# Mesenchymal stem cell membrane-coated kaempferol biomimetic nanoformulation for the treatment of atherosclerosis

**Authors:** Qianting Zhang, Xiangxiu Wang, Hongping Zhang, Keqiao He, Daojun Pu, Hong Chen, Anna Malashicheva, Wenbo Han, Chuanrong Zhao, Guixue Wang

PMC · DOI: 10.1063/5.0303756 · APL Bioengineering · 2026-02-26

## TL;DR

Researchers developed a new nano-drug delivery system using mesenchymal stem cell membranes to target atherosclerotic sites and reduce plaque buildup.

## Contribution

This is the first report of using mesenchymal stem cell membranes to encapsulate kaempferol for treating atherosclerosis.

## Key findings

- Modified MSCM-encapsulated kaempferol nanoparticles specifically target endothelial cells in inflammatory environments.
- Intravenous injection of the nanoparticles reduced lipid plaque load and improved plaque structure in a mouse model.
- The nanoparticles showed biosafety with no significant effects on blood count, lipid balance, or organ function.

## Abstract

Atherosclerosis and its complications are highly prevalent worldwide, and managing oxidative stress in endothelial cells to alleviate abnormal inflammatory damage is a critical therapeutic approach. Nanomedicine delivery systems offer promising solutions by overcoming the limitations of surgical interventions and the off-target effects of oral drugs. In this study, we developed a modified mesenchymal stem cell membrane (MSCM)-encapsulated nanoparticle drug delivery system that effectively delivers kaempferol to atherosclerotic sites. These biomimetic nanoparticles were able to specifically target endothelial cells in an inflammatory environment while evading macrophage-mediated endocytosis. Moreover, the modified MSCM-encapsulated kaempferol nanoparticles (KPM) had a protective effect on oxidatively damaged endothelial cells. In vivo, the modified nanoparticles successfully migrated toward atherosclerotic lesions, as demonstrated in a mouse model of susceptible atherosclerotic plaques. Intravenous injection of KPM significantly reduced the lipid plaque load and improved plaque structure. Furthermore, the biosafety of KPM was comprehensively assessed both in vitro and in vivo, with no significant effects on blood count, lipid balance, cellular activity, body weight, or liver or kidney function. This is the first report of the use of MSCM to encapsulate kaempferol nanodrugs to treat atherosclerosis. This strategy presents a novel and effective therapeutic system for targeted delivery of antioxidant therapy to atherosclerotic sites, offering potential for the treatment of atherosclerosis in cardio-cerebrovascular diseases.

## Linked entities

- **Chemicals:** kaempferol (PubChem CID 5280863)
- **Diseases:** atherosclerosis (MONDO:0005311)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, B3gnt9 (UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9) [NCBI Gene 97440] {aka 3-Gn-T9, B3gnt9-ps, BGnT-9, beta-1, beta3Gn-T9}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Cd47 (CD47 antigen (Rh-related antigen, integrin-associated signal transducer)) [NCBI Gene 16423] {aka 9130415E20Rik, B430305P08Rik, IAP, Itgp}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, Cd44 (CD44 antigen) [NCBI Gene 12505] {aka HERMES, Ly-24, Pgp-1}, Cxcl12 (C-X-C motif chemokine ligand 12) [NCBI Gene 20315] {aka Pbsf, Scyb12, Sdf1, Tlsf, Tpar1}, Cd68 (CD68 antigen) [NCBI Gene 12514] {aka Lamp4, Scard1, gp110}, Cxcr4 (C-X-C motif chemokine receptor 4) [NCBI Gene 12767] {aka CD184, CXC-R4, CXCR-4, Cmkar4, LESTR, PB-CKR}, Acta2 (actin alpha 2, smooth muscle, aorta) [NCBI Gene 11475] {aka 0610041G09Rik, Actvs, SMAalpha, SMalphaA, a-SMA, alphaSMA}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, Gpx4 (glutathione peroxidase 4) [NCBI Gene 625249] {aka GPx-4, GSHPx-4, PHGPx, mtPHGPx, snGPx}
- **Diseases:** MSCM (MESH:D015433), proinflammatory cytokines (MESH:D000080424), feeding disorders (MESH:D001068), stroke (MESH:D020521), necrosis (MESH:D009336), Hemolysis (MESH:D006461), inflammation (MESH:D007249), metastasis (MESH:D009362), AS (MESH:D050197), Alzheimer's disease (MESH:D000544), cancer (MESH:D009369), endothelial dysfunction (MESH:D014652), weight loss (MESH:D015431), Toxicity (MESH:D064420), cardio-cerebrovascular diseases (MESH:D002561)
- **Chemicals:** water (MESH:D014867), CCK8 (MESH:D012844), Kae (MESH:C006552), CO2 (MESH:D002245), DCFH-DA (MESH:C029569), Lipid (MESH:D008055), paraformaldehyde (MESH:C003043), LPS (MESH:D008070), TB (MESH:D013725), ORO (MESH:C011049), alphaMEM (MESH:C420642), colchicine (MESH:D003078), eosin (MESH:D004801), PLGA (MESH:D000077182), hydrochloric acid (MESH:D006851), alkaloids (MESH:D000470), SDS (MESH:D012967), copper (MESH:D003300), alcohol (MESH:D000438), PVDF (MESH:C024865), DP (MESH:D004176), toluidine blue (MESH:D014048), DMSO (MESH:D004121), DAPI (MESH:C007293), flavonoid (MESH:D005419), ROS (MESH:D017382), glycosides (MESH:D006027), fat (MESH:D005223), H2O2 (MESH:D006861), ADPM (-), HE (MESH:D006371), NaCl (MESH:D012965), K (MESH:D011188), hematoxylin (MESH:D006416), PVA (MESH:D011142), xylene (MESH:D014992), polysaccharides (MESH:D011134), nitrogen (MESH:D009584), phosphotungstic acid (MESH:D010772), EDTA (MESH:D004492), ADP (MESH:D000244), MDA (MESH:D008315), oil (MESH:D009821), polyacrylamide (MESH:C016679), carbon (MESH:D002244), rapamycin (MESH:D020123), DPM (MESH:C064754)
- **Species:** Zingiber officinale (ginger, species) [taxon 94328], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), A7R5 — Rattus norvegicus (Rat), Spontaneously immortalized cell line (CVCL_0137), EC — Oncorhynchus tshawytscha (Chinook salmon), Spontaneously immortalized cell line (CVCL_DG46), HUVEC — Homo sapiens (Human), Finite cell line (CVCL_3722)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12948443/full.md

## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948443/full.md

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Source: https://tomesphere.com/paper/PMC12948443