Evidence map›Paper›PMID 37612637›Full record

ArticleBMC neuroscience2023

Enhancing structural plasticity of PC12 neurons during differentiation and neurite regeneration with a catalytically inactive mutant version of the zRICH protein.

Ashoka C Bandla, Aditya S Sheth, Sara M Zarate, Suraj Uskamalla, Elizabeth C Hager, Victor A Villarreal, Maribel González-García, Rafael P Ballestero

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Ashoka C BandlaDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA.
Aditya S ShethDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA.
Sara M ZarateDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA.
Suraj UskamallaDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA.
Elizabeth C HagerDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA.
Victor A VillarrealDepartment of Chemistry, Texas A&M University-Kingsville, Kingsville, TX, 78363, USA.
Maribel González-GarcíaDepartment of Chemistry, Texas A&M University-Kingsville, Kingsville, TX, 78363, USA.
Rafael P BallesteroDepartment of Biological and Health Sciences, Texas A&M University-Kingsville, 700 University Blvd, Kingsville, TX, 78363, USA. karp002@tamuk.edu.
Texas A&M University – Kingsville · US

Funding

Enhancement of Neuronal Plasticity and Axon Regeneration Capabilities of Pro-NeurSC3GM109785 · NIGMS · TEXAS A&M UNIVERSITY-KINGSVILLE · PI PEREZ-BALLESTERO, RAFAEL · 2014 to 2017
$414k
NIGMS NIH HHS SC3 GM109785
6 · The paper itself

Abstract

backgroundStudies of the molecular mechanisms of nerve regeneration have led to the discovery of several proteins that are induced during successful nerve regeneration. RICH proteins were identified as proteins induced during the regeneration of the optic nerve of teleost fish. These proteins are 2',3'-cyclic nucleotide, 3'-phosphodiesterases that can bind to cellular membranes through a carboxy-terminal membrane localization domain. They interact with the tubulin cytoskeleton and are able to enhance neuronal structural plasticity by promoting the formation of neurite branches.

resultsPC12 stable transfectant cells expressing a fusion protein combining a red fluorescent protein with a catalytically inactive mutant version of zebrafish RICH protein were generated. These cells were used as a model to analyze effects of the protein on neuritogenesis. Differentiation experiments showed a 2.9 fold increase in formation of secondary neurites and a 2.4 fold increase in branching points. A 2.2 fold increase in formation of secondary neurites was observed in neurite regeneration assays.

conclusionsThe use of a fluorescent fusion protein facilitated detection of expression levels. Two computer-assisted morphometric analysis methods indicated that the catalytically inactive RICH protein induced the formation of branching points and secondary neurites both during differentiation and neurite regeneration. A procedure based on analysis of random field images provided comparable results to classic neurite tracing methods.

Indexed as

NeuritesZebrafishAnimalsCell DifferentiationNerve RegenerationNeurons2’,3’-Cyclic Nucleotide 3’-PhosphodiesteraseAxon RegenerationNeuritogenesisNeuron differentiationTeleost

Identifiers

PMID37612637
PMCPMC10463786
OpenAlexW4386098041

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.