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通过pH调控量身定制用于自噬可视化的新型聚集诱导发光荧光探针的从头设计。

De novo design of a novel AIE fluorescent probe tailored to autophagy visualization via pH manipulation.

作者信息

Huang Xueyan, Chen Fei, Ma Yeshuo, Zheng Fan, Fang Yanpeng, Feng Bin, Huang Shuai, Zeng Hongliang, Zeng Wenbin

机构信息

Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.

Hunan Key Laboratory of Diagnostic and Therapeutic Drug Research for Chronic Diseases, Changsha, China.

出版信息

Biomater Res. 2023 Mar 13;27(1):20. doi: 10.1186/s40824-023-00359-w.

Abstract

BACKGROUND

Macroautophagy is an essential cellular self-protection mechanism, and defective autophagy has been considered to contribute to a variety of diseases. During the process, cytoplasmic components are transported via autophagosomes to acidic lysosomes for metabolism and recycling, which represents application niches for lysosome-targeted fluorescent probes. Additionally, in view of the complexity of the autophagy pathway, it entails more stringent requirements for probes suitable for monitoring autophagy. Meanwhile, aggregation-induced emission (AIE) fluorescent probes have been impressively demonstrated in the biomedical field, which bring fascinating possibilities to the autophagy visualization.

METHODS

We reported a generalizable de novo design of a novel pH-sensitive AIE probe ASMP-AP tailored to lysosome targeting for the interpretation of autophagy. Firstly, the theoretical calculation was carried out followed by the investigation of optical properties. Then, the performance of ASMP-AP in visualizing autophagy was corroborated by starvation or drugs treatments. Furthermore, the capability of ASMP-AP to monitor autophagy was demonstrated in ex vivo liver tissue and zebrafish in vivo.

RESULTS

ASMP-AP displays a large stokes shift, great cell permeability and good biocompatibility. More importantly, ASMP-AP enables a good linear response to pH, which derives from the fact that its aggregation state can be manipulated by the acidity. It was successfully applied for imaging autophagy in living cells and was proved capable of monitoring mitophagy. Moreover, this novel molecular tool was validated by ex vivo visualization of activated autophagy in drug-induced liver injury model. Interestingly, it provided a meaningful pharmacological insight that the melanin inhibitor 1-phenyl-2-thiourea (PTU)-induced autophagy was clearly presented in wild-type zebrafish.

CONCLUSIONS

ASMP-AP offers a simple yet effective tool for studying lysosome and autophagy. This is the first instance to visualize autophagy in zebrafish using a small-molecule probe with AIE characters, accurate lysosome targeting and simultaneous pH sensitivity. Ultimately, this novel fluorescent system has great potential for in vivo translation to fuel autophagy research.

摘要

背景

巨自噬是一种重要的细胞自我保护机制,自噬缺陷被认为与多种疾病有关。在此过程中,细胞质成分通过自噬体被运输到酸性溶酶体进行代谢和再循环,这为溶酶体靶向荧光探针提供了应用空间。此外,鉴于自噬途径的复杂性,对适用于监测自噬的探针有更严格的要求。同时,聚集诱导发光(AIE)荧光探针在生物医学领域已得到令人瞩目的证明,这为自噬可视化带来了迷人的可能性。

方法

我们报道了一种通用的从头设计的新型pH敏感AIE探针ASMP-AP,其专为溶酶体靶向而设计,用于解释自噬。首先进行理论计算,然后研究光学性质。然后,通过饥饿或药物处理证实了ASMP-AP在可视化自噬方面的性能。此外,在离体肝组织和斑马鱼体内证明了ASMP-AP监测自噬的能力。

结果

ASMP-AP表现出大的斯托克斯位移、良好的细胞通透性和良好的生物相容性。更重要的是,ASMP-AP对pH具有良好的线性响应,这源于其聚集状态可被酸度操纵这一事实。它成功应用于活细胞中的自噬成像,并被证明能够监测线粒体自噬。此外,这种新型分子工具在药物性肝损伤模型中通过离体可视化活化自噬得到了验证。有趣的是,它提供了一个有意义的药理学见解,即黑色素抑制剂1-苯基-2-硫脲(PTU)诱导的自噬在野生型斑马鱼中清晰可见。

结论

ASMP-AP为研究溶酶体和自噬提供了一种简单而有效的工具。这是首次使用具有AIE特性、精确溶酶体靶向和同时具有pH敏感性的小分子探针在斑马鱼中可视化自噬。最终,这种新型荧光系统在体内转化以推动自噬研究方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfa0/10012510/d718f9c1c12c/40824_2023_359_Sch1_HTML.jpg

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