Evidence map›Paper›PMID 23099064›Full record

ArticleBiomaterials2013

Directing cell migration in continuous microchannels by topographical amplification of natural directional persistence.

Young-Gwang Ko, Carlos C Co, Chia-Chi Ho

Abstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Crosshatch nanofiber networks of tunable interfiber spacing induce plasticity in cell migration and cytoskeletal response.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Article
  9. Engineering Dynamic Biointerfaces.Current opinion in chemical engineering · 2016
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. 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

3 authors.

Young-Gwang KoDepartment of Chemical and Materials Engineering, University of Cincinnati, Cincinnati, OH 45220, USA.
Carlos C Co
Chia-Chi Ho

Funding

One Way Micropatterns for Self-Assembly and Sorting of CellsR01EB010043 · NIBIB · UNIVERSITY OF CINCINNATI · PI HO, CHIA-CHI · 2010 to 2013
$1.3M
NIBIB NIH HHS R01 EB010043NIBIB NIH HHS R01EB010043
6 · The paper itself

Abstract

Discrete micropatterns on biomaterial surfaces can be used to guide the direction of mammalian cell movement by orienting cell morphology. However, guiding cell assembly in three-dimensional scaffolds remains a challenge. Here we demonstrate that the random motions of motile cells can be rectified within continuous microchannels without chemotactic gradients or fluid flow. Our results show that uniform width microchannels with an overhanging zigzag design can induce polarization of NIH3T3 fibroblasts and human umbilical vein endothelial cells by expanding the cell front at each turn. These continuous zigzag microchannels can guide the direction of cell movement even for cells with altered intracellular signals that promote random movement. This approach for directing cell migration within microchannels has important potential implications in the design of scaffolds for tissue engineering.

Indexed as

Cell MovementAnimalsBiocompatible MaterialsFibroblastsGelatinGTP PhosphohydrolasesHumansHuman Umbilical Vein Endothelial CellsMiceNIH 3T3 CellsSurface PropertiesTissue EngineeringTissue ScaffoldsBiocompatible MaterialsGelatinGTP Phosphohydrolases

Identifiers

PMID23099064
PMCPMC3591109

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.