Therapeutic potential of microglia-derived extracellular vesicles in ischemic stroke DOI
Bo Yan, Pan Liao,

Yaru Liu

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 139, P. 112712 - 112712

Published: July 19, 2024

Language: Английский

Apelin-13/APJ promotes neural stem cells to repair ischemic stroke DOI Creative Commons
Shuangmei Li,

Shihan Yuan,

Shujun Yang

et al.

Tissue and Cell, Journal Year: 2025, Volume and Issue: 95, P. 102872 - 102872

Published: March 22, 2025

Neural stem cell therapy is considered as a promising new for ischemic stroke. However, the therapeutic efficacy of neural cells (NSCs) hampered by effects cerebral ischemia and hypoxia, resulting in suboptimal performance. Drug stimulation can further improve NSCs stroke, among which small molecule peptide Apelin-13 could have potential. In this study, we simulated anoxic microenvironment oxygen-glucose deprivation (OGD) to observe improvement on treatment-related functions. Six hours OGD treatment suppressed viability NSCs, while 100 nM mitigated suppression. Additionally, reduced migration capability but enhanced ability under conditions. also increased rate apoptotic decreased ratio Bcl-2 Bax. environment, BDNF expression was elevated, level. APJ endogenous receptor Apelin-13. We knocked down observed that effect abolished environment compared with negative control group knockdown, upregulation brain derived neurotrophic factor (BDNF) lost. Our study found enhances fosters migration, diminishes apoptosis, augments conditions through receptor. The Apelin-13/APJ system may play beneficial role activating purpose treating This positive be mediated downstream effector protein, BDNF.

Language: Английский

Citations

1

Human neural stem cell-derived exosomes activate PINK1/Parkin pathway to protect against oxidative stress-induced neuronal injury in ischemic stroke DOI Creative Commons
Mengke Zhao, Jiayi Wang,

Shuaiyu Zhu

et al.

Journal of Translational Medicine, Journal Year: 2025, Volume and Issue: 23(1)

Published: April 5, 2025

Mitochondria play a critical role in oxidative stress (OS)-induced neuronal injury during ischemic stroke (IS), making them promising therapeutic targets. Mounting evidence underscores the extraordinary promise of exosomes derived from human neural stem cells (hNSCs) management central nervous system (CNS) diseases. Nonetheless, precise mechanisms by which these target mitochondria to ameliorate effects IS remain only partially elucidated. This study investigates protective hNSC (hNSC-Exos) on damage. Using rat model middle cerebral artery occlusion (MCAO) vivo and OS-induced HT22 vitro. Firstly, our research group independently isolated subsequently prepared hNSC-Exos. In vivo, MCAO rats were restored blood flow perfusion simulate ischemia-reperfusion injury, hNSC-Exos injected through stereotaxic injection into brain. Subsequently, evaluated, including histological studies, behavioral assessments. H2O2 was used OS environment MCAO, then its evaluated co-culturing with hNSC-Exos, immunofluorescence staining, western blotting (WB), quantitative real time PCR (qRT-PCR). process exploring specific mechanisms, we utilized RNA sequencing (RNA-seq) detect potential induction mitophagy cells. Afterwards, employed series mitochondrial function assessments autophagy related detection techniques, measuring membrane potential, reactive oxygen species (ROS) levels, transmission electron microscopy (TEM) imaging, monodansylcadaverine (MDC) mCherry-GFP-LC3B staining. addition, further investigated regulatory pathway using inhibitor mdivi-1 knocking out PTEN induced kinase 1 (PINK1) Administration significantly ameliorated brain tissue damage enhanced outcomes rats. treatment led reduction apoptosis facilitated normalization impaired neurogenesis neuroplasticity. Notably, application vitro resulted an upregulation cells, thereby remedying dysfunction. We demonstrate that activate via PINK1/Parkin pathway, improving reducing apoptosis. These findings suggest alleviate regulating pathway. reveals novel cell-derived therapy promoting neuroprotection their as approach for OS-associated CNS diseases, IS.

Language: Английский

Citations

1

Neuroprotective effect of small extracellular vesicle-mediated targeting of AMPKα2 in cerebral ischemia DOI Creative Commons
Alberto Ouro,

Amanda Rodríguez-Díaz,

Tania López-González

et al.

Metabolism, Journal Year: 2025, Volume and Issue: unknown, P. 156160 - 156160

Published: Feb. 1, 2025

Language: Английский

Citations

0

The Role of Exosomes Derived from Various Sources in Facilitating the Healing of Chronic Refractory Wounds DOI Creative Commons

Fengdan Xu,

Qiling Zhang, Yuling Liu

et al.

Pharmacological Research, Journal Year: 2025, Volume and Issue: unknown, P. 107753 - 107753

Published: April 1, 2025

Chronic refractory wounds (CRWs) represent a common and challenging issue in clinical practice, including diabetic foot ulcers, pressure venous arterial ulcers. These significantly impact patients' quality of life may lead to severe consequences such as amputation. Their treatment requires comprehensive consideration both the patient's overall physical condition local wound situation. The major challenges include complex pathogenesis, long cycle, high recurrence rate, heavy economic on patients. Exosomes an emerging therapeutic modality with characteristics low immunogenicity, good biostability, targeting efficiency diseases. derived from different sources exhibit heterogeneity, demonstrating their respective advantages unique properties treatment. This article delves into potential applications mechanisms action exosomes various CRWs, aiming provide new perspectives ideas for management wounds.

Language: Английский

Citations

0

Therapeutic potential of microglia-derived extracellular vesicles in ischemic stroke DOI
Bo Yan, Pan Liao,

Yaru Liu

et al.

International Immunopharmacology, Journal Year: 2024, Volume and Issue: 139, P. 112712 - 112712

Published: July 19, 2024

Language: Английский

Citations

1