Evidence map›Paper›PMID 24781157›Full record

ArticleLab on a chip2014

Small-molecule axon-polarization studies enabled by a shear-free microfluidic gradient generator.

Hui Xu, Meghaan M Ferreira, Sarah C Heilshorn

Abstract read
In one paragraph

Article in Lab on a chip, 2014. 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. Review
  2. Engineering Sensory Ganglion Multicellular System to Model Tissue Nerve Ingrowth.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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  4. Review
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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.

Hui XuDepartment of Materials Science and Engineering, Stanford Cardiovascular Institute, Stanford University, 476 Lomita Mall, McCullough Building, Stanford, CA 94305-4045, USA. heilshorn@stanford.edu.
Meghaan M Ferreira
Sarah C Heilshorn

Funding

T32 Training Program in Mechanisms and Innovation in Vascular DiseaseT32HL098049 · NHLBI · STANFORD UNIVERSITY · PI Nicholas James Leeper, Philip S Tsao · 2010 to 2026
$6.3M
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
NHLBI NIH HHS 1T32-HL098049-01A1NHLBI NIH HHS T32 HL098049NIAMS NIH HHS R21 AR062359NIAMS NIH HHS R21-AR062359NIDDK NIH HHS R01 DK085720NIDDK NIH HHS R01-DK085720NIH HHS DP2 OD006477NIH HHS DP2-OD006477-01
6 · The paper itself

Abstract

A deep understanding of the mechanisms behind neurite polarization and axon path-finding is important for interpreting how the human body guides neurite growth during development and response to injury. Further, it is of great clinical importance to identify diffusible chemical cues that promote neurite regeneration for nervous tissue repair. Despite the fast development of various types of concentration gradient generators, it has been challenging to fabricate neuron-friendly (i.e. shear-free and biocompatible for neuron growth and maturation) devices to create stable gradients, particularly for fast diffusing small molecules, which typically require high flow and shear rates. Here we present a finite element analysis for a polydimethylsiloxane/polyethylene glycol diacrylate (PDMS/PEG-DA) based gradient generator, describe the microfabrication process, and validate its use for neuronal axon polarization studies. This device provides a totally shear-free, biocompatible microenvironment with a linear and stable concentration gradient of small molecules such as forskolin. The gradient profile in this device can be customized by changing the composition or width of the PEG-DA barriers during direct UV photo-patterning within a permanently bonded PDMS device. Primary rat cortical neurons (embryonic E18) exposed to soluble forskolin gradients for 72 h exhibited statistically significant polarization and guidance of their axons. This device provides a useful platform for both chemotaxis and directional guidance studies, particularly for shear sensitive and non-adhesive cell cultures, while allowing fast new device design prototyping at a low cost.

Indexed as

AxonsMicrofluidic Analytical TechniquesAdjuvants, ImmunologicAnimalsCell Culture TechniquesCerebral CortexColforsinDimethylpolysiloxanesHumansMaterials TestingNylonsPolyethylene GlycolsRatsRats, Sprague-DawleyAdjuvants, ImmunologicColforsinDimethylpolysiloxanesNylonspoly(dimethylsiloxane)-polyamide copolymerpoly(ethylene glycol)diacrylatePolyethylene Glycols

Identifiers

PMID24781157
PMCPMC4528973

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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.