Evidence map›Paper›PMID 22325251›Full record

ArticleProteome science2012

Spatiotemporal expression profiling of proteins in rat sciatic nerve regeneration using reverse phase protein arrays.

David J Bryan, C Robert Litchfield, Jeffrey V Manchio, Tanya Logvinenko, Antonia H Holway, John Austin, Ian C Summerhayes, Kimberly M Rieger-Christ

Open access · goldAbstract read
In one paragraph

Article in Proteome science, 2012. 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
1.1field-weighted citation impact, top 23% 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, 28 citations in OpenAlex.

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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 2 institutions in 1 country.

David J Bryan *Tissue Engineering Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
C Robert Litchfield *Tissue Engineering Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
Jeffrey V ManchioTissue Engineering Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
Tanya LogvinenkoInstitute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, Massachusetts, USA.
Antonia H HolwayIan C. Summerhayes Cell and Molecular Biology Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
John AustinAushon BioSystems Inc., Billerica, Massachusetts, USA.
Ian C SummerhayesIan C. Summerhayes Cell and Molecular Biology Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
Kimberly M Rieger-ChristIan C. Summerhayes Cell and Molecular Biology Laboratory, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
Lahey Hospital and Medical Center · USTufts Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein expression profiles throughout 28 days of peripheral nerve regeneration were characterized using an established rat sciatic nerve transection injury model. Reverse phase protein microarrays were used to identify the spatial and temporal expression profile of multiple proteins implicated in peripheral nerve regeneration including growth factors, extracellular matrix proteins, and proteins involved in adhesion and migration. This high-throughput approach enabled the simultaneous analysis of 3,360 samples on a nitrocellulose-coated slide.

resultsThe extracellular matrix proteins collagen I and III, laminin gamma-1, fibronectin, nidogen and versican displayed an early increase in protein levels in the guide and proximal sections of the regenerating nerve with levels at or above the baseline expression of intact nerve by the end of the 28 day experimental course. The 28 day protein levels were also at or above baseline in the distal segment however an early increase was only noted for laminin, nidogen, and fibronectin. While the level of epidermal growth factor, ciliary neurotrophic factor and fibroblast growth factor-1 and -2 increased throughout the experimental course in the proximal and distal segments, nerve growth factor only increased in the distal segment and fibroblast growth factor-1 and -2 and nerve growth factor were the only proteins in that group to show an early increase in the guide contents. As expected, several proteins involved in cell adhesion and motility; namely focal adhesion kinase, N-cadherin and β-catenin increased earlier in the proximal and distal segments than in the guide contents reflecting the relatively acellular matrix of the early regenerate.

conclusionsIn this study we identified changes in expression of multiple proteins over time linked to regeneration of the rat sciatic nerve both demonstrating the utility of reverse phase protein arrays in nerve regeneration research and revealing a detailed, composite spatiotemporal expression profile of peripheral nerve regeneration.

Identifiers

PMID22325251
PMCPMC3295716
OpenAlexW2144088298

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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.