Evidence map›Paper›PMID 39617787›Full record

ArticleExperimental & molecular medicine2024

Astrocyte-neuron crosstalk through extracellular vesicle-shuttled miRNA-382-5p promotes traumatic brain injury.

Qing Hu, Xun Wu, Chengxuan Guo, Tinghao Wang, Hao Guo, Jin Wang, Bodong Wang, Wenxing Cui, Hao Bai, Jinpeng Zhou and 11 more

Abstract read
In one paragraph

Article in Experimental & molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Research progress on biomarkers of traumatic brain injury.Animal models and experimental medicine · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Extracellular RNAs as Messengers and Early Biomarkers in Neurodegeneration.International journal of molecular sciences · 2025
    Review
  11. Review
  12. 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

21 authors.

Qing Hu *Department of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Xun Wu *Department of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Chengxuan Guo *Department of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Tinghao WangDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Hao GuoDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Jin WangDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Bodong WangDepartment of Neurosurgery, The 960th Hospital of the PLA Joint Logistics Support Force, Jinan, Shandong, China.
Wenxing CuiDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Hao BaiDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Jinpeng ZhouDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Leiyang LiDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Liying HanDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Liang CaoDepartment of Traditional Chinese Medicine, Tangdu Hospital, Xi'an, Shaanxi, China.
Shunnan GeDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.ORCID 0000-0003-1338-830X
Guodong GaoDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Ting WangState Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai, China.
Zhenyong WuUniversity of Chinese Academy of Sciences, Beijing, China.
Wei GuoDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China.
Yan QuDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China. yanqu0123@fmmu.edu.cn.ORCID 0000-0001-5434-7390
Jing FengState Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Science, Shanghai, China. fengjing@simm.ac.cn.ORCID 0000-0001-6726-7912
Haixiao LiuDepartment of Neurosurgery, Tangdu Hospital, Xi'an, Shaanxi, China. lhxiao@fmmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although astrocytes undergo functional changes in response to brain injury and may be the driving force of subsequent neuronal death, the underlying mechanisms remain incompletely elucidated. Here, we showed that extracellular vesicle (EV)-shuttled miRNA-382-5p may serve as a biomarker for the severity of traumatic brain injury (TBI), as the circulating EV-miRNA-382-5p level was significantly increased in both human patients and TBI model mice. Mechanistically, astrocyte-derived EVs delivered the shuttled miRNA-382-5p to mediate astrocyte-neuron communication, which promoted neuronal mitochondrial dysfunction by inhibiting the expression of optic atrophy-1 (OPA1). Consistent with these findings, genetic ablation of neuronal OPA1 exacerbated mitochondrial damage and neuronal apoptosis in response to TBI. Moreover, engineered RVG-miRNA-382-5p inhibitor-EVs, which can selectively deliver a miRNA-382-5p inhibitor to neurons, significantly attenuated mitochondrial damage and improved neurological function after TBI. Taken together, our data suggest that EV-shuttled miRNA-382-5p may be a critical mediator of astrocyte-induced neurotoxicity under pathological conditions and that targeting miRNA-382-5p-OPA1 signaling has potential for clinical translation in the treatment of traumatic brain injury.

Indexed as

AstrocytesBrain Injuries, TraumaticExtracellular VesiclesMicroRNAsNeuronsAnimalsApoptosisCell CommunicationDisease Models, AnimalHumansMaleMiceMitochondriaMicroRNAs

Identifiers

PMID39617787
PMCPMC11671591

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.