Evidence map›Paper›PMID 36915215›Full record

ArticleBiomaterials research2023

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

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

Open access · goldFull text read
In one paragraph

Article in Biomaterials research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Xueyan Huang *Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Fei Chen *Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Yeshuo MaDepartment of Geriatrics, Third Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Fan ZhengXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Yanpeng FangXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Bin FengXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Shuai HuangXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China.
Hongliang ZengHunan Academic of Chinese Medicine, Inst Chinese Mat Med, Changsha, People's Republic of China. zenghl155@163.com.
Wenbin ZengXiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, People's Republic of China. wbzeng@hotmail.com.
Central South University · CN

Funding

National Natural Science Foundation of China 22107123National Natural Science Foundation of China 81974386National Natural Science Foundation of China 82272067National Natural Science Foundation of China M-0696
6 · The paper itself

Abstract

backgroundMacroautophagy 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.

methodsWe 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.

resultsASMP-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.

conclusionsASMP-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.

Indexed as

AIE fluorescent probeAutophagy visualizationBiomaterials imagingLysosome-targeting

Identifiers

PMID36915215
PMCPMC10012510
OpenAlexW4324046735

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read37
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.