾病的关系,我们测量了症状前和症状性GRN突变携带者血浆中的细胞外囊泡。

结果

与野生型小鼠相比,Grn小鼠脑内细胞外囊泡水平升高,且细胞外囊泡蛋白质含量发生改变。这些变化与年龄有关,仅在Grn小鼠出现病理变化后才发生。与对照组(n = 5)相比,FTD-GRN患者(n = 13)脑内细胞外囊泡水平升高。与对照组(n = 8)相比,有症状的(n = 12)而非症状前的(n = 7)GRN携带者血浆中的细胞外囊泡水平升高。

解读

这些数据表明,有症状的FTD-GRN患者脑内和血浆中的细胞外囊泡水平升高,并且在病理变化发生后,Grn小鼠的大脑中也出现了这种效应。细胞外囊泡的这种增加可能会影响FTD疾病的进展,并进一步支持细胞外囊泡作为潜在的FTD生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/251f/7732244/bd3e05d3704b/ACN3-7-2433-g001.jpg

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