Evidence map›Paper›PMID 39513915›Full record

ArticleCells2024

Sonic Hedgehog Is an Early Oligodendrocyte Marker During Remyelination.

Mariagiovanna Russo, Amina Zahaf, Abdelmoumen Kassoussi, Ariane Sharif, Hélène Faure, Elisabeth Traiffort, Martial Ruat

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Mariagiovanna RussoParis-Saclay University, CNRS, Neuroscience Paris-Saclay Institute, 91400 Saclay, France.
Amina ZahafParis-Saclay University, INSERM, Diseases and Hormones of the Nervous System-U1195, 94276 Le Kremlin-Bicêtre, France.ORCID 0000-0002-4974-7020
Abdelmoumen KassoussiParis-Saclay University, CNRS, Neuroscience Paris-Saclay Institute, 91400 Saclay, France.ORCID 0000-0002-7082-4764
Ariane SharifLaboratory of Development and Plasticity of the Neuroendocrine Brain, Lille Neuroscience & Cognition, UMR-S 1172, FHU 1000 Days for Health, INSERM, Université de Lille, CHU Lille, 59000 Lille, France.ORCID 0000-0003-0810-400X
Hélène FaureParis-Saclay University, CNRS, Neuroscience Paris-Saclay Institute, 91400 Saclay, France.ORCID 0000-0002-0005-9331
Elisabeth TraiffortParis-Saclay University, INSERM, Diseases and Hormones of the Nervous System-U1195, 94276 Le Kremlin-Bicêtre, France.ORCID 0000-0002-9645-6269
Martial RuatParis-Saclay University, CNRS, Neuroscience Paris-Saclay Institute, 91400 Saclay, France.

Funding

Fondation d'Aide pour la Recherche sur la Sclerose en Plaques RAK21128LLAFondation pour la Recherche Médicale FDT202106013169France Sclérose en Plaques Fance SEP-27Université Paris-Sud 2018-192
6 · The paper itself

Abstract

Failure of myelin regeneration by oligodendrocytes contributes to progressive decline in many neurological diseases. Here, using in vitro and in vivo rodent models, functional blockade, and mouse brain demyelination, we demonstrate that Sonic hedgehog (Shh) expression in a subset of oligodendrocyte progenitor cells precedes the expression of myelin basic protein (MBP), a major myelin sheath protein. Primary cultures of rodent cortical oligodendrocytes show that Shh mRNA and protein are upregulated during oligodendrocyte maturation before the upregulation of MBP expression. Importantly, almost all MBP-positive cells are Shh positive during differentiation. During remyelination, we identify a rapid induction of Shh mRNA and peptide in oligodendroglial cells present in the demyelinated corpus callosum of mice, including a population of PDGFRα-expressing cells. Shh invalidation by an adeno-associated virus strategy demonstrates that the downregulation of Shh impairs the differentiation of oligodendrocytes in vitro and decreases MBP and myelin proteolipid protein expression in the demyelinated mouse brain at late stages of remyelination. We also report a parallel expression of Shh and MBP in oligodendroglial cells during early post-natal myelination of the mouse brain. Thus, we identify a crucial Shh signal involved in oligodendroglial cell differentiation and remyelination, with potential interest in the design of better-targeted remyelinating therapeutic strategies.

Indexed as

Cell DifferentiationHedgehog ProteinsOligodendrogliaRemyelinationAnimalsBiomarkersCells, CulturedCorpus CallosumDemyelinating DiseasesMiceMice, Inbred C57BLMyelin Basic ProteinMyelin SheathBiomarkersHedgehog ProteinsMyelin Basic ProteinShh protein, mouseAAV vectorsdemyelinating diseasehedgehog signalingplatelet-derived growth factor receptor alphapost-natal brain

Identifiers

PMID39513915
PMCPMC11545011

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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.