Evidence map›Paper›PMID 38015636›Full record

ArticleThe Journal of clinical investigation2024

Histone methyltransferase Ezh2 coordinates mammalian axon regeneration via regulation of key regenerative pathways.

Xue-Wei Wang, Shu-Guang Yang, Ming-Wen Hu, Rui-Ying Wang, Chi Zhang, Anish R Kosanam, Arinze J Ochuba, Jing-Jing Jiang, Ximei Luo, Yun Guan and 3 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. MiR-26a-5p/EZH2 Mediates Wnt2 Promoter Methylation to Regulate Trophoblast Dysfunction.Combinatorial chemistry & high throughput screening · 2026
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. The Role of Methylation Modification in Neural Injury and Repair.International journal of molecular sciences · 2025
    Review
  13. Review
  14. Review
  15. Roles of Kdm6a and Kdm6b in Regulation of Mammalian Neural Regeneration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

13 authors at 2 institutions in 2 countries.

Xue-Wei WangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Shu-Guang YangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Ming-Wen HuDepartment of Ophthalmology and.
Rui-Ying WangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Chi ZhangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Anish R KosanamDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Arinze J OchubaDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jing-Jing JiangDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Ximei LuoDepartment of Ophthalmology and.
Yun GuanDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jiang QianDepartment of Ophthalmology and.
Chang-Mei LiuState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Feng-Quan ZhouDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USChinese Academy of Sciences · CN

Funding

Murine Mutagenesis CoreP30NS050274 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KOLODKIN, ALEX L · 2005 to 2020
$10.9M
Reprogramming retinal ganglion cells for optic nerve regeneration and guidanceR01EY027347 · NEI · JOHNS HOPKINS UNIVERSITY · PI CAO, XU · 2017 to 2021
$2.0M
Targeting aging genes and pathways to promote optic nerve regenerationR01EY030883 · NEI · JOHNS HOPKINS UNIVERSITY · PI WAN, MEI · 2020 to 2024
$2.0M
Epigenetic regulation of neuronal morphogenesis in development and regenerationR01NS085176 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ZHOU, FENGQUAN · 2014 to 2018
$1.8M
Remodeling of chromatin and transcriptomic landscape to enhance optic nerve regenerationR01EY031779 · NEI · JOHNS HOPKINS UNIVERSITY · PI QIAN, JIANG · 2020 to 2023
$1.7M
Computational Tools for Single Cell Analysis: Application to Retinal DegenerationR01EY029548 · NEI · JOHNS HOPKINS UNIVERSITY · PI QIAN, JIANG, ZACK, DONALD J. · 2018 to 2021
$1.6M
Deciphering the Transcriptional Regulatory Network Controlling RGC Axon Growth to Promote RGC Axon Regeneration and Cell Survival after Axonal InjuryR00EY031742 · NEI · UNIVERSITY OF SOUTH FLORIDA · PI Xuewei Wang · 2024 to 2026
$747k
Deciphering the Transcriptional Regulatory Network Controlling RGC Axon Growth to Promote RGC Axon Regeneration and Cell Survival after Axonal InjuryK99EY031742 · NEI · JOHNS HOPKINS UNIVERSITY · PI WANG, XUEWEI · 2020 to 2023
$326k
NEI NIH HHS K99 EY031742NEI NIH HHS R00 EY031742NEI NIH HHS R01 EY027347NEI NIH HHS R01 EY029548NEI NIH HHS R01 EY030883NEI NIH HHS R01 EY031779NINDS NIH HHS P30 NS050274NINDS NIH HHS R01 NS085176
6 · The paper itself

Abstract

Current treatments for neurodegenerative diseases and neural injuries face major challenges, primarily due to the diminished regenerative capacity of neurons in the mammalian CNS as they mature. Here, we investigated the role of Ezh2, a histone methyltransferase, in regulating mammalian axon regeneration. We found that Ezh2 declined in the mouse nervous system during maturation but was upregulated in adult dorsal root ganglion neurons following peripheral nerve injury to facilitate spontaneous axon regeneration. In addition, overexpression of Ezh2 in retinal ganglion cells in the CNS promoted optic nerve regeneration via both histone methylation-dependent and -independent mechanisms. Further investigation revealed that Ezh2 fostered axon regeneration by orchestrating the transcriptional silencing of genes governing synaptic function and those inhibiting axon regeneration, while concurrently activating various factors that support axon regeneration. Notably, we demonstrated that GABA transporter 2, encoded by Slc6a13, acted downstream of Ezh2 to control axon regeneration. Overall, our study underscores the potential of modulating chromatin accessibility as a promising strategy for promoting CNS axon regeneration.

Indexed as

AxonsOptic Nerve InjuriesAnimalsEnhancer of Zeste Homolog 2 ProteinGanglia, SpinalMammalsMiceNerve RegenerationRetinal Ganglion CellsEnhancer of Zeste Homolog 2 ProteinEzh2 protein, mouseEpigeneticsNeurodegenerationNeurodevelopmentNeuroscienceOphthalmology

Identifiers

PMID38015636
PMCPMC10849760
OpenAlexW4389099954

What OpenQuestion holds

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LicenceCC BY
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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.