Evidence map›Paper›PMID 29147681›Full record

ArticleACS biomaterials science & engineering2017

Crimped Nanofibrous Biomaterials Mimic Microstructure and Mechanics of Native Tissue and Alter Strain Transfer to Cells.

Spencer E Szczesny, Tristan P Driscoll, Hsiao-Yun Tseng, Pang-Ching Liu, Su-Jin Heo, Robert L Mauck, Pen-Hsiu G Chao

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
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  8. Mechanoepigenetic regulation of extracellular matrix homeostasis via Yap and Taz.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  16. Boost Tendon/Ligament Repair With Biomimetic and Smart Cellular Constructs.Frontiers in bioengineering and biotechnology · 2021
    Review
  17. Article
  18. Review
  19. Article
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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

7 authors.

Spencer E SzczesnyMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, United States.
Tristan P DriscollMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, United States.
Hsiao-Yun TsengInstitute of Biomedical Engineering, School of Medicine and School of Engineering, National Taiwan University, Taipei 10617, Taiwan.
Pang-Ching LiuInstitute of Biomedical Engineering, School of Medicine and School of Engineering, National Taiwan University, Taipei 10617, Taiwan.
Su-Jin HeoMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, United States.
Robert L MauckMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, Philadelphia, Pennsylvania 19104, United States.
Pen-Hsiu G ChaoInstitute of Biomedical Engineering, School of Medicine and School of Engineering, National Taiwan University, Taipei 10617, Taiwan.

Funding

Dynamic Fibrous Scaffolds for Repairing Dense Connective TissuesR01AR056624 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Jason A Burdick, Robert L Mauck · 2009 to 2026
$7.5M
The Role of Hyaluronic Acid Receptors in Tendon HealingP30AR050950 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI BALDWIN, DONALD A · 2006 to 2015
$6.2M
Training in Muscle Biology and Muscle DiseaseT32AR053461 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI OSTAP, E. MICHAEL · 2006 to 2025
$4.9M
Role of Mechanical Loading and Stem Cell Mechanotransduction in Tendon DegenerationF32AR070562 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI SZCZESNY, SPENCER · 2016 to 2017
$65k
NIAMS NIH HHS F32 AR070562NIAMS NIH HHS P30 AR050950NIAMS NIH HHS R01 AR056624NIAMS NIH HHS T32 AR053461
6 · The paper itself

Abstract

To fully recapitulate tissue microstructure and mechanics, fiber crimping must exist within biomaterials used for tendon/ligament engineering. Existing crimped nanofibrous scaffolds produced via electrospinning are dense materials that prevent cellular infiltration into the scaffold interior. In this study, we used a sacrificial fiber population to increase the scaffold porosity and evaluated the effect on fiber crimping. We found that increasing scaffold porosity increased fiber crimping and ensured that the fibers properly uncrimped as the scaffolds were stretched by minimizing fiber-fiber interactions. Constitutive modeling demonstrated that the fiber uncrimping produced a nonlinear mechanical behavior similar to that of native tendon and ligament. Interestingly, fiber crimping altered strain transmission to the nuclei of cells seeded on the scaffolds, which may account for previously observed changes in gene expression. These crimped biomaterials are useful for developing functional fiber-reinforced tissues and for studying the effects of altered fiber crimping due to damage or degeneration.

Indexed as

crimpelectrospinningligamentmodelingtendontissue engineering

Identifiers

PMID29147681
PMCPMC5683713

What OpenQuestion holds

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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.