# Inherent Lipid Composition Abnormalities in Astrocytes Associated with Late-Onset Alzheimer’s Disease (LOAD)

**Authors:** Bruce M. Cohen, Eunjung Koh, Kandice R. Levental, Ilya Levental, Kai-Christian Sonntag

PMC · DOI: 10.3390/cells15060549 · 2026-03-19

## TL;DR

Astrocytes from Alzheimer's patients show reduced cholesterol esters and fatty acids, suggesting these lipid changes may be early signs of the disease.

## Contribution

Identifies inherent lipid abnormalities in astrocytes as potential precursors to late-onset Alzheimer’s disease.

## Key findings

- Astrocytes from LOAD patients show substantial reductions in cholesterol esters.
- Most fatty acids in membrane lipids, including mitochondrial membranes, are reduced in LOAD astrocytes.
- Lipid abnormalities are inherent and may serve as early targets for intervention.

## Abstract

What are the main findings?
There are substantial reductions in cholesterol esters in astrocytes derived from cells of patients with late-onset Alzheimer’s disease (LOAD).Most fatty acids in membrane lipids of these astrocytes, including in mitochondrial membranes, tend to be reduced, with only a few increased.

There are substantial reductions in cholesterol esters in astrocytes derived from cells of patients with late-onset Alzheimer’s disease (LOAD).

Most fatty acids in membrane lipids of these astrocytes, including in mitochondrial membranes, tend to be reduced, with only a few increased.

What are the implications of the main findings?
Because these astrocytes are derived from induced pluripotent stem cell (iPSC) lines, the abnormalities observed are inherent features of the cells and may be the determinants of LOAD.These abnormalities may be targets for interventions that would reduce the risk for LOAD or slow its progression.

Because these astrocytes are derived from induced pluripotent stem cell (iPSC) lines, the abnormalities observed are inherent features of the cells and may be the determinants of LOAD.

These abnormalities may be targets for interventions that would reduce the risk for LOAD or slow its progression.

Lipid abnormalities have been observed in brain, cerebrospinal fluid (CSF), and blood in association with late-onset Alzheimer’s disease (LOAD). It is unknown which of these abnormalities are precursors to LOAD and which are concomitants of illness or its treatment. Inherent abnormalities can be identified in induced pluripotent stem cell (iPSC)-derived brain cells. These cells lack markers associated with aging and environmental exposures. The iPSC lines of patients with LOAD or healthy individuals were differentiated to astrocytes. Astrocytes are crucial to neural activity and health, and altered astrocyte functions are associated with LOAD pathology. Lipidomics analyses were performed on whole-cell and mitochondria-enriched fractions. Large reductions in cholesterol esters (CEs) and imbalances in fatty acids (FAs) were observed in LOAD-associated cells or their mitochondria. There were only modest differences in other lipid classes, including membrane structural lipids. The findings identify abnormalities in CEs, as well as in FAs, as inherent abnormalities and likely precursors to LOAD. These differences implicate mechanisms contributing to disease pathogenesis. Further study may lead to early interventions to prevent or delay LOAD.

## Linked entities

- **Chemicals:** fatty acids (PubChem CID 264)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], B4GALT1 (beta-1,4-galactosyltransferase 1) [NCBI Gene 2683] {aka B4GAL-T1, CDG2D, CLDLFIB, GGTB2, GT1, GTB}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, NPC1 (NPC intracellular cholesterol transporter 1) [NCBI Gene 4864] {aka NPC, POGZ, SLC65A1}, NANOG (Nanog homeobox) [NCBI Gene 79923], VTN (vitronectin) [NCBI Gene 7448] {aka V75, VN, VNT}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, PAX6 (paired box 6) [NCBI Gene 5080] {aka AN, AN1, AN2, ASGD5, D11S812E, FVH1}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, S100B (S100 calcium binding protein B) [NCBI Gene 6285] {aka NEF, S100, S100-B, S100beta}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, BMP4 (bone morphogenetic protein 4) [NCBI Gene 652] {aka BMP2B, BMP2B1, MCOPS6, OFC11, ZYME}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, SLC1A3 (solute carrier family 1 member 3) [NCBI Gene 6507] {aka EA6, EAAT1, GLAST, GLAST1}, SOX1 (SRY-box transcription factor 1) [NCBI Gene 6656], POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460] {aka OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4}, GRDX (Graves disease, susceptibility to, X-linked) [NCBI Gene 117189] {aka GD3}
- **Diseases:** AD (MESH:D000544), brain damage (MESH:D001925), amyloid (MESH:C000718787), Lipid abnormalities (MESH:D011017), inflammation (MESH:D007249), degeneration of cholinergic neurons (MESH:D009410), dementia (MESH:D003704), metabolic abnormality (MESH:D008659), PC (MESH:C535298), FA (MESH:C565561), brain disorders (MESH:D001927), chronic (MESH:D002908), Mental Disorders (MESH:D001523), neuroinflammation (MESH:D000090862), astrocytoma (MESH:D001254), cognitive deficits (MESH:D003072), neurotoxicity (MESH:D020258), damage to the cardiovascular system (MESH:D002318), toxicity (MESH:D064420), neurodegeneration (MESH:D019636), HC (MESH:D000067329), atherosclerosis (MESH:D050197), deficiency (MESH:D007153), mitochondrial dysfunction (MESH:D028361), tangles (MESH:D055956), MCI (MESH:D060825), CL (MESH:C566917), developmental disorders (MESH:D002658), injury to (MESH:D014947)
- **Chemicals:** TWEEN-20 (MESH:D011136), choline (MESH:D002794), PE (MESH:C483858), eicosapentaenoic acid (MESH:D015118), lysophosphatidylinositol (MESH:C025449), propanol (MESH:D000433), acetate (MESH:D000085), glucose (MESH:D005947), ammonium acetate (MESH:C018824), BCA (MESH:C047117), water (MESH:D014867), FFAs (MESH:D005230), PA (MESH:D010712), Glycerophospholipids (MESH:D020404), Polyunsaturated FAs (MESH:D005231), PS (MESH:D010718), PC (MESH:D010713), Gangliosides (MESH:D005732), palmitoleic acid (MESH:C008757), glycosphingolipids (MESH:D006028), DHA (MESH:D004281), Ceramides (MESH:D002518), magnesium (MESH:D008274), PI (MESH:D010716), Arachidonic acid (MESH:D016718), phospholipid (MESH:D010743), acetylcholine (MESH:D000109), DAG (MESH:D004075), LPC (MESH:D008244), methylamine (MESH:C027451), Penicillin (MESH:D010406), Cardiolipin (MESH:D002308), docosanoic acid (MESH:C007547), methanol (MESH:D000432), Sphingolipids (MESH:D013107), CE (MESH:D002788), TBS (MESH:D013725), GM1 (MESH:D005677), omega-3 fatty acid (MESH:D015525), dorsomorphin (MESH:C516138), ammonium (MESH:D064751), sphingomyelin (MESH:D013109), F12 (MESH:C007782), heptadecanoic acid (MESH:C013102), VLCFA (MESH:C017364), GlutaMax (MESH:C054122), SDS (MESH:D012967), nervonic acid (MESH:C013147), Lipid (MESH:D008055), glycerol (MESH:D005990), triacylglycerols (MESH:D014280), eicosenoic acid (MESH:C572289), Cholesterol (MESH:D002784), linoleic acid (MESH:D019787), PG (MESH:D010715), B27 (-), dihexosylceramide (MESH:C012905), Monounsaturated FAs (MESH:D005229), LDN193189 (MESH:C554430), TG (MESH:D013866)
- **Species:** Sendai virus [taxon 11191], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** MAB1259 — Homo sapiens (Human), Mucopolysaccharidosis type IVA, Finite cell line (CVCL_9W80)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13025802/full.md

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Source: https://tomesphere.com/paper/PMC13025802