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| Main Authors: | , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
ACS biomaterials science & engineering
2025
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| Subjects: | |
| Online Access: | https://pubmed.ncbi.nlm.nih.gov/40396567/ |
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| _version_ | 1868266201718718464 |
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| author | Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao |
| author_facet | Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao |
| collection | PubMed - marine biology |
| contents | Utilizing Extracellular Vesicles from as a Novel Approach for Protecting the Skin from Oxidative Damage. Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao Extracellular Vesicles Animals Oxidative Stress Humans Mice Ultraviolet Rays Skin Hydrogen Peroxide HaCaT Cells Diatoms Antioxidants Reactive Oxygen Species Oxidative stress is a principal factor contributing to skin damage induced by deleterious stimuli, including ultraviolet (UV) radiation. Microalgae-derived extracellular vesicles (EVs), particularly those from (PTEV), are gaining recognition as a potential therapeutic avenue for restoring skin homeostasis, owing to their scalable production and multifaceted biological activities. This study evaluates the therapeutic effects of PTEV on oxidative damage in HO-stimulated HaCaT cells and UV-exposed KM mouse models, based on the extraction and characterization of PTEV. Subsequently, the oxidative stress injury model of HaCaT cells induced by HO and the acute photodamage model of KM mice skin induced by UV were established. The results show that HaCaT cells exhibit a time-dependent uptake of PTEV, confirming that PTEV is nontoxic and has the potential for intercellular cross-boundary regulation. Treatment with PTEV can enhance the vitality of HO-stimulated HaCaT cells, reduce intracellular ROS levels, and increase antioxidant enzyme activity in the cells. Further evaluation revealed that PTEV can inhibit UV-induced thickening of the epidermis and degradation of collagen fibers in mice by suppressing the overexpression of matrix metalloproteinase (MMP-3) induced by UV. It enhances the expression of type I collagen (COL1A1) and increases the activity of antioxidant enzymes, as well as the overall antioxidant capacity of tissues. Additionally, PTEV reduces the increase in malondialdehyde levels and lowers the expression levels of inflammatory factors TNF-α and IL-6, thereby protecting the skin barrier and function in mice with acute photodamage. Continuous production of PTEV offers promising applications in therapeutic strategies. |
| format | Artículo científico |
| id | pubmed_40396567 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | ACS biomaterials science & engineering |
| record_format | pubmed |
| spellingShingle | Utilizing Extracellular Vesicles from as a Novel Approach for Protecting the Skin from Oxidative Damage. Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao Extracellular Vesicles Animals Oxidative Stress Humans Mice Ultraviolet Rays Skin Hydrogen Peroxide HaCaT Cells Diatoms Antioxidants Reactive Oxygen Species Utilizing Extracellular Vesicles from as a Novel Approach for Protecting the Skin from Oxidative Damage. Xu, Ran Lu, Ying Cai, Luyun Zhang, Litao Extracellular Vesicles Animals Oxidative Stress Humans Mice Ultraviolet Rays Skin Hydrogen Peroxide HaCaT Cells Diatoms Antioxidants Reactive Oxygen Species Oxidative stress is a principal factor contributing to skin damage induced by deleterious stimuli, including ultraviolet (UV) radiation. Microalgae-derived extracellular vesicles (EVs), particularly those from (PTEV), are gaining recognition as a potential therapeutic avenue for restoring skin homeostasis, owing to their scalable production and multifaceted biological activities. This study evaluates the therapeutic effects of PTEV on oxidative damage in HO-stimulated HaCaT cells and UV-exposed KM mouse models, based on the extraction and characterization of PTEV. Subsequently, the oxidative stress injury model of HaCaT cells induced by HO and the acute photodamage model of KM mice skin induced by UV were established. The results show that HaCaT cells exhibit a time-dependent uptake of PTEV, confirming that PTEV is nontoxic and has the potential for intercellular cross-boundary regulation. Treatment with PTEV can enhance the vitality of HO-stimulated HaCaT cells, reduce intracellular ROS levels, and increase antioxidant enzyme activity in the cells. Further evaluation revealed that PTEV can inhibit UV-induced thickening of the epidermis and degradation of collagen fibers in mice by suppressing the overexpression of matrix metalloproteinase (MMP-3) induced by UV. It enhances the expression of type I collagen (COL1A1) and increases the activity of antioxidant enzymes, as well as the overall antioxidant capacity of tissues. Additionally, PTEV reduces the increase in malondialdehyde levels and lowers the expression levels of inflammatory factors TNF-α and IL-6, thereby protecting the skin barrier and function in mice with acute photodamage. Continuous production of PTEV offers promising applications in therapeutic strategies. |
| title | Utilizing Extracellular Vesicles from as a Novel Approach for Protecting the Skin from Oxidative Damage. |
| topic | Extracellular Vesicles Animals Oxidative Stress Humans Mice Ultraviolet Rays Skin Hydrogen Peroxide HaCaT Cells Diatoms Antioxidants Reactive Oxygen Species |
| url | https://pubmed.ncbi.nlm.nih.gov/40396567/ |