Evidence map›Paper›PMID 39721010›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Functional Monomers Equipped Microgel System for Managing Parkinson's Disease by Intervening Chemokine Axis-mediated Nerve Cell Communications.

Lin Jiang, Xu Zhang, Shun Wang, Jiangkuan Zhang, Junyang Chen, Jiachuan Lu, Liting Yao, Weiwei Jin, Nan Li, Qing Li

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

10 authors.

Lin JiangCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Xu ZhangDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.
Shun WangDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.
Jiangkuan ZhangDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.
Junyang ChenSchool of Life Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Jiachuan LuDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.
Liting YaoCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Weiwei JinCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Nan LiDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.
Qing LiDepartment of Neurology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou University, Zhengzhou, 450052, China.ORCID https://orcid.org/0000-0002-5290-1172

Funding

Joint Project of Medical Science and Technology of Henan Province LHGJ20220458Joint Project of Medical Science and Technology of Henan Province LHGJ20220459Joint Project of Medical Science and Technology of Henan Province LHGJ20230348Young and Middle-Aged Health Science and Technology Innovation Leading Talent Training Program of Henan Province LJRC2023005
6 · The paper itself

Abstract

The complex pathology of Parkinson's disease (PD) requires comprehensive understanding and multi-pronged interventions for communication between nerve cells. Despite new developments in nanotechnology in the treatment of PD, in-depth exploration of their biological effects, in particular, the specific mechanisms of inflammation inhibition are lacking. Herein, using the stable cascade catalysis channel formed by polydopamine (PDA), imidazole groups, and Cu ions, a microgel system comprising functional monomers [superoxide dismutase (SOD) with double bonds, PDA, 2-methacryloyloxy ethyl phosphorylcholine (MPC), and Cu ions] is proposed for managing PD. The microgel can be efficiently delivered to the brain aided by MPC, after which a multi-level regulatory strategy targeting neurons and microglia can be initiated. The catalytic activity cascade elicited by SOD and Cu ions can regulate the anti-inflammatory phenotypic transformation of microglia by relieving oxidative stress. Meanwhile, the dopamine (DA) released from PDA can facilitate DA storage and neurogenesis, inhibiting CX3CL1 release and the CX3CR1 receptor on microglia and further regulating the CX3CL1/CX3CR1-NF-κB-NLRP3 signaling pathway in microglia to inhibit neuroinflammation. Therefore, the proposed microgel delivery system with functional monomers represents a promising therapeutic strategy for managing neuroinflammation and promoting neurogenesis in PD by intervening chemokine axis-mediated communication between neurons and microglia.

Indexed as

Cell CommunicationChemokinesNeuronsParkinson DiseaseAnimalsCopperDopamineDrug Delivery SystemsGelsHumansIndolesMiceMicrogliaPhosphorylcholinePolymersSuperoxide DismutaseChemokinesCopperDopamineGelsIndolesPhosphorylcholinepolydopaminePolymersSuperoxide Dismutasechemokine axisfunctional monomersmicrogel systemsneuroinflammationsParkinson's diseases

Identifiers

PMID39721010
PMCPMC11831437

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Registered trials

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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.