Evidence map›Paper›PMID 22979988›Full record

ArticleBiomaterials2012

Effect of modulating macrophage phenotype on peripheral nerve repair.

Nassir Mokarram, Alishah Merchant, Vivek Mukhatyar, Gaurangkumar Patel, Ravi V Bellamkonda

Abstract read
In one paragraph

Article in Biomaterials, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

174 citing papers in PubMed, 328 citations in OpenAlex.

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114 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Nassir MokarramWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30332, USA.
Alishah Merchant
Vivek Mukhatyar
Gaurangkumar Patel
Ravi V Bellamkonda
Georgia Institute of Technology · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Bioengineered Scaffolds for Peripheral Nerve RepairR01NS044409 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI BELLAMKONDA, RAVI V. · 2002 to 2010
$2.2M
A Rational Approach to Stimulating Peripheral Nerve Regeneration Across CriticallR01NS065109 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI BELLAMKONDA, RAVI V. · 2009 to 2013
$1.6M
Fiber-Enhanced Nerve GuideR41NS067771 · NINDS · REGENERATION MATRIX, LLC · PI BELLAMKONDA, RAVI V. · 2010 to 2010
$199k
NINDS NIH HHS 1R41NS06777-1NINDS NIH HHS NS44409NINDS NIH HHS NS65109NINDS NIH HHS R01 NS044409NINDS NIH HHS R01 NS065109NINDS NIH HHS R41 NS067771
6 · The paper itself

Abstract

Peripheral nerve repair across long gaps remains clinically challenging despite progress made with autograft transplantation. While scaffolds that present trophic factors and extracellular matrix molecules have been designed, matching the performance of autograft-induced repair has been challenging. In this study, we explored the effect of cytokine mediated 'biasing' of macrophage phenotypes on Schwann cell (SC) migration and axonal regeneration in vitro and in vivo. Macrophage phenotype was successfully modulated by local delivery of either Interferon-gamma (IFN-γ) or Interleukin-4 (IL-4) within polymeric nerve guidance channels, polarizing them toward pro-inflammatory (M1) or pro-healing (M2a and M2c) phenotypes, respectively. The initial polarization of macrophages to M2a and M2c phenotype results in enhanced SC infiltration and substantially faster axonal growth in a critically-sized rat sciatic nerve gap model (15 mm). The ratio of pro-healing to pro-inflammatory population of macrophages (CD206+/CCR7+), defined as regenerative bias, demonstrates a linear relationship with the number of axons at the distal end of the nerve scaffolds. The present results clearly suggest that rather than the extent of macrophage presence, their specific phenotype at the site of injury regulates the regenerative outcomes.

Indexed as

Nerve RegenerationAnimalsCell LineCell MovementCell ProliferationImmunologic FactorsInterferon-gammaInterleukin-4Lectins, C-TypeMacrophagesMaleMannose-Binding LectinsMannose ReceptorPeripheral NervesPhenotypeRatsImmunologic FactorsInterferon-gammaInterleukin-4Lectins, C-TypeMannose-Binding LectinsMannose ReceptorReceptors, CCR7Receptors, Cell Surface

Identifiers

PMID22979988
PMCPMC3483037
OpenAlexW2008488746

What OpenQuestion holds

Textmetadata
LicenceTDM
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.