# Oligodendrocyte precursor cell transplantation attenuates inflammation after ischemic stroke in mice

**Authors:** Li-Ping Wang, Chang Liu, Yuanyuan Ma, Aijuan Yan, Guo-Yuan Yang, Xinkai Qu, Wenshi Wei

PMC · DOI: 10.3389/fneur.2025.1583982 · Frontiers in Neurology · 2025-07-16

## TL;DR

Transplanting oligodendrocyte precursor cells reduces inflammation and protects the blood-brain barrier after stroke in mice.

## Contribution

This study shows that oligodendrocyte precursor cells reduce neuroinflammation and blood-brain barrier disruption after stroke.

## Key findings

- Oligodendrocyte precursor cell transplantation reduced infarct volume and improved neurological recovery.
- Transplanted cells decreased levels of inflammatory cytokines IL-1β, IL-6, and TNF-α.
- β-catenin expression increase mediates anti-inflammatory effects of oligodendrocyte precursor cells.

## Abstract

Disruption of blood–brain barrier and neuroinflammation are critical pathological features in the acute phase of ischemic stroke. This study investigates whether oligodendrocyte precursor cell transplantation can downregulate inflammation to attenuate blood–brain barrier disruption following ischemic brain injury.

Adult male Institute of Cancer Research mice (n = 60) underwent transient middle cerebral artery occlusion. Post ischemic assault, these mice received a stereotactic injection of oligodendrocyte precursor cells (6 × 105). Neurobehavioral outcomes, infarct volume, inflammatory cytokines, myeloperoxidase, and tight junction protein levels were measured following ischemia.

Oligodendrocyte precursor cell transplantation reduced infarct volume, alleviated anxiety and depression, and promoted neurological recovery after ischemic stroke. Compared to the control group, oligodendrocyte precursor cell treated mice exhibited reduced levels of inflammatory cytokines IL-1β, IL-6, and TNF-α, reduced neutrophil infiltration, and diminished loss of tight junction protein. Oligodendrocyte precursor cells alleviated inflammation by increasing β-catenin expression. The administration of β-catenin inhibitor blocked the beneficial effects of oligodendrocyte precursor cell transplantation on neuroinflammation and blood–brain barrier permeability.

This study demonstrates that oligodendrocyte precursor cell transplantation attenuates neuroinflammation and protectes blood–brain barrier in the acute phase of ischemic stroke. Our findings indicate that oligodendrocyte precursor cell transplantation is a promising therapeutic approach for ischemic stroke.

## Linked entities

- **Proteins:** ctnnb1.S (catenin beta 1 S homeolog), IL1B (interleukin 1 beta), IL6 (interleukin 6), TNF (tumor necrosis factor)
- **Diseases:** ischemic stroke (MONDO:1060198)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cspg4 (chondroitin sulfate proteoglycan 4) [NCBI Gene 81651] {aka Ng2}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Vcam1 (vascular cell adhesion molecule 1) [NCBI Gene 22329] {aka CD106, Vcam-1}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, Icam1 (intercellular adhesion molecule 1) [NCBI Gene 15894] {aka CD54, Icam-1, Ly-47, MALA-2}, Rbfox3 (RNA binding fox-1 homolog 3) [NCBI Gene 287847] {aka Hrnbp3, Neun, RGD1560070}, Gfap (glial fibrillary acidic protein) [NCBI Gene 24387], Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Fgf2 (fibroblast growth factor 2) [NCBI Gene 14173] {aka Fgf-2, Fgf2a, Fgfb, bFGF}, Wnt7a (wingless-type MMTV integration site family, member 7A) [NCBI Gene 22421] {aka Wnt-7a, px, tw}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Mbp (myelin basic protein) [NCBI Gene 24547] {aka Mbps}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Aif1 (allograft inflammatory factor 1) [NCBI Gene 29427] {aka BART-1, Bart1, iba1, mrf-1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}
- **Diseases:** anxious behavior (MESH:D001523), Brain infarct (MESH:D020520), neuronal injury (MESH:D009410), multiple sclerosis (MESH:D009103), cerebral ischemia (MESH:D002545), neuroinflammation (MESH:D000090862), Infarct (MESH:D007238), middle cerebral artery occlusion (MESH:D020244), ischemia (MESH:D007511), injury (MESH:D014947), hemorrhagic (MESH:D006470), acute infection (MESH:D000208), brain atrophy (MESH:C566985), Depression (MESH:D003866), brain damage (MESH:D001925), anxiety (MESH:D001007), ischemic injury (MESH:D017202), experimental autoimmune encephalomyelitis (MESH:D004681), death (MESH:D003643), Cancer (MESH:D009369), Inflammation (MESH:D007249), brain injury (MESH:D001930), neurobehavioral deficiency (MESH:D019954), stroke (MESH:D020521), edema (MESH:D004487), ischemic tissue damage (MESH:D017695), BBB (MESH:C536830), inflammatory cytokines (MESH:D000080424), Ischemic stroke (MESH:D002544)
- **Chemicals:** XAV-939 (MESH:C544261), DAPI (MESH:C007293), glutamine (MESH:D005973), DMEM (-), methanol (MESH:D000432), Cresyl violet (MESH:C028911), SE (MESH:D012643), ROS (MESH:D017382), silicone (MESH:D012828), cyclosporine A (MESH:D016572), isoflurane (MESH:D007530), CFDA-SE (MESH:C087165)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307449/full.md

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Source: https://tomesphere.com/paper/PMC12307449