Evidence map›Paper›PMID 25308870›Full record

ArticleActa biomaterialia2015

Matrix RGD ligand density and L1CAM-mediated Schwann cell interactions synergistically enhance neurite outgrowth.

Nicole H Romano, Christopher M Madl, Sarah C Heilshorn

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  16. Tissue Models for Neurogenesis and Repair in 3D.Advanced functional materials · 2018
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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

3 authors at 1 institution in 1 country.

Nicole H RomanoMaterials Science and Engineering Department, Stanford University, Stanford, CA 94305, USA.
Christopher M MadlBioengineering Department, Stanford University, Stanford, CA 94305, USA.
Sarah C HeilshornMaterials Science and Engineering Department, Stanford University, Stanford, CA 94305, USA. Electronic address: heilshorn@stanford.edu.
Stanford University · US

Funding

Three-dimensional Scaffold-based Systems for Primary Human Intestinal CultureR01DK085720 · NIDDK · STANFORD UNIVERSITY · PI KUO, CALVIN J · 2009 to 2013
$3.7M
Engineering 3D in vitro niches to reveal fundamentals of cellular biomechanicsDP2OD006477 · OD · STANFORD UNIVERSITY · PI HEILSHORN, SARAH C · 2009 to 2009
$2.4M
3D Bioengineering Strategies to Mimic Human Skeletal Muscle Progenitor Cell NicheR21AR062359 · NIAMS · STANFORD UNIVERSITY · PI BLAU, HELEN M, HEILSHORN, SARAH C · 2011 to 2012
$367k
NIAMS NIH HHS R21 AR062359NIAMS NIH HHS R21-AR062359-01NIDDK NIH HHS R01 DK085720NIDDK NIH HHS R01-DK085720NIH HHS 1DP2-OD006477NIH HHS DP2 OD006477
6 · The paper itself

Abstract

The innate biological response to peripheral nerve injury involves a complex interplay of multiple molecular cues to guide neurites across the injury gap. Many current strategies to stimulate regeneration take inspiration from this biological response. However, little is known about the balance of cell-matrix and Schwann cell-neurite dynamics required for regeneration of neural architectures. We present an engineered extracellular matrix (eECM) microenvironment with tailored cell-matrix and cell-cell interactions to study their individual and combined effects on neurite outgrowth. This eECM regulates cell-matrix interactions by presenting integrin-binding RGD (Arg-Gly-Asp) ligands at specified densities. Simultaneously, the addition or exclusion of nerve growth factor (NGF) is used to modulate L1CAM-mediated Schwann cell-neurite interactions. Individually, increasing the RGD ligand density from 0.16 to 3.2mM resulted in increasing neurite lengths. In matrices presenting higher RGD ligand densities, neurite outgrowth was synergistically enhanced in the presence of soluble NGF. Analysis of Schwann cell migration and co-localization with neurites revealed that NGF enhanced cooperative outgrowth between the two cell types. Interestingly, neurites in NGF-supplemented conditions were unable to extend on the surrounding eECM without the assistance of Schwann cells. Blocking studies revealed that L1CAM is primarily responsible for these Schwann cell-neurite interactions. Without NGF supplementation, neurite outgrowth was unaffected by L1CAM blocking or the depletion of Schwann cells. These results underscore the synergistic interplay between cell-matrix and cell-cell interactions in enhancing neurite outgrowth for peripheral nerve regeneration.

Indexed as

AnimalsAvian ProteinsCells, CulturedChick EmbryoExtracellular MatrixNeural Cell Adhesion Molecule L1NeuritesOligopeptidesSchwann Cellsarginyl-glycyl-aspartic acidAvian ProteinsNeural Cell Adhesion Molecule L1OligopeptidesDorsal root gangliaElastin-like peptideL1CAMNerve growth factorRGD ligands

Identifiers

PMID25308870
PMCPMC4528982
OpenAlexW1990474391

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.