Evidence map›Paper›PMID 25219769›Full record

ArticleActa biomaterialia2015

Oriented matrix promotes directional tubulogenesis.

Patricia A Soucy, Maria Hoh, Will Heinz, Jan Hoh, Lewis Romer

Abstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Patricia A SoucyDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Bioengineering, University of Louisville, Louisville, KY 40292, USA.
Maria HohIntelligent Substrates, Inc., Sykesville, MD, USA.
Will HeinzIntelligent Substrates, Inc., Sykesville, MD, USA; Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Jan HohDepartment of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Lewis RomerDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Anesthesiology and Critical Care Medicine, Cell Biology, and Pediatrics, and the Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Funding

Endothelial Progenitor Cells for Lung RepairK18HL088203 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI ROMER, LEWIS H · 2007 to 2008
$368k
Tissue Engineering Application to Craniofacial DefectsF31DE016544 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI ARAUZ, PATRICIA S · 2006 to 2008
$117k
NHLBI NIH HHS HL088203NHLBI NIH HHS K18 HL088203NIDCR NIH HHS DE016544NIDCR NIH HHS F31 DE016544
6 · The paper itself

Abstract

Detailed control over the structural organization of scaffolds and engineered tissue constructs is a critical need in the quest to engineer functional tissues using biomaterials. This work presents a new approach to spatially direct endothelial tubulogenesis. Micropatterned fibronectin substrates were used to control lung fibroblast adhesion and growth and the subsequent deposition of fibroblast-derived matrix during culture. The fibroblast-derived matrix produced on the micropatterned substrates was tightly oriented by these patterns, with an average variation of only 8.5°. Further, regions of this oriented extracellular matrix provided directional control of developing endothelial tubes to within 10° of the original micropatterned substrate design. Endothelial cells seeded directly onto the micropatterned substrate did not form tubes. A metric for matrix anisotropy showed a relationship between the fibroblast-derived matrix and the endothelial tubes that were subsequently developed on the same micropatterns with a resulting aspect ratio over 1.5 for endothelial tubulogenesis. Micropatterns in "L" and "Y" shapes were used to direct endothelial tubes to turn and branch with the same level of precision. These data demonstrate that anisotropic fibroblast-derived matrices instruct the alignment and shape of endothelial tube networks, thereby introducing an approach that could be adapted for future design of microvascular implants featuring organ-specific natural matrix that patterns microvascular growth.

Indexed as

Tissue ScaffoldsAnisotropyBiomimetic MaterialsCell LineCell PolarityCells, CulturedEndothelial CellsEquipment DesignEquipment Failure AnalysisExtracellular MatrixFibroblastsGuided Tissue RegenerationHumansMaterials TestingMicrovesselsNeovascularization, PhysiologicAnisotropyEndothelial morphogenesisExtracellular matrixMicropattern substrate

Identifiers

PMID25219769
PMCPMC4256113

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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.