脂类学
小胶质细胞
脂质体
星形胶质细胞
生物
神经科学
代谢组学
诱导多能干细胞
脂质代谢
计算生物学
神经炎症
电池类型
细胞
生物信息学
免疫学
炎症
中枢神经系统
基因
生物化学
胚胎干细胞
作者
Femke M. Feringa,Sascha J. Koppes-den Hertog,Li-Chiao Wang,Rico J. E. Derks,Iris Kruijff,Lena Erlebach,Jorin Heijneman,Ricardo Miramontes,Nadine Pömpner,Niek Blomberg,Damien Olivier‐Jimenez,Lill Eva Johansen,Alexander J. Cammack,Ashling Giblin,Christina E. Toomey,Indigo V.L. Rose,Hebao Yuan,Michael E. Ward,Adrian M. Isaacs,Martin Kampmann
标识
DOI:10.1038/s42255-025-01365-z
摘要
Abstract Lipid alterations in the brain have been implicated in many neurodegenerative diseases. To facilitate comparative lipidomic research across brain diseases, we establish a data common named the Neurolipid Atlas that we prepopulated with isogenic induced pluripotent stem cell (iPS cell)-derived lipidomics data for different brain diseases. Additionally, the resource contains lipidomics data of human and mouse brain tissue. Leveraging multiple datasets, we demonstrate that iPS cell-derived neurons, microglia and astrocytes exhibit distinct lipid profiles that recapitulate in vivo lipotypes. Notably, the Alzheimer disease (AD) risk gene ApoE4 drives cholesterol ester (CE) accumulation specifically in human astrocytes and we also observe CE accumulation in whole-brain lipidomics from persons with AD. Multiomics interrogation of iPS cell-derived astrocytes revealed that altered cholesterol metabolism has a major role in astrocyte immune pathways such as the immunoproteasome and major histocompatibility complex class I antigen presentation. Our data commons, available online ( https://neurolipidatlas.com/ ), allows for data deposition by the community and provides a user-friendly tool and knowledge base for a better understanding of lipid dyshomeostasis in neurodegenerative diseases.
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