Evidence map›Paper›PMID 20625538›Full record

ArticleCellular and molecular bioengineering2009

Optimization by Response Surface Methodology of Confluent and Aligned Cellular Monolayers for Nerve Guidance.

Celinda M Kofron, Diane Hoffman-Kim

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. A sequential multimodal framework for spinal cord regeneration.Frontiers in cellular neuroscience · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Topography, cell response, and nerve regeneration.Annual review of biomedical engineering · 2010
    Review
  8. Neurite outgrowth at the biomimetic interface.Annals of biomedical engineering · 2010
    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

2 authors at 1 institution in 1 country.

Celinda M KofronDepartment of Molecular Pharmacology, Physiology, and Biotechnology and Center for Biomedical Engineering, Brown University, Box G-B387, Providence, RI 02912, USA.
Diane Hoffman-Kim
Brown University · US

Funding

Quantifying Axon Growth in Complex EnvironmentsR01EB005722 · NIBIB · BROWN UNIVERSITY · PI HOFFMAN-KIM, DIANE · 2007 to 2010
$1.3M
NIBIB NIH HHS R01 EB005722
6 · The paper itself

Abstract

Anisotropic tissue structures provide guidance for navigating neurons in vitro and in vivo. Here we optimized the generation of comparable anisotropic monolayers of astrocytes, endothelial cells, and Schwann cells as a first step toward determining which properties of anisotropic cells are sufficient for nerve guidance. The statistical experimental design method Design of Experiments and the experimental analysis method Response Surface Methodology were applied to improve efficiency and utility. Factors investigated included dimensions of microcontact printed protein patterns, cell density, and culture duration. Protein patterning spacing had the strongest influence. When cells initially aligned at borders and proliferated to fill in spaces, space between stripes was most effective when it was comparable to cell size. Maximizing the area of adhesive molecule coverage was also important for confluence of these types of cells. When cells adhered and aligned over the width of a stripe and broadened to fill spaces, space width about half the cell width was most effective. These findings suggest that if the mechanism of alignment, alignment at borders or over the width of the stripe, is predetermined and the cell size determined, the optimal size of the micropatterning for aligned monolayers of other cell types can be predicted. This study also demonstrates the effective use of DOE and RSM to probe cellular responses to various and multiple factors toward determination of optimal conditions for a desired cellular response.

Identifiers

PMID20625538
PMCPMC2901170
OpenAlexW1974281773

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.