Evidence map›Paper›PMID 8702006›Full record

ArticleThe American journal of pathology1996

Serum stimulation, cell-cell interactions, and extracellular matrix independently influence smooth muscle cell phenotype in vitro.

S Kato, J R Shanley, J C Fox

Abstract read
In one paragraph

Article in The American journal of pathology, 1996. 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
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  8. Timing of ICAM-I Expression in a Canine Model of Post-Haemorrhagic Cerebral Vasospasm.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2000
    Article
  9. 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

3 authors at 1 institution in 1 country.

S KatoDepartment of Medicine, University of Pennsylvania, Philadelphia 19104-6069, USA.
J R Shanley
J C Fox
University of Pennsylvania · US

Funding

FIBROBLAST GROWTH FACTORS AND STRIATED MUSCLER37HL026831 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SWAIN, JUDITH L. · 1992 to 2001
$682k
FGF'S AND THE CONTROL OF SMOOTH MUSCLE CELL GROWTHK08HL002939 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI FOX, JONATHAN C · 1993 to 1997
–
MYOCARDIAL FUNCTION AND METABOLISM DURING ISCHEMIAR01HL026831 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SWAIN, JUDITH L. · 1985 to 1993
–
NHLBI NIH HHS HL02939NHLBI NIH HHS HL26831
6 · The paper itself

Abstract

Vascular injury profoundly alters the vessel wall microenvironment, and smooth muscle cells respond with cell cycle re-entry, loss of contractile elements, extracellular matrix remodeling, and altered signaling by endogenous growth factors and their receptors. Environmental cues include stimulation by exogenous mitogens and both cell-cell and cell-matrix interactions. Modeling this process in smooth muscle cells in vitro, these environmental determinants were varied independently and the phenotypic consequences assessed. Mitogenic stimulation with serum promoted the synthesis of collagen and fibronectin and the expression of fibroblast growth factor receptor-1 and suppressed the content of smooth muscle alpha-actin, myosin heavy chain, and basic fibroblast growth factor. Low cell density (reduced cell-cell contact) was also associated with enhanced extracellular matrix protein production, increased fibroblast growth factor receptor-1 expression, and reduced contractile protein and basic fibroblast growth factor content. The influence of serum stimulation and reduced cell-cell contact were independent and additive. Provision of a type I collagen matrix blunted the influence of serum and cell-cell contact on collagen synthesis but had minor effects on other measures of phenotype. Environmental factors thus independently influence smooth muscle cell phenotype, including endogenous growth factor expression and responsiveness, which can in turn influence the microenvironment of the vessel wall after injury.

Indexed as

Blood Physiological PhenomenaActinsAnimalsAortaBlotting, WesternCell CommunicationCell CycleCells, CulturedCollagenExtracellular MatrixFibroblast Growth Factor 2FibronectinsMuscle, Smooth, VascularMyosin Heavy ChainsPhenotypeRatsActinsCollagenFibroblast Growth Factor 2FibronectinsMyosin Heavy ChainsReceptors, Fibroblast Growth Factor

Identifiers

PMID8702006
PMCPMC1865314
OpenAlexW1854686051

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.