Evidence map›Paper›PMID 27600605›Full record

ArticleTissue engineering. Part A2016

Human Corneal Fibroblast Pattern Evolution and Matrix Synthesis on Mechanically Biased Substrates.

Ramin Zareian, Monica E Susilo, Jeffrey A Paten, James P McLean, Joseph Hollmann, Dimitrios Karamichos, Conor S Messer, Dhananjay T Tambe, Nima Saeidi, James D Zieske and 1 more

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Article
  5. Keratocyte mechanobiology.Experimental eye research · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

11 authors.

Ramin Zareian1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.
Monica E Susilo1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.
Jeffrey A Paten1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.
James P McLean2 Department of Electrical and Computer Engineering, Northeastern University , Boston, Massachusetts.
Joseph Hollmann3 The Institute of Photonic Sciences , Castelldefels (Barcelona), Spain .
Dimitrios Karamichos4 Department of Ophthalmology, Dean McGee Eye Institute, Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Conor S Messer1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.
Dhananjay T Tambe5 Departments of Mechanical Engineering and Department of Pharmacology and Center for Lung Biology, University of South Alabama , Mobile, Alabama.
Nima Saeidi6 Department of Surgery, Harvard Medical School , Boston, Massachusetts.
James D Zieske7 Schepens Eye Research Institute , Boston, Massachusetts.
Jeffrey W Ruberti1 Department of Bioengineering, Northeastern University , Boston, Massachusetts.

Funding

VISION RESEARCHP30EY003790 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI Patricia Ann D'Amore · 1985 to 2026
$25.5M
CORNEAL STROMAL-EPITHELIAL INTERACTIONS DURING REPAIRR01EY005665 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI Joseph B. Ciolino · 1985 to 2026
$14.4M
NEI NIH HHS P30 EY003790NEI NIH HHS R01 EY005665
6 · The paper itself

Abstract

In a fibroblast colony model of corneal stromal development, we asked how physiological tension influences the patterning dynamics of fibroblasts and the orientation of deposited extracellular matrix (ECM). Using long-term live-cell microscopy, enabled by an optically accessible mechanobioreactor, a primary human corneal fibroblast colony was cultured on three types of substrates: a mechanically biased, loaded, dense, disorganized collagen substrate (LDDCS), a glass coverslip, and an unloaded, dense, disorganized collagen substrate (UDDCS). On LDDCS, fibroblast orientation and migration along a preferred angle developed early, cell orientation was correlated over long distances, and the colony pattern was stable. On glass, fibroblast orientation was poorly correlated, developed more slowly, and colony patterns were metastable. On UDDCS, cell orientation was correlated over shorter distances compared with LDDCS specimens. On all substrates, the ECM pattern reflected the cell pattern. In summary, mechanically biasing the collagen substrate altered the early migration behavior of individual cells, leading to stable emergent cell patterning, which set the template for newly synthesized ECM.

Indexed as

Cell MovementCollagenCorneaExtracellular MatrixFibroblastsHumansCollagen

Identifiers

PMID27600605
PMCPMC5073220

What OpenQuestion holds

Textmetadata
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.