Department of Neuroscience, Georgetown University Medical Center, 3970 Reservoir Road N.W., Washington, DC, 20007, USA.
Int J Obes (Lond). 2024 Jun;48(6):841-848. doi: 10.1038/s41366-024-01481-y. Epub 2024 Mar 7.
Obesity is the top modifiable risk factor for Alzheimer's disease. We hypothesized that high fat diet (HFD)-induced obesity alters brain transcriptomics in APOE-genotype and sex dependent manners. Here, we investigated interactions between HFD, APOE, and sex, using a knock-in mouse model of the human APOE3 and APOE4 alleles.
Six-month-old APOE3-TR and APOE4-TR mice were treated with either HFD or control chow. After 4 months, total RNA was extracted from the cerebral cortices and analyzed by poly-A enriched RNA sequencing on the Illumina platform.
Female mice demonstrated profound HFD-induced transcriptomic changes while there was little to no effect in males. In females, APOE3 brains demonstrated about five times more HFD-induced transcriptomic changes (399 up-regulated and 107 down-regulated genes) compared to APOE4 brains (30 up-regulated and 60 down-regulated). Unsupervised clustering analysis revealed two gene sets that responded to HFD in APOE3 mice but not in APOE4 mice. Pathway analysis demonstrated that HFD in APOE3 mice affected cortical pathways related to feeding behavior, blood circulation, circadian rhythms, extracellular matrix, and cell adhesion.
Female mice and APOE3 mice have the strongest cortical transcriptomic responses to HFD related to feeding behavior and extracellular matrix remodeling. The relative lack of response of the APOE4 brain to stress associated with obesity may leave it more susceptible to additional stresses that occur with aging and in AD.
肥胖是阿尔茨海默病的最大可改变风险因素。我们假设高脂肪饮食(HFD)引起的肥胖以 APOE 基因型和性别依赖的方式改变大脑转录组。在这里,我们使用人类 APOE3 和 APOE4 等位基因的敲入小鼠模型研究了 HFD、APOE 和性别之间的相互作用。
6 个月大的 APOE3-TR 和 APOE4-TR 小鼠分别用 HFD 或对照饲料处理。4 个月后,从大脑皮质中提取总 RNA,并在 Illumina 平台上进行聚 A 富集 RNA 测序分析。
雌性小鼠表现出明显的 HFD 诱导的转录组变化,而雄性小鼠则几乎没有影响。在雌性小鼠中,与 APOE4 大脑相比,APOE3 大脑显示出约五倍的 HFD 诱导的转录组变化(399 个上调和 107 个下调基因)。无监督聚类分析显示了两组基因,它们对 APOE3 小鼠的 HFD 有反应,但对 APOE4 小鼠没有反应。通路分析表明,APOE3 小鼠的 HFD 影响了与摄食行为、血液循环、昼夜节律、细胞外基质和细胞黏附相关的皮质通路。
雌性小鼠和 APOE3 小鼠对与摄食行为和细胞外基质重塑相关的 HFD 有最强的皮质转录组反应。APOE4 大脑对与肥胖相关的应激反应相对较弱,可能使其更容易受到与衰老和 AD 相关的其他应激的影响。