Evidence map›Paper›PMID 17049594›Full record

ArticleBiomaterials2007

Cell adaptation to a physiologically relevant ECM mimic with different viscoelastic properties.

Kaustabh Ghosh, Zhi Pan, E Guan, Shouren Ge, Yajie Liu, Toshio Nakamura, Xiang-Dong Ren, Miriam Rafailovich, Richard A F Clark

Abstract read
In one paragraph

Article in Biomaterials, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing 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

138 citing papers in PubMed.

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  19. Extracellular matrix composition alters endothelial force transmission.American journal of physiology. Cell physiology · 2023
    Article
  20. Article

78 more citing papers are in PubMed but not listed here.

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

9 authors.

Kaustabh GhoshDepartment of Biomedical Engineering, SUNY at Stony Brook, Stony Brook, New York 11794-8165, USA.
Zhi Pan
E Guan
Shouren Ge
Yajie Liu
Toshio Nakamura
Xiang-Dong Ren
Miriam Rafailovich
Richard A F Clark

Funding

FIBRONECTIN AND CELL RECRUITMENTR37AG010143 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST · 1996 to 2005
$2.4M
Fibronectin mediated cell migration: signal integrationK01AR047894 · NIAMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI REN, XIANG-DONG D · 2001 to 2005
$637k
FIBRONECTIN AND CELL RECRUITMENTR01AG010143 · NIA · STATE UNIVERSITY NEW YORK STONY BROOK · PI CLARK, RICHARD AUGUST · 1991 to 1996
–
NIAMS NIH HHS AR47894NIAMS NIH HHS K01 AR047894NIA NIH HHS AG010143NIA NIH HHS R37 AG010143
6 · The paper itself

Abstract

To successfully induce tissue repair or regeneration in vivo, bioengineered constructs must possess both optimal bioactivity and mechanical strength. This is because cell interaction with the extracellular matrix (ECM) produces two different but concurrent signaling mechanisms: ligation-induced signaling, which depends on ECM biological stimuli, and traction-induced signaling, which depends on ECM mechanical stimuli. In this report, we provide a fundamental understanding of how alterations in mechanical stimuli alone, produced by varying the viscoelastic properties of our bioengineered construct, modulate phenotypic behavior at the whole-cell level. Using a physiologically relevant ECM mimic composed of hyaluronan and fibronectin, we found that adult human dermal fibroblasts modify their mechanical response in order to match substrate stiffness. More specifically, the cells on stiffer substrates had higher modulus and a more stretched and organized actin cytoskeleton (and vice versa), which translated into larger traction forces exerted on the substrate. This modulation of cellular mechanics had contrasting effects on migration and proliferation, where cells migrated faster on softer substrates while proliferating preferentially on the stiffer ones. These findings implicate substrate rigidity as a critical design parameter in the development of bioengineered constructs aimed at eliciting maximal cell and tissue function.

Indexed as

Adaptation, BiologicalActinsBiomimetic MaterialsCell MovementCell ProliferationCells, CulturedCytoskeletonElasticityExtracellular MatrixHumansMicroscopy, Atomic ForceSkinViscosityActins

Identifiers

PMID17049594
PMCPMC3625367

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.