Evidence map›Paper›PMID 35551393›Full record

ArticleHuman molecular genetics2022

Motor unit recovery following Smn restoration in mouse models of spinal muscular atrophy.

Laura H Comley, Rachel A Kline, Alison K Thomson, Victoria Woschitz, Eric Villalón Landeros, Erkan Y Osman, Christian L Lorson, Lyndsay M Murray

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. The neuropathy-causingbioRxiv : the preprint server for biology · 2026
    Article
  2. 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
  3. Review
  4. Article
  5. Review
  6. Article
  7. Journal of clinical medicine · 2024
    Article
  8. Article
  9. Postsynaptic receptors regulate presynaptic transmitter stability through transsynaptic bridges.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. 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

8 authors at 3 institutions in 2 countries.

Laura H ComleyCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Rachel A KlineCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Alison K ThomsonCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Victoria WoschitzCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Eric Villalón LanderosBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Erkan Y OsmanBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Christian L LorsonBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Lyndsay M MurrayCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, EH8 9XD, UK.ORCID 0000-0001-6841-702X
University of Edinburgh · GBMissouri College · USJohns Hopkins University · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is a childhood motor neuron disease caused by anomalies in the SMN1 gene. Although therapeutics have been approved for the treatment of SMA, there is a therapeutic time window, after which efficacy is reduced. Hallmarks of motor unit pathology in SMA include loss of motor-neurons and neuromuscular junction (NMJs). Following an increase in Smn levels, it is unclear how much damage can be repaired and the degree to which normal connections are re-established. Here, we perform a detailed analysis of motor unit pathology before and after restoration of Smn levels. Using a Smn-inducible mouse model of SMA, we show that genetic restoration of Smn results in a dramatic reduction in NMJ pathology, with restoration of innervation patterns, preservation of axon and endplate number and normalized expression of P53-associated transcripts. Notably, presynaptic swelling and elevated Pmaip levels remained. We analysed the effect of either early or delayed treated of an antisense oligonucleotide (ASO) targeting SMN2 on a range of differentially vulnerable muscles. Following ASO administration, the majority of endplates appeared fully occupied. However, there was an underlying loss of axons and endplates, which was more prevalent following a delay in treatment. There was an increase in average motor unit size following both early and delayed treatment. Together this work demonstrates the remarkably regenerative capacity of the motor neuron following Smn restoration, but highlights that recovery is incomplete. This work suggests that there is an opportunity to enhance neuromuscular junction recovery following administration of Smn-enhancing therapeutics.

Indexed as

Muscular Atrophy, SpinalTumor Suppressor Protein p53AnimalsDisease Models, AnimalMiceMotor NeuronsOligonucleotidesOligonucleotides, AntisenseSurvival of Motor Neuron 1 ProteinOligonucleotidesOligonucleotides, AntisenseSurvival of Motor Neuron 1 ProteinTumor Suppressor Protein p53

Identifiers

PMID35551393
PMCPMC9476628
OpenAlexW4226305007

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.