光诱导枯草芽孢杆菌孢子转化用于肠道疾病治疗和疗效可视化

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY
Lin Kong, Wei He, Junyi Gong, Zijie Qiu, Zheng Zhao, Ben Zhong Tang
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引用次数: 0

摘要

将枯草芽孢杆菌无性细胞转化为孢子(BtS 转化)的有效策略仍然有限,尽管它们在治疗炎症性肠病(IBD)方面大有可为。现在介绍一种新颖、简单、快速的光诱导 BtS 转化机制,该机制利用一种新型聚集诱导发射发光剂(AIEgen)光敏剂,即三苯胺-苯并噻二唑-吡啶-对甲苯硼酸溴盐(TBPBB),在光照下会产生活性氧(ROS)。ROS 选择性地靶向破坏枯草芽孢杆菌的膜,并促使它们转化为芽孢。这些孢子在小鼠疾病模型中显示出有效治疗肠道疾病的巨大前景。此外,TBPBB 产生的荧光信号可用于直接观察受损肠道组织的恢复情况。这是监测愈合过程和深入了解疗效的重要工具。这项研究凸显了 AIEgen 诱导的 BtS 转化在识别、定位和可视化 IBD 治疗结果方面的显著实用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Photo-induced Bacillus subtilis-spore transformation for bowel disease therapy and therapeutic outcome visualization

Photo-induced Bacillus subtilis-spore transformation for bowel disease therapy and therapeutic outcome visualization

Photo-induced Bacillus subtilis-spore transformation for bowel disease therapy and therapeutic outcome visualization

Efficient strategies for transforming Bacillus subtilis vegetative cells into spores (BtS transformation) are still limited, although they show promise for the treatment of inflammatory bowel disease (IBD). A novel, simple, and rapid photo-induced BtS transformation mechanism is now presented that utilizes a novel aggregation-induced emission luminogen (AIEgen) photosensitizer, triphenylamine-benzothiadiazole-pyridine-p-tolylboronic acid bromine salt (TBPBB), that generates reactive oxygen species (ROS) when exposed to light. The ROS selectively target and damage the membranes of Bacillus subtilis and trigger their transformation into spores. These spores demonstrate considerable promise for the effective treatment of IBD in a mouse disease model. Furthermore, the fluorescence signal generated by TBPBB can be used to directly visualize the recovery of damaged intestinal tissue. This is a valuable tool for monitoring the healing process and gaining insights into therapeutic efficacy. This study highlights the remarkable practical value of AIEgen-induced BtS transformation for identifying, localizing, and visualizing the therapeutic outcomes of IBD treatments.

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来源期刊
CiteScore
17.40
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