Evidence map›Paper›PMID 39578796›Full record

ArticleJournal of nanobiotechnology2024

ROS-responsive nanoparticles for bioimaging and treating acute lung injury by releasing dexamethasone and improving alveolar macrophage homeostasis.

Wenna Fan, Yongyao Tang, Yamin Liu, Ya Ran, Guangrui Pan, Xin Song, Li Mai, Xue Jiang, Dan Chen, Fangzhou Song and 1 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

11 authors.

Wenna Fan *Institute of Intelligent Chinese Medicine, Chongqing University of Chinese Medicine, Chongqing, 402760, China.
Yongyao Tang *Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China.
Yamin Liu *Department of Obstetrics and Gyecology, Women and Children's Hospital of Chongqing Medical University/Chongqing Health Center for Women and Children, Chongqing, 400016, China.
Ya Ran *Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China.
Guangrui Pan *General Surgery (Breast Surgery), The Affiliated Hospital of Southwest Medical University, 25 Taiping Rd, Jiangyang District, Luzhou, 646000, Sichuan, China.
Xin Song *Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China.
Li MaiDepartment of Laboratory Medicine, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
Xue JiangMolecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China.
Dan ChenMolecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China.
Fangzhou SongMolecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, 400016, China. fzsong@cqmu.edu.cn.
Haiyu LiInstitute of Intelligent Chinese Medicine, Chongqing University of Chinese Medicine, Chongqing, 402760, China. lihaiyu@cqmu.edu.cn.

Funding

National Natural Science Foundation of China [No.82002154]
6 · The paper itself

Abstract

backgroundAcute lung injury (ALI) triggers the activation of pulmonary macrophages, which in turn produce excessive amounts of reactive oxygen species (ROS).

resultsWe synthesized ROS-responsive red light-emitting carbon dots (RCMNs) that target lung macrophages, possess bioimaging capabilities, and efficiently eliminate intracellular ROS, thereby demonstrating anti-inflammatory effects for treating acute lung injury (ALI). In an LPS-induced ALI mouse model, RCMNs showed bioimaging and therapeutic potential, reducing lung damage and inflammation by targeting ROS-damaged tissue. RCMNs also improved alveolar macrophage activity, decreased inflammatory cytokines (TNF-α and IL-6), and enhanced survival in endotoxic shock, indicating their therapeutic potential for ALI. RNA-seq analysis revealed that RCMNs modulate signaling pathways related to calcium, TNF, and Toll-like receptors, highlighting their role in regulating inflammation and immune responses. Mechanistically, RCMNs alleviate inflammation in ALI by enhancing mitochondrial function in lung macrophages, as evidenced by improved mitochondrial morphology and membrane potential.

conclusionsThis protective effect is mediated through the regulation of intracellular Ca

Indexed as

Acute Lung InjuryDexamethasoneHomeostasisMacrophages, AlveolarNanoparticlesReactive Oxygen SpeciesAnimalsAnti-Inflammatory AgentsCytokinesInflammationLipopolysaccharidesMaleMiceMice, Inbred C57BLMitochondriaQuantum DotsAnti-Inflammatory AgentsCytokinesDexamethasoneLipopolysaccharidesReactive Oxygen SpeciesAcute lung injuryAlveolar macrophagesMitochondrial functionRCMNs nanoparticle

Identifiers

PMID39578796
PMCPMC11585220

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.