Evidence map›Paper›PMID 17099777›Full record

ArticleThe Journal of clinical investigation2006

Cytokine-induced differentiation of multipotent adult progenitor cells into functional smooth muscle cells.

Jeffrey J Ross, Zhigang Hong, Ben Willenbring, Lepeng Zeng, Brett Isenberg, Eu Han Lee, Morayma Reyes, Susan A Keirstead, E Kenneth Weir, Robert T Tranquillo and 1 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

68 citing papers in PubMed, 176 citations in OpenAlex.

  1. Trial
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  15. Review
  16. Review
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  18. Review
  19. Vascular precursor cells in tissue injury repair.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  20. Efficient Differentiation of TBX18Stem cells and development · 2017
    Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Jeffrey J RossStem Cell Institute, University of Minnesota Medical School, Minneapolis, MN, USA.
Zhigang Hong
Ben Willenbring
Lepeng Zeng
Brett Isenberg
Eu Han Lee
Morayma Reyes
Susan A Keirstead
E Kenneth Weir
Robert T Tranquillo
Catherine M Verfaillie
University of Minnesota · USUniversity of Minnesota Medical Center · USKU Leuven · BE

Funding

Opposing Modulation of K+ Channels by a Redox SensorR01HL065322 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WEIR, EDWARD KENNETH · 2001 to 2008
$1.8M
Multipotent Stem Cells in Post Natal Bone MarrowR01DK058295 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI VERFAILLIE, CATHERINE M · 2002 to 2006
$1.5M
DEVELOPMENT OF A BIOARTIFICIAL ARTERYR01HL060495 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI TRANQUILLO, ROBERT T · 1999 to 2002
$888k
NHLBI NIH HHS R01 HL065322NHLBI NIH HHS R01 HL60495NHLBI NIH HHS R01 HL65322NIDDK NIH HHS R01 DK058295NIDDK NIH HHS R01 DK-58295
6 · The paper itself

Abstract

Smooth muscle formation and function are critical in development and postnatal life. Hence, studies aimed at better understanding SMC differentiation are of great importance. Here, we report that multipotent adult progenitor cells (MAPCs) isolated from rat, murine, porcine, and human bone marrow demonstrate the potential to differentiate into cells with an SMC-like phenotype and function. TGF-beta1 alone or combined with PDGF-BB in serum-free medium induces a temporally correct expression of transcripts and proteins consistent with smooth muscle development. Furthermore, SMCs derived from MAPCs (MAPC-SMCs) demonstrated functional L-type calcium channels. MAPC-SMCs entrapped in fibrin vascular molds became circumferentially aligned and generated force in response to KCl, the L-type channel opener FPL64176, or the SMC agonists 5-HT and ET-1, and exhibited complete relaxation in response to the Rho-kinase inhibitor Y-27632. Cyclic distention (5% circumferential strain) for 3 weeks increased responses by 2- to 3-fold, consistent with what occurred in neonatal SMCs. These results provide evidence that MAPC-SMCs are phenotypically and functionally similar to neonatal SMCs and that the in vitro MAPC-SMC differentiation system may be an ideal model for the study of SMC development. Moreover, MAPC-SMCs may lend themselves to tissue engineering applications.

Indexed as

AnimalsAnimals, NewbornBecaplerminCalcium Channel AgonistsCalcium Channels, L-TypeCell DifferentiationCells, CulturedCytokinesFibrinFlow CytometryGene ExpressionHumansMiceMice, Inbred C57BLMultipotent Stem CellsMyocytes, Smooth MuscleBecaplerminCalcium Channel AgonistsCalcium Channels, L-TypeCytokinesFibrinFPL 64176Platelet-Derived Growth FactorProto-Oncogene Proteins c-sisPyrrolesTranscription FactorsTransforming Growth Factor beta

Identifiers

PMID17099777
PMCPMC1635164
OpenAlexW2060952558

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.