Evidence map›Paper›PMID 39119832›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Irisin-Encapsulated Mitochondria-Targeted Biomimetic Nanotherapeutics for Alleviating Acute Kidney Injury.

Xia Zhang, Lijia Liang, Fengxian Wang, Pedro A Jose, Ken Chen, Chunyu Zeng

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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.

  1. Review
  2. Biomimetic materials for medical applications.Chinese medical journal · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Autophagy · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

6 authors.

Xia ZhangDepartment of Cardiology, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, P. R. China.
Lijia LiangKey Laboratory of Geriatric Cardiovascular and Cerebrovascular Disease Research, Ministry of Education of China, Chongqing, 400042, P. R. China.ORCID 0000-0002-9774-0667
Fengxian WangDepartment of Cardiology, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, P. R. China.
Pedro A JoseDivision of Renal Diseases & Hypertension, Department of Medicine and Pharmacology-Physiology, The George Washington University School of Medicine & Health Sciences, Washington DC, 20037, USA.
Ken ChenDepartment of Cardiology, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, P. R. China.
Chunyu ZengDepartment of Cardiology, Daping Hospital, Third Military Medical University (Army Medical University), Chongqing, 400042, P. R. China.ORCID 0009-0009-5059-2159

Funding

Chongqing Science and Technology Bureau cstc2020jcyj-msxmX1051National Key R&D Program of China 2022YFA1104500National Natural Science Foundation of China 81930008National Natural Science Foundation of China 82100318
6 · The paper itself

Abstract

Acute kidney injury (AKI) is the sudden decrease in renal function that can be attributed to dysregulated reactive oxygen species (ROS) production and impaired mitochondrial function. Irisin, a type I membrane protein secreted by skeletal muscles in response to physical activity, has been reported to alleviate kidney damage through regulation of mitochondrial biogenesis and oxidative metabolism. In this study, a macrophage membrane-coated metal-organic framework (MCM@MOF) is developed as a nanocarrier for encapsulating irisin to overcome the inherent characteristics of irisin, including a short circulation time, limited kidney-targeting ability, and low membrane permeability. The engineered irisin-mediated biomimetic nanotherapeutics have extended circulation time and enhanced targeting capability toward injured kidneys due to the preservation of macrophage membrane proteins. The irisin-encapsulated biomimetic nanotherapeutics effectively mitigate acute ischemia-reperfusion injury by protecting mitochondrial function and modulating SOD2 levels in renal tubular epithelial cells. The present study provides novel insights to advance the development of irisin as a potential therapeutic approach for AKI.

Indexed as

Acute Kidney InjuryDisease Models, AnimalFibronectinsMitochondriaAnimalsBiomimetic MaterialsBiomimeticsHumansMaleMetal-Organic FrameworksMiceNanoparticlesReactive Oxygen SpeciesFibronectinsMetal-Organic FrameworksReactive Oxygen Speciesacute kidney injurybiomimetic nanocarriersirisinmitochondria

Identifiers

PMID39119832
PMCPMC11481180

What OpenQuestion holds

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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.