Extended Data Fig. 8: Lipidomics companion to the decrease in MFSD2A expression in the aged brain vasculature. | Nature

Extended Data Fig. 8: Lipidomics companion to the decrease in MFSD2A expression in the aged brain vasculature.

From: Physiological blood–brain transport is impaired with age by a shift in transcytosis

Extended Data Fig. 8

a, PC analysis plot of brain microvessel lipidomes from young (3 mo) and aged (20 mo) mice. There were 25 lipids significantly upregulated and 33 lipids downregulated with age (n = 4, each n is a pool of 4 mice (16 young and 16 aged total), FDR-corrected q < 0.05, Permutation-based FDR of two-sided t-test). b, Absolute abundance (concentrations) of measured microvessel lipid classes with age (n = 4, each n is a pool of 4 mice, Benjamini, Krieger and Yekutieli FDR-corrected two-sided t-test; mean ± s.e.m.). DG is not listed as only one DG species was detected. c, Mole % of MFSD2A-regulated phospholipids19 (PC, PE, PS and LPE) across and within phospholipid classes. Concentrations of individual lipid species were derived with spike-in standards and presented as a quantitative mole % of DHA fatty acid (FA) of all fatty acids in the given class68 or across PC, PE, PS and LPE classes (right, ‘Combined’) (n = 4, each n is a pool of 4 mice, two-sided t-test; mean ± s.e.m.). d, Hierarchical clustering of lipids (by concentration) of microvessels from young (3 mo) and aged (20 mo) mice (n = 4; each sample is a pool of 4 mice) normalized by Z-score. All lipids differentially abundant with an FDR-corrected q < 0.1 are shown (permutation-based FDR of two-sided t-test), and MFSD2A-regulated DHA-phospholipids are labelled.

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