Evidence map›Paper›PMID 36314052›Full record

ArticleBrain : a journal of neurology2023

Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.

Lara El-Bazzal, Adeline Ghata, Clothilde Estève, Jihane Gadacha, Patrice Quintana, Christel Castro, Nathalie Roeckel-Trévisiol, Frédérique Lembo, Nicolas Lenfant, André Mégarbané and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Junctions in Jeopardy: the neuromuscular junction is a selective pathological target in Charcot-Marie-Tooth disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Effects of intensive rehabilitation on functioning in patients with mild and moderate Charcot-Marie-Tooth disease: a real-practice retrospective study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    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

17 authors at 4 institutions in 3 countries.

Lara El-BazzalAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Adeline GhataAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Clothilde EstèveAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Jihane GadachaAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Patrice QuintanaAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Christel CastroAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Nathalie Roeckel-TrévisiolAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Frédérique LemboAix Marseille Univ, INSERM, CNRS, CRCM, Institut Paoli-Calmettes, Marseille, France.
Nicolas LenfantAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
André MégarbanéDepartment of Human Genetics, Gilbert and Rose-Marie Chagoury School of Medicine, Lebanese American University, Beirut, Lebanon.
Jean-Paul BorgAix Marseille Univ, INSERM, CNRS, CRCM, Institut Paoli-Calmettes, Marseille, France.
Nicolas LévyAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Marc BartoliAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.ORCID 0000-0003-3339-9858
Yannick PoitelonDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA.ORCID 0000-0001-9868-1569
Pierre L RoubertouxAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.
Valérie DelagueAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.ORCID 0000-0003-2652-362X
Nathalie Bernard-MarissalAix Marseille Univ, INSERM, MMG, U 1251, Marseille, France.ORCID 0000-0002-2160-2612
Inserm · FRCentre National de la Recherche Scientifique · FRAlbany Medical Center Hospital · USLebanese American University · LB

Funding

Transduction of Mechanical Stimuli in Myelination and Peripheral Nerve RepairR01NS110627 · NINDS · ALBANY MEDICAL COLLEGE · PI POITELON, YANNICK · 2020 to 2024
$2.1M
NINDS NIH HHS R01 NS110627
6 · The paper itself

Abstract

Charcot-Marie-Tooth (CMT) disease is one of the most common inherited neurological disorders, affecting either axons from the motor and/or sensory neurons or Schwann cells of the peripheral nervous system (PNS) and caused by more than 100 genes. We previously identified mutations in FGD4 as responsible for CMT4H, an autosomal recessive demyelinating form of CMT disease. FGD4 encodes FRABIN, a GDP/GTP nucleotide exchange factor, particularly for the small GTPase Cdc42. Remarkably, nerves from patients with CMT4H display excessive redundant myelin figures called outfoldings that arise from focal hypermyelination, suggesting that FRABIN could play a role in the control of PNS myelination. To gain insights into the role of FGD4/FRABIN in Schwann cell myelination, we generated a knockout mouse model (Fgd4SC-/-), with conditional ablation of Fgd4 in Schwann cells. We show that the specific deletion of FRABIN in Schwann cells leads to aberrant myelination in vitro, in dorsal root ganglia neuron/Schwann cell co-cultures, as well as in vivo, in distal sciatic nerves from Fgd4SC-/- mice. We observed that those myelination defects are related to an upregulation of some interactors of the NRG1 type III/ERBB2/3 signalling pathway, which is known to ensure a proper level of myelination in the PNS. Based on a yeast two-hybrid screen, we identified SNX3 as a new partner of FRABIN, which is involved in the regulation of endocytic trafficking. Interestingly, we showed that the loss of FRABIN impairs endocytic trafficking, which may contribute to the defective NRG1 type III/ERBB2/3 signalling and myelination. Using RNA-Seq, in vitro, we identified new potential effectors of the deregulated pathways, such as ERBIN, RAB11FIP2 and MAF, thereby providing cues to understand how FRABIN contributes to proper ERBB2 trafficking or even myelin membrane addition through cholesterol synthesis. Finally, we showed that the re-establishment of proper levels of the NRG1 type III/ERBB2/3 pathway using niacin treatment reduces myelin outfoldings in nerves of CMT4H mice. Overall, our work reveals a new role of FRABIN in the regulation of NRG1 type III/ERBB2/3 NRG1signalling and myelination and opens future therapeutic strategies based on the modulation of the NRG1 type III/ERBB2/3 pathway to reduce CMT4H pathology and more generally other demyelinating types of CMT disease.

Indexed as

Charcot-Marie-Tooth DiseaseAnimalsErb-b2 Receptor Tyrosine KinasesGuanine Nucleotide Exchange FactorsMiceMice, KnockoutMutationNeuregulin-1Receptor, ErbB-3Schwann CellsSciatic NerveSorting NexinsErbb2 protein, mouseErb-b2 Receptor Tyrosine KinasesErbB3 protein, mouseGuanine Nucleotide Exchange FactorsNeuregulin-1Nrg1 protein, mouseReceptor, ErbB-3Snx3 protein, mouseSorting NexinsCharcot–Marie–Toothendocytic traffickingmyelin outfoldingsniacin treatmentNRG1/ERBB2/3

Identifiers

PMID36314052
PMCPMC10151191
OpenAlexW4307774269

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.