As one of the popular healthy edible plants, oats derived exosomes have been found to exert effective effects on brain function and modulate neuroinflammation. Creative Biolabs with years of experience in providing services and products in the exosome field is capable of providing customized solutions for clients to carry out research on oat-derived exosomes.
Isolation of Oat-derived Exosomes
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Biodistribution of oat-derived exosomes. | Oat-derived exosomes were administered orally to mice, and tracer fluorescent signals were detected in the mouse brain, liver, and peripheral blood, suggesting that oat-derived exosomes may be enriched in the brain region by oral administration. |
Exploration of oat-derived exosome targeting of brain cells. |
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Oat-derived exosomes regulated ethanol-induced brain inflammation. |
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Oat-derived exosomes alleviated microglia-mediated neuronal cell injury. | Release of TNFα from ethanol-stimulated microglia induced neuronal cell apoptosis, whereas oat-derived exosome treatment was able to protect neuronal cells by inhibiting the expression of TNFα in ethanol-stimulated microglia and was able to improve memory in a mouse model of ethanol-stimulated brain injury. |
Molecular mechanisms of oat-derived exosome uptake by microglia and avoidance of alcohol-induced brain impairment. |
It was shown that oat-derived exosomes into microglia depend on preferential binding of oat β-glucan to hippocalcin by antibody sequestration and gene-specific knockout means, while the oat exosome's lipid digalactosyldiacylglycerol exerted an inhibitory effect on the binding of β-glucan to dectin-1. β-glucan/hippocalcin further interacts with Rab11a and is recruited into the endosomal circulating compartment, and subsequently dectin-1 is separated from the endosomal circulating compartment to promote dectin-1 sorting into exosomes in a Rab11a-dependent manner, thereby inhibiting dectin-1-mediated subsequent NF-κB activation and proinflammatory cytokine secretion. Oat-derived exosomes avoid the pathogenesis of alcohol-induced brain damage and restore brain memory function through these cascading effects. |
Fig. 1 Oral administration of oat-derived exosomes inhibited ethanol-induced microglia activation in mouse brain.1
Oat-derived exosomes carrying oat β-glucan exhibit lipid-lowering, antioxidant, and inflammation-reducing potential, contributing to the development of new strategies for the treatment of hyperlipidemia-related diseases and alcohol-stimulated neurodegenerative disorders. Creative Biolabs is equipped with advanced exosome research technology platforms to provide reliable services related to oat-derived exosomes to our clients. Please contact us to learn more.
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