Photocatalytic Polyamine Depletion for the Treatment of Psoriasis AITranslate
Abstract AITranslate
Psoriasis is an incurable autoinflammatory disorder associated with metabolic abnormalities. Excessive polyamine production in keratinocytes plays a vital role in the initiation and progression of psoriasis. In this study, we propose a new strategy to degrade polyamines and ameliorate psoriasis development based on the new type of polyoxometalate (POMs)-based silver material C32H100Ag6O98P2S16W24 (HT-1). HT-1 possessed efficient peroxidase (POD) and oxidase (OXD)-like activities for promoting reactive oxygen species (ROS) generation under visible light (VIS) irradiation. The generated ROS from HT-1 efficiently decreased the levels of polyamines and reduced IL-17A-induced psoriatic responses in keratinocytes. Meanwhile, photocatalytic depletion of polyamines by HT-1 also reduced the endosomal self-RNA sensing in DCs, impairing the maturation and T cells priming function of DC, thereby attenuating the development of psoriasis. In summary, this study may pave the way for a promising treatment approach for psoriasis, even for other autoinflammatory diseases.
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DOI:https://doi.org/10.1021/acsmaterialslett.3c01140
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Psoriasis is an incurable autoinflammatory disorder associated with metabolic abnormalities. Excessive polyamine production in keratinocytes plays a vital role in the initiation and progression of psoriasis. In this study, we propose a new strategy to degrade polyamines and ameliorate psoriasis development based on the new type of polyoxometalate (POMs)-based silver material C32H100Ag6O98P2S16W24 (HT-1). HT-1 possessed efficient peroxidase (POD) and oxidase (OXD)-like activities for promoting reactive oxygen species (ROS) generation under visible light (VIS) irradiation. The generated ROS from HT-1 efficiently decreased the levels of polyamines and reduced IL-17A-induced psoriatic responses in keratinocytes. Meanwhile, photocatalytic depletion of polyamines by HT-1 also reduced the endosomal self-RNA sensing in DCs, impairing the maturation and T cells priming function of DC, thereby attenuating the development of psoriasis. In summary, this study may pave the way for a promising treatment approach for psoriasis, even for other autoinflammatory diseases.
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| GB/T 7714-2015 | [1] Ting Hu, Hui Yuan, Qianfeng He, et al. ACS Materials Letters, 2024(6). DOI:10.1021/acsmaterialslett.3c01140. |
| MLA | [1] Ting Hu, et al., ACS Materials Letters, no. 6, 2024, https://doi.org/10.1021/acsmaterialslett.3c01140. |
| APA | [1] Ting Hu, Hui Yuan, Qianfeng He, Jie Ren, Yan Qiu, Jianqing Lin, Yuhang Li, & Canzhong Lu. (2024). ACS Materials Letters(6). https://doi.org/10.1021/acsmaterialslett.3c01140 |
| IEEE | [1] Ting Hu, Hui Yuan, Qianfeng He, Jie Ren, Yan Qiu, Jianqing Lin, Yuhang Li, and Canzhong Lu, ACS Materials Letters, no. 6, 2024, doi: 10.1021/acsmaterialslett.3c01140. |
