Aging-associated metabolomic and lipidomic remodeling in mouse brain endothelial cell senescence in vitro

The blood-brain barrier (BBB) declines with age, with endothelial senescence implicated as a contributor, yet its metabolic features remain incompletely defined. We induced senescence in mouse brain endothelial cells (BECs) using the chemotherapeutic doxorubicin and the oxidative stress mediator hydrogen peroxide and performed untargeted mass spectrometry of cell lysates and supernatants. Senescence was confirmed by increased senescence-associated {beta}-galactosidase activity and elevated cyclin-dependent kinase inhibitors p16 and p21, along with increased Il-6 mRNA as senescence-associated secretory phenotype marker. At the BBB structural level, occludin was consistently reduced, ZO-1 decreased with H2O2 (with a similar trend under doxorubicin), and claudin-5 showed a variable, non-significant reduction, indicating target- and inducer-specific junctional remodeling. Pathway mapping highlighted prominent remodeling of lipid metabolism (including glycerophospholipids, sphingolipids, acylcarnitines) and amino-acid pathways, with both shared and inducer-specific shifts. These discovery-stage in vitro results recapitulate several metabolites previously associated with senescence across tissues and nominate additional candidates for hypothesis testing. To increase mechanistic and translational relevance, we outline a staged roadmap: validation in advanced multicellular and flow-based BBB models followed by in vivo studies, with attention to route-specific BBB readouts. Overall, this work provides a curated snapshot of metabolic remodeling in brain endothelial senescence that co-occurs with selective tight-junction alterations relevant to BBB aging. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=75 SRC="FIGDIR/small/670255v2_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@1644442org.highwire.dtl.DTLVardef@1bd5821org.highwire.dtl.DTLVardef@1e4efd5org.highwire.dtl.DTLVardef@13d942d_HPS_FORMAT_FIGEXP M_FIG C_FIG Mouse brain endothelial cells exposed to doxorubicin (Dox) or hydrogen peroxide (H2O2) underwent senescence ({uparrow}SA-{beta}-gal activity, p16/p21 expression), accompanied by selective reductions in tight-junction proteins. Untargeted mass spectrometry profiled metabolites in cell lysates and supernatants. Lipids, followed by amino acid metabolites, comprised the largest share of alterations, highlighting these pathways as major components of metabolic reprogramming associated in endothelial senescence.