Evidence map›Paper›PMID 25114097›Full record

ArticleCirculation research2014

Adipose stromal cells differentiate along a smooth muscle lineage pathway upon endothelial cell contact via induction of activin A.

Stephanie Merfeld-Clauss, Ivan P Lupov, Hongyan Lu, Dongni Feng, Peter Compton-Craig, Keith L March, Dmitry O Traktuev

Abstract read
PubMed Publisher
In one paragraph

Article in Circulation research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  8. Lung Microvascular Niche, Repair, and Engineering.Frontiers in bioengineering and biotechnology · 2020
    Review
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  19. The Effects of a Pulsed Electromagnetic Field on the Proliferation and Osteogenic Differentiation of Human Adipose-Derived Stem Cells.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Stephanie Merfeld-ClaussFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Ivan P LupovFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Hongyan LuFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Dongni FengFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Peter Compton-CraigFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Keith L MarchFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.).
Dmitry O TraktuevFrom Indiana Center for Vascular Biology and Medicine, Department of Medicine (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.) and Department of Cellular and Integrative Physiology (K.L.M.) at Indiana University School of Medicine, Indianapolis; and VA Center for Regenerative Medicine, Department of Research and Development at R.L. Roudebush VA Medical Center, Indianapolis, IN (S.M.-C., I.P.L., H.L., D.F., P.C.-C., K.L.M., D.O.T.). tdmitry@iu.edu.
Richard L. Roudebush VA Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleAdipose stromal cells (ASC) are therapeutically potent progenitor cells that possess properties of pericytes. In vivo, ASC in combination with endothelial cells (EC) establish functional multilayer vessels, in which ASC form the outer vessel layer and differentiate into mural cells.

objectiveTo identify factors responsible for ASC differentiation toward the smooth muscle cell phenotype via interaction with EC. METHODS AND

resultsAn in vitro model of EC cocultivation with ASC was used, in which EC organized into vascular cords, accompanied by ASC migration toward EC and upregulation of α-smooth muscle actin, SM22α, and calponin expression. Conditioned media from EC-ASC, but not from EC cultures, induced smooth muscle cell protein expression in ASC monocultures. EC-ASC cocultivation induced marked accumulation of activin A but not transforming growth factor-β1 in conditioned media. This was attributed to induction of activin A expression in ASC on contact with EC. Although transforming growth factor-β and activin A were individually sufficient to initiate expression of smooth muscle cell antigens in ASC, only activin A IgG blocked the effect of EC-ASC conditioned media. Although transforming growth factor-β was able to induce activin A expression in ASC, in cocultures this induction was transforming growth factor-β independent. In EC-ASC cocultures, activin A IgG or ALK4/5/7 receptor inhibitors blocked expression of α-smooth muscle actin in ASC in the absence of direct EC-cord contact, but this inhibition was circumvented in ASC by direct EC contact.

conclusionsEC initiate a smooth muscle cell differentiation program in adjacent ASC and propagate this differentiation in distant ASC by induction of activin A expression.

Indexed as

Cell CommunicationCell DifferentiationCell LineageActinsActivin Receptors, Type IActivinsAdipose TissueCalcium-Binding ProteinsCalponinsCell MovementCells, CulturedCoculture TechniquesEndothelial CellsFollistatinHumansMesenchymal Stem CellsACTA2 protein, humanActinsactivin AActivin Receptors, Type IActivinsACVR1B protein, humanACVR1C protein, humanCalcium-Binding ProteinsCalponinsFollistatinFST protein, humanMicrofilament ProteinsMuscle ProteinsProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type ISmad2 ProteinSMAD2 protein, humanTGFB1 protein, humanTransforming Growth Factor beta1transgelinactivin Aadipose tissuecoculture techniquesendothelial cellsmesenchymal stem cellsneovascularizationsmooth muscle

Identifiers

PMID25114097
OpenAlexW2118212786

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.