Evidence map›Paper›PMID 40660236›Full record

ArticleJournal of nanobiotechnology2025

Engineered Panax notoginseng polysaccharide micelles inhibit macrophage polarization and delay the progression of rheumatoid arthritis via JAK2-STAT3 signaling pathway.

Yang Yu, Liang Kong, Rui-Bo Guo, Ya-Ni Zhang, Shu-Tong Li, Feng-Yuan Zhang, Xin Wang, Yang Liu, Xiu-Ying Li, Xue-Tao Li

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Microglia-targetedMaterials today. Bio · 2026
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  9. ESCRT-Mimetic Nanodegrader Targets STING for Anti-Inflammatory Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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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.

Yang Yu *College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Liang Kong *College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Rui-Bo Guo *College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Ya-Ni ZhangCollege of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Shu-Tong LiCollege of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Feng-Yuan ZhangShanxi Key Laboratory of Innovative Drug for the Treatment of Serious Diseases Basing on the Chronic Inflammation, Shanxi University of Chinese Medicine, Jinzhong, 030619, China.
Xin WangShanxi Key Laboratory of Innovative Drug for the Treatment of Serious Diseases Basing on the Chronic Inflammation, Shanxi University of Chinese Medicine, Jinzhong, 030619, China.
Yang LiuCollege of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China.
Xiu-Ying LiShanxi Key Laboratory of Innovative Drug for the Treatment of Serious Diseases Basing on the Chronic Inflammation, Shanxi University of Chinese Medicine, Jinzhong, 030619, China. lixiuying85@163.com.
Xue-Tao LiCollege of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, 116600, China. lixuetao1979@163.com.

Funding

Excellent Graduate Program of Liaoning Provincial Department of Education 2024-JYTCB-048National Natural Science Foundation of China 82204629Youth Innovation Team Project of Liaoning Provincial Department of Education 2024-JYTCB-077Youth Innovation Team Project of Liaoning Provincial Department of Education 2024-JYTCB-085
6 · The paper itself

Abstract

backgroundThe imbalance of macrophage polarization plays a pivotal role in the progression of rheumatoid arthritis (RA). Reprogramming macrophages from the pro-inflammatory M1 phenotype to the anti-inflammatory M2 phenotype is considered a promising therapeutic strategy.

methodsTo address this challenge, Panax notoginseng polysaccharides (PNP) with varying molecular weights were chemically conjugated with deoxycholic acid (DC) to obtain amphiphilic conjugates (PNP-DC), which self-assembled into micelles (PNP-Ms). After screening for optimal molecular weight, folic acid (FA) was introduced onto the micelle surface, and Polyphyllin I (PPI) was encapsulated to form FA-modified, PPI-loaded micelles (FA-PPI-Ms) with macrophage-targeting capability.

resultsFA-PPI-Ms showed enhanced cellular uptake via FA receptor-mediated endocytosis and effectively eliminated reactive oxygen species (ROS), reduced inflammatory cytokine production, and exhibited good biosafety. In vivo, FA-PPI-Ms significantly alleviated joint swelling and inflammation in RA rat models. Mechanistic studies based on RNA sequencing and experimental validation revealed that FA-PPI-Ms suppressed the JAK2/STAT3 signaling pathway, thereby promoting M2 macrophage polarization and restoring the M1/M2 balance.

conclusionThis study presents a novel FA-PPI-Ms delivery system for targeted macrophages. By modulating polarization through inhibition of JAK2/STAT3 signaling, the system offers a promising therapeutic strategy for RA and potentially other inflammatory diseases.

Indexed as

Arthritis, RheumatoidJanus Kinase 2MacrophagesPanax notoginsengPolysaccharidesSTAT3 Transcription FactorAnimalsHumansMaleMiceMicellesRatsRats, Sprague-DawleyRAW 264.7 CellsReactive Oxygen SpeciesSignal TransductionJanus Kinase 2MicellesPolysaccharidesReactive Oxygen SpeciesSTAT3 Transcription FactorJAK2-STAT3Macrophage polarizationMicellesPanax Notoginseng polysaccharideRheumatoid arthritis

Identifiers

PMID40660236
PMCPMC12261558

What OpenQuestion holds

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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.