Evidence map›Paper›PMID 31127156›Full record

ArticleScientific reports2019

Nerve sprouting capacity in a pharmacologically induced mouse model of spinal muscular atrophy.

Mendell Rimer, Bonnie L Seaberg, Pei-Fen Yen, Steven Lam, Robert Louis Hastings, Young Il Lee, Wesley J Thompson, Zhihua Feng, Friedrich Metzger, Sergey Paushkin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. AAV9-DOK7 gene therapy reduces disease severity in SmnBiochemical and biophysical research communications · 2020
    Article
  5. 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

11 authors at 4 institutions in 2 countries.

Mendell RimerDepartment of Neuroscience and Experimental Therapeutics Texas A & M University Health Science Center, Bryan, TX, USA. mjrimer@medicine.tamhsc.edu.
Bonnie L SeabergDepartment of Neuroscience and Experimental Therapeutics Texas A & M University Health Science Center, Bryan, TX, USA.
Pei-Fen YenSection of Neurobiology Department of Biological Sciences University of Southern California, Los Angeles, CA, USA.
Steven LamSection of Neurobiology Department of Biological Sciences University of Southern California, Los Angeles, CA, USA.
Robert Louis HastingsDepartment of Biology Texas A & M University, College Station, TX, USA.
Young Il LeeDepartment of Biology Texas A & M University, College Station, TX, USA.ORCID http://orcid.org/0000-0003-4993-9038
Wesley J ThompsonDepartment of Biology Texas A & M University, College Station, TX, USA.
Zhihua FengSection of Neurobiology Department of Biological Sciences University of Southern California, Los Angeles, CA, USA.
Friedrich MetzgerRoche Pharmaceutical Research and Early Development, Roche Innovation Center Basel, Basel, Switzerland.
Sergey PaushkinSMA Foundation, New York, NY, USA.
Chien-Ping KoSection of Neurobiology Department of Biological Sciences University of Southern California, Los Angeles, CA, USA. cko@usc.edu.
University of Southern California · USTexas A&M University · USTexas A&M Health Science Center · USRoche (Switzerland) · CH

Funding

SYNAPSE ELIMINATION IN NEONATAL SKELETAL MUSCLER01NS020480 · NINDS · UNIVERSITY OF TEXAS AUSTIN · PI MCMAHAN, UEL J · 1985 to 2019
$2.8M
NINDS NIH HHS R01 NS020480
6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is caused by loss-of-function mutations in the survival of motoneuron gene 1 (SMN1). SMA is characterized by motoneuron death, skeletal muscle denervation and atrophy. Disease severity inversely correlates with copy number of a second gene (SMN2), which harbors a splicing defect that causes the production of inadequate levels of functional SMN protein. Small molecules that modify SMN2 splicing towards increased production of functional SMN significantly ameliorate SMA phenotypes in mouse models of severe SMA. At suboptimal doses, splicing modifiers, such as SMN-C1, have served to generate mice that model milder SMA, referred to as pharmacological SMA mice, which survive into early adulthood. Nerve sprouting at endplates, known as terminal sprouting, is key to normal muscle fiber reinnervation following nerve injury and its promotion might mitigate neuromuscular symptoms in mild SMA. Sprouting has been difficult to study in severe SMA mice due to their short lifespan. Here, we show that pharmacological SMA mice are capable of terminal sprouting following reinnervation that is largely SMN-C1 dose-independent, but that they display a reinnervation delay that is critically SMN-C1 dose-dependent. Data also suggest that SMN-C1 can induce by itself a limited terminal sprouting response in SMA and wild-type normally-innervated endplates.

Indexed as

AnimalsDisease Models, AnimalHumansMiceMuscle Fibers, SkeletalMuscle, SkeletalMuscular Atrophy, SpinalNerve RegenerationNeuromuscular JunctionSchwann Cells

Identifiers

PMID31127156
PMCPMC6534600
OpenAlexW2946374088

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.