Evidence map›Paper›PMID 41880568›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Endogenous ATP-powered nanomotors directing neural stem cell differentiation for Parkinson's disease treatment.

Miaomiao Ding, Bin Chen, Jing Xiao, Jinghui Rong, Ye Feng, Chao Gao, Dailing Du, Yingfeng Tu, Fei Peng

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. 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
–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

1 citing paper in PubMed.

  1. Review
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.

Miaomiao Ding *School of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.ORCID 0009-0005-5832-4571
Bin Chen *School of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.ORCID 0009-0005-0828-0013
Jing XiaoSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Jinghui RongSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Ye FengSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Chao GaoSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Dailing DuSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.
Yingfeng TuNational Medical Products Administration Key Laboratory for Research and Evaluation of Drug Metabolism & Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.ORCID 0000-0003-2605-0172
Fei PengSchool of Materials Science and Engineering, Sun Yat-sen University, Guangzhou 510275, China.

Funding

MOST | National Key Research and Development Program of China (NKPs) 2022YFA1206900MOST | National Natural Science Foundation of China (NSFC) 22375224
6 · The paper itself

Abstract

Transplantation-free neuron regeneration remains attractive yet unsolved for reversing Parkinson's disease (PD). Here, we present enzyme-driven mesoporous gold nanomotors (Apyrase@Au) that leverage endogenous biochemical energy for spatiotemporally controlled promotion of neural stem cell (NSC) differentiation, without exogenous stem cell transplantation. By catalyzing endogenous adenosine triphosphate (ATP) hydrolysis, Apyrase@Au nanomotors simultaneously generate directional propulsion and localized signaling messenger protons. These protons induce calcium influx and activate quiescent NSCs within the ventricular-subventricular zone of PD mice, directing their differentiation into functional neurons and alleviating moving dysfunction. The bioenergy-converting system imparts dual functionality to active matter, propelling while concurrently yielding bioactive products. This work demonstrates the potential of ATP-powered nanomachines as a self-sustaining and targeted biointerface, offering a promising strategy for promoting NSC differentiation and alleviating moving dysfunction in degenerative diseases.

Indexed as

Adenosine TriphosphateCell DifferentiationNeural Stem CellsParkinson DiseaseAnimalsApyraseGoldMiceNeuronsAdenosine TriphosphateApyraseGoldapyraseendogenous ATPnanomotorsneural stem cell differentiationParkinson’s disease

Identifiers

PMID41880568
PMCPMC13037914

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.