微泡
角质形成细胞
银屑病
细胞因子
炎症
促炎细胞因子
免疫学
免疫系统
伊米奎莫德
医学
细胞生物学
生物
小RNA
体外
生物化学
基因
作者
Man Jiang,Hui Fang,Shuai Shao,Erle Dang,Jieyu Zhang,Pei Qiao,Angang Yang,Gang Wang
标识
DOI:10.1096/fj.201900642r
摘要
that cytokine-treated keratinocyte exosomes participated in the skin lesion development of imiquimod-induced psoriasis-like mouse model. Collectively, we reveal that the release of exosomes works as a way of keratinocyte-neutrophil communication, indicating that keratinocyte exosomes, with their specific cargoes, are therapeutic candidates for psoriasis.-Jiang, M., Fang, H., Shao, S., Dang, E., Zhang, J., Qiao, P., Yang, A., Wang, G. Keratinocyte exosomes activate neutrophils and enhance skin inflammation in psoriasis.
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