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通过小胶质细胞TYROBP网络,颗粒蛋白前体缺乏对淀粉样蛋白和tau病理的相反作用。

Opposing effects of progranulin deficiency on amyloid and tau pathologies via microglial TYROBP network.

作者信息

Takahashi Hideyuki, Klein Zoe A, Bhagat Sarah M, Kaufman Adam C, Kostylev Mikhail A, Ikezu Tsuneya, Strittmatter Stephen M

机构信息

Cellular Neuroscience, Neurodegeneration and Repair Program, Departments of Neurology and Neurobiology, Yale University School of Medicine, New Haven, CT, 06536, USA.

Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, USA.

出版信息

Acta Neuropathol. 2017 May;133(5):785-807. doi: 10.1007/s00401-017-1668-z. Epub 2017 Jan 9.

Abstract

Progranulin (PGRN) is implicated in Alzheimer's disease (AD) as well as frontotemporal lobar degeneration. Genetic studies demonstrate an association of the common GRN rs5848 variant that results in reduced PGRN levels with increased risk for AD. However, the mechanisms by which PGRN reduction from the GRN AD risk variant or mutation exacerbates AD pathophysiology remain ill defined. Here, we show that the GRN AD risk variant has no significant effects on florbetapir positron emission tomographic amyloid imaging and cerebrospinal fluid (CSF) Aβ levels, whereas it is associated with increased CSF tau levels in human subjects of the Alzheimer's disease neuroimaging initiative studies. Consistent with the human data, subsequent analyses using the APPswe/PS1ΔE9 (APP/PS1) mouse model of cerebral amyloidosis show that PGRN deficiency has no exacerbating effects on Aβ pathology. In contrast and unexpectedly, PGRN deficiency significantly reduces diffuse Aβ plaque growth in these APP/PS1 mice. This protective effect is due, at least in part, to enhanced microglial Aβ phagocytosis caused by PGRN deficiency-induced expression of TYROBP network genes (TNG) including an AD risk factor Trem2. PGRN-deficient APP/PS1 mice also exhibit less severe axonal dystrophy and partially improved behavior phenotypes. While PGRN deficiency reduces these amyloidosis-related phenotypes, other neuronal injury mechanisms are increased by loss of PGRN, revealing a multidimensional interaction of GRN with AD. For example, C1q complement deposition at synapses is enhanced in APP/PS1 mice lacking PGRN. Moreover, PGRN deficiency increases tau AT8 and AT180 pathologies in human P301L tau-expressing mice. These human and rodent data suggest that global PGRN reduction induces microglial TNG expression and increases AD risk by exacerbating neuronal injury and tau pathology, rather than by accelerating Aβ pathology.

摘要

颗粒蛋白前体(PGRN)与阿尔茨海默病(AD)以及额颞叶痴呆有关。遗传学研究表明,常见的GRN rs5848变异与AD风险增加相关,该变异会导致PGRN水平降低。然而,GRN AD风险变异或突变导致的PGRN减少加剧AD病理生理的机制仍不清楚。在此,我们表明,GRN AD风险变异对氟比他哌正电子发射断层扫描淀粉样蛋白成像和脑脊液(CSF)Aβ水平没有显著影响,而在阿尔茨海默病神经影像学计划研究的人类受试者中,它与CSF tau水平升高有关。与人类数据一致,随后使用脑淀粉样血管病APPswe/PS1ΔE9(APP/PS1)小鼠模型进行的分析表明,PGRN缺乏对Aβ病理没有加剧作用。相反且出乎意料的是,PGRN缺乏显著减少了这些APP/PS1小鼠中弥漫性Aβ斑块的生长。这种保护作用至少部分归因于PGRN缺乏诱导的TYROBP网络基因(TNG)表达增强,包括AD风险因子Trem2,从而增强了小胶质细胞对Aβ的吞噬作用。PGRN缺乏的APP/PS1小鼠还表现出较轻的轴突营养不良和部分改善的行为表型。虽然PGRN缺乏减少了这些与淀粉样变性相关的表型,但PGRN的缺失增加了其他神经元损伤机制,揭示了GRN与AD的多维相互作用。例如,在缺乏PGRN的APP/PS1小鼠中,突触处的C1q补体沉积增强。此外,PGRN缺乏增加了表达人P301L tau的小鼠中的tau AT8和AT180病理。这些人类和啮齿动物数据表明,整体PGRN减少通过加剧神经元损伤和tau病理而不是加速Aβ病理来诱导小胶质细胞TNG表达并增加AD风险。

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