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Land 循环重塑鼠大脑皮质甘油磷酸胆碱过程中的明显紊乱,标志着两种阿尔茨海默病小鼠模型的症状发作和进展。

Distinct disruptions in Land's cycle remodeling of glycerophosphocholines in murine cortex mark symptomatic onset and progression in two Alzheimer's disease mouse models.

机构信息

Neural Regeneration Laboratory, Ottawa Institute of Systems Biology, Centre for Catalysis Research and Innovation, University of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.

Department of Biochemistry, Microbiology, and Immunology, University of Ottawa, Ottawa, ON, Canada.

出版信息

J Neurochem. 2019 May;149(4):499-517. doi: 10.1111/jnc.14560. Epub 2018 Nov 8.

Abstract

Changes in glycerophosphocholine metabolism are observed in Alzheimer's disease; however, it is not known whether these metabolic disruptions are linked to cognitive decline. Here, using unbiased lipidomic approaches and direct biochemical assessments, we profiled Land's cycle lipid remodeling in the hippocampus, frontal cortex, and temporal-parietal-entorhinal cortices of human amyloid beta precursor protein (ΑβPP) over-expressing mice. We identified a cortex-specific hypo-metabolic signature at symptomatic onset and a cortex-specific hyper-metabolic signature of Land's cycle glycerophosphocholine remodeling over the course of progressive behavioral decline. When N5 TgCRND8 and ΑβPP /PSI mice first exhibited deficits in the Morris Water Maze, levels of lyso-phosphatidylcholines, LPC(18:0/0:0), LPC(16:0/0:0), LPC(24:6/0:0), LPC(25:6/0:0), the lyso-platelet-activating factor (PAF), LPC(O-18:0/0:0), and the PAF, PC(O-22:6/2:0), declined as a result of reduced calcium-dependent cytosolic phospholipase A α (cPLA α) activity in all cortices but not hippocampus. Chronic intermittent hypoxia, an environmental risk factor that triggers earlier learning memory impairment in ΑβPP /PSI mice, elicited these same metabolic changes in younger animals. Thus, this lipidomic signature of phenoconversion appears age-independent. By contrast, in symptomatic N5 TgCRND8 mice, cPLA α activity progressively increased; overall Lyso-phosphatidylcholines (LPC) and LPC(O) and PC(O-18:1/2:0) levels progressively rose. Enhanced cPLA α activity was only detected in transgenic mice; however, age-dependent increases in the PAF acetylhydrolase 1b α to α expression ratio, evident in both transgenic and non-transgenic mice, reduced PAF hydrolysis thereby contributing to PAF accumulation. Taken together, these data identify distinct age-independent and age-dependent disruptions in Land's cycle metabolism linked to symptomatic onset and progressive behavioral decline in animals with pre-existing Αβ pathology. OPEN SCIENCE BADGES: This article has received a badge for Open Materials because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.

摘要

阿尔茨海默病患者的甘油磷酸胆碱代谢发生变化;然而,这些代谢紊乱是否与认知能力下降有关尚不清楚。在这里,我们使用无偏脂质组学方法和直接生化评估,对人类淀粉样前体蛋白(ΑβPP)过表达小鼠的海马体、额叶皮质和颞顶-杏仁核皮质中的 Land 循环脂质重塑进行了分析。我们在症状发作时发现了皮质特异性低代谢特征,并在进行性行为衰退过程中发现了 Land 循环甘油磷酸胆碱重塑的皮质特异性高代谢特征。当 N5 TgCRND8 和 ΑβPP/PSI 小鼠首次在 Morris 水迷宫中出现缺陷时,溶血磷脂酰胆碱、LPC(18:0/0:0)、LPC(16:0/0:0)、LPC(24:6/0:0)、LPC(25:6/0:0)、溶血血小板激活因子(PAF)、LPC(O-18:0/0:0)和 PAF、PC(O-22:6/2:0)的水平下降,这是由于所有皮质但海马体中钙依赖性胞质型磷脂酶 Aα(cPLAα)活性降低所致。慢性间歇性低氧是触发 ΑβPP/PSI 小鼠早期学习记忆障碍的环境风险因素,它在年轻动物中引起了相同的代谢变化。因此,这种表型转化的脂质组学特征似乎与年龄无关。相比之下,在有症状的 N5 TgCRND8 小鼠中,cPLAα 活性逐渐增加;总的溶血磷脂酰胆碱(LPC)和 LPC(O)和 PC(O-18:1/2:0)水平逐渐升高。只有在转基因小鼠中才检测到增强的 cPLAα 活性;然而,在转基因和非转基因小鼠中都明显存在的 PAF 乙酰水解酶 1bα 到α表达比率的年龄依赖性增加,降低了 PAF 水解,从而导致 PAF 积累。总之,这些数据表明,在具有预先存在的 Αβ 病理学的动物中,与症状发作和进行性行为下降相关的 Land 循环代谢存在明显的年龄独立和年龄依赖性紊乱。开放科学徽章:本文因提供了在手稿中重现研究的所有相关信息而获得了“开放材料”徽章。本文的完整开放科学披露表格可以在文章末尾找到。有关开放实践徽章的更多信息,请访问 https://cos.io/our-services/open-science-badges/。

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