Evidence map›Paper›PMID 29291978›Full record

ArticleDevelopmental biology2018

Developmental and adult-specific processes contribute to de novo neuromuscular regeneration in the lizard tail.

Minami A Tokuyama, Cindy Xu, Rebecca E Fisher, Jeanne Wilson-Rawls, Kenro Kusumi, Jason M Newbern

Abstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
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  11. Utilizing comparative models in biomedical research.Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology
    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

6 authors.

Minami A TokuyamaSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Cindy XuSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Rebecca E FisherSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA; Department of Basic Medical Sciences, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA.
Jeanne Wilson-RawlsSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
Kenro KusumiSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA; Department of Basic Medical Sciences, University of Arizona College of Medicine-Phoenix, Phoenix, AZ 85004, USA.
Jason M NewbernSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA. Electronic address: jason.newbern@asu.edu.

Funding

Functions of ERK/MAPK Signaling in GABAergic Circuit DevelopmentR01NS097537 · NINDS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI NEWBERN, JASON MARSHALL · 2016 to 2020
$1.7M
ERK/MAPK regulation of cortical inhibitory interneuronsR00NS076661 · NINDS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI NEWBERN, JASON MARSHALL · 2013 to 2015
$726k
Developing the Anolis Lizard as a Model of Musculoskeletal RegenerationR21RR031305 · NCRR · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI KUSUMI, KENRO · 2010 to 2011
$413k
Connecting the proteome and transcriptome during regenerationR21AR064935 · NIAMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI KUSUMI, KENRO · 2013 to 2014
$345k
NCRR NIH HHS R21 RR031305NIAMS NIH HHS R21 AR064935NINDS NIH HHS R00 NS076661NINDS NIH HHS R01 NS097537
6 · The paper itself

Abstract

Peripheral nerves exhibit robust regenerative capabilities in response to selective injury among amniotes, but the regeneration of entire muscle groups following volumetric muscle loss is limited in birds and mammals. In contrast, lizards possess the remarkable ability to regenerate extensive de novo muscle after tail loss. However, the mechanisms underlying reformation of the entire neuromuscular system in the regenerating lizard tail are not completely understood. We have tested whether the regeneration of the peripheral nerve and neuromuscular junctions (NMJs) recapitulate processes observed during normal neuromuscular development in the green anole, Anolis carolinensis. Our data confirm robust axonal outgrowth during early stages of tail regeneration and subsequent NMJ formation within weeks of autotomy. Interestingly, NMJs are overproduced as evidenced by a persistent increase in NMJ density 120 and 250 days post autotomy (DPA). Substantial Myelin Basic Protein (MBP) expression could also be detected along regenerating nerves indicating that the ability of Schwann cells to myelinate newly formed axons remained intact. Overall, our data suggest that the mechanism of de novo nerve and NMJ reformation parallel, in part, those observed during neuromuscular development. However, the prolonged increase in NMJ number and aberrant muscle differentiation hint at processes specific to the adult response. An examination of the coordinated exchange between peripheral nerves, Schwann cells, and newly synthesized muscle of the regenerating neuromuscular system may assist in the identification of candidate molecules that promote neuromuscular recovery in organisms incapable of a robust regenerative response.

Indexed as

AnimalsAxonsBungarotoxinsFluorescent DyesLizardsMotor NeuronsMuscle, SkeletalMyelin SheathNerve RegenerationNeuromuscular JunctionRegenerationSchwann CellsTailBungarotoxinsFluorescent Dyesde novoLizardNeuromuscular junctionRegenerationReptile

Identifiers

PMID29291978
PMCPMC5764105

What OpenQuestion holds

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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.