Evidence map›Paper›PMID 20858564›Full record

ArticleBiomaterials2011

The use of micropatterning to control smooth muscle myosin heavy chain expression and limit the response to transforming growth factor β1 in vascular smooth muscle cells.

Corin Williams, Xin Q Brown, Erzsebet Bartolak-Suki, Hongwei Ma, Ashutosh Chilkoti, Joyce Y Wong

Abstract read
In one paragraph

Article in Biomaterials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

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  18. Vascular smooth muscle contractility depends on cell shape.Integrative biology : quantitative biosciences from nano to macro · 2011
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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

6 authors at 2 institutions in 1 country.

Corin WilliamsDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Xin Q Brown
Erzsebet Bartolak-Suki
Hongwei Ma
Ashutosh Chilkoti
Joyce Y Wong
Boston University · USDuke University · US

Funding

Vascular Cell Phenotype on Physiologically-relevant Bioengineered SubstrataR01HL072900 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI WONG, JOYCE Y · 2003 to 2011
$3.6M
NHLBI NIH HHS R01 HL072900NHLBI NIH HHS R01 HL72900
6 · The paper itself

Abstract

In the healthy artery, contractile vascular smooth muscle cells (VSMCs) have an elongated shape and are highly aligned but transition to a synthetic phenotype in culture, while additionally becoming well spread and randomly organized. Thus, controlling VSMC phenotype is a challenge in tissue engineering. In this study, we investigated the effects of micropatterning on contractile protein expression in VSMCs at low and high passage and in the presence of transforming growth factor beta 1 (TGFβ1). Micropatterning led to significantly decreased cell area, increased elongation, and increased alignment compared to non-patterned VSMCs independent of passage number. In the presence of serum, micropatterning led to increased smooth muscle myosin heavy chain (SM-MHC) and α-actin expression in low passage VSMCs, but had no effect on high passage VSMCs. Micropatterning was as effective as TGFβ1 in up-regulating SM-MHC at low passage; however, micropatterning limited VSMC response to TGFβ1 at both low and high passage. Investigation of TGFβ receptor 1 revealed higher expression in non-patterned VSMCs compared to patterned at high passage. Our studies demonstrate that micropatterning is an important regulator of SM-MHC expression in contractile VSMCs and that it may provide a mechanism for phenotype stabilization in the presence of growth factors.

Indexed as

AnimalsBlotting, WesternCell Culture TechniquesCell ShapeMaleMuscle, Smooth, VascularMyocytes, Smooth MuscleMyosin Heavy ChainsPolymersRabbitsTissue EngineeringTransforming Growth Factor beta1Myosin Heavy ChainsPolymersTransforming Growth Factor beta1

Identifiers

PMID20858564
PMCPMC2991379
OpenAlexW2031273706

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.