Metabolome-wide association study on ABCA7 indicates a role of ceramide metabolism in Alzheimer's disease.

Metabolome-wide association study on ABCA7 indicates a role of ceramide metabolism in Alzheimer's disease.
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DOI:
10.1073/pnas.2206083119
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发表时间:
2022-10-25
影响因子:
11.1
通讯作者:
--
中科院分区:
综合性期刊1区
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--
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通过全基因组关联研究确定的阿尔茨海默病易感性的遗传位点是稳健的;然而,潜在的途径还没有很好地理解。通过整合人类和小鼠模型中的基因组学和代谢组学数据,我们提供的证据表明,ABCA 7是阿尔茨海默病已知的主要基因之一,至少部分通过改变鞘脂代谢和神经酰胺发挥作用,这可能为阿尔茨海默病提供新的治疗机会。全基因组关联研究(GWAS)已经确定了与阿尔茨海默病(AD)风险相关的遗传位点,但它们赋予风险的分子机制在很大程度上是未知的。我们通过超高效液相色谱-质谱法(UPLC-MS)使用非靶向代谢谱(代谢组学)对来自GWAS的AD相关基因座进行了代谢组全关联研究(MWAS)。我们发现乳糖神经酰胺(LacCer)与ABCA 7中AD相关的单核苷酸多态性(SNP)相关(P = 5.0 × 10−5至1.3 × 10−44)。我们发现,血浆LacCer浓度与认知能力相关,基因修饰的LacCer水平与AD风险相关。然后,我们发现,与野生型(WT)相比,Abca 7基因敲除小鼠脑组织中鞘磷脂、神经酰胺和己糖神经酰胺的浓度发生了变化(P = 0.049-1.4 × 10−5),但在淀粉样变性小鼠模型中没有发生变化。此外,小胶质细胞的活化部分地通过诱导鞘氨醇激酶的表达来增加己糖神经酰胺的细胞内浓度,鞘氨醇激酶是一种对鞘脂和神经酰胺合成具有高控制系数的酶。我们的工作表明,由ABCA 7功能变异引起的AD风险至少部分通过神经酰胺介导。调节其代谢或下游信号传导可能为AD提供新的治疗机会。
Genetic loci identified by genome-wide association studies for susceptibility to Alzheimer’s disease are robust; however, the underlying pathways are not well understood. By integrating genomics and metabolomics data in humans and mice models, we provide evidence that ABCA7, one of the main genes known for Alzheimer’s disease, is acting, at least in part, through alteration in sphingolipid metabolism and ceramides, which may offer new therapeutic opportunities for Alzheimer’s disease. Genome-wide association studies (GWASs) have identified genetic loci associated with the risk of Alzheimer’s disease (AD), but the molecular mechanisms by which they confer risk are largely unknown. We conducted a metabolome-wide association study (MWAS) of AD-associated loci from GWASs using untargeted metabolic profiling (metabolomics) by ultraperformance liquid chromatography–mass spectrometry (UPLC-MS). We identified an association of lactosylceramides (LacCer) with AD-related single-nucleotide polymorphisms (SNPs) in ABCA7 (P = 5.0 × 10−5 to 1.3 × 10−44). We showed that plasma LacCer concentrations are associated with cognitive performance and genetically modified levels of LacCer are associated with AD risk. We then showed that concentrations of sphingomyelins, ceramides, and hexosylceramides were altered in brain tissue from Abca7 knockout mice, compared with wild type (WT) (P = 0.049–1.4 × 10−5), but not in a mouse model of amyloidosis. Furthermore, activation of microglia increases intracellular concentrations of hexosylceramides in part through induction in the expression of sphingosine kinase, an enzyme with a high control coefficient for sphingolipid and ceramide synthesis. Our work suggests that the risk for AD arising from functional variations in ABCA7 is mediated at least in part through ceramides. Modulation of their metabolism or downstream signaling may offer new therapeutic opportunities for AD.
DOI: 10.1038/s41588-022-01024-z
发表时间: 2022-04
期刊: NATURE GENETICS
影响因子: 30.8
作者:
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通讯作者: Lambert, Jean-Charles
DOI: 10.1038/ng.507
发表时间: 2010-02
期刊: Nature genetics
影响因子: 30.8
作者:
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DOI: 10.1186/s13742-015-0047-8
发表时间: 2015
期刊: GigaScience
影响因子: 9.2
作者:
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通讯作者: Lee JJ
DOI: 10.1001/archneur.64.9.1323
发表时间: 2007-09-01
影响因子: --
作者:
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发表时间: 2010-09-03
影响因子: 4.4
作者:
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