Evidence map›Paper›PMID 18564029›Full record

ArticleStem cells and development2008

Differentiation of bone marrow mesenchymal stem cells into the smooth muscle lineage by blocking ERK/MAPK signaling pathway.

Kenichi Tamama, Chandan K Sen, Alan Wells

Open access · greenAbstract read
In one paragraph

Article in Stem cells and development, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Identification of CD141Stem cell research & therapy · 2024
    Article
  5. Bioengineering of Intestinal Grafts.Gastroenterology clinics of North America · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Response of vascular mesenchymal stem/progenitor cells to hyperlipidemia.Cellular and molecular life sciences : CMLS · 2018
    Review
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.

Kenichi TamamaDepartment of Pathology, Ohio State University Medical Center, Columbus, Ohio 43210, USA. kenichi.tamama@osumc.edu
Chandan K Sen
Alan Wells
University of Pittsburgh · US

Funding

PREPARATION AND DISTRUBUTION OF ADULT STEM CELLS: HUMAN &RODENTP40RR017447 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI PROCKOP, DARWIN JOHNSON · 2003 to 2011
$8.9M
Spatial Segregation of Cell Functioning During MotilityR01GM069668 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2004 to 2019
$4.7M
Dermal-Epidermal Communication during Wound HealingR01GM063569 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2003 to 2018
$3.7M
Redox Control of Wound HealingR01GM069589 · NIGMS · OHIO STATE UNIVERSITY · PI SEN, CHANDAN K · 2004 to 2013
$2.3M
Tissue Oxygenation and Wound HealingR01GM077185 · NIGMS · OHIO STATE UNIVERSITY · PI SEN, CHANDAN K · 2007 to 2016
$2.3M
Oxygen Sensitive Signaling in Primary Cardiac FibroblastR01HL073087 · NHLBI · OHIO STATE UNIVERSITY · PI SEN, CHANDAN K · 2004 to 2007
$1.3M
NCRR NIH HHS P40RR017447NHLBI NIH HHS R01 HL073087NHLBI NIH HHS R01HL073087NIGMS NIH HHS R01 GM063569NIGMS NIH HHS R01GM063569NIGMS NIH HHS R01 GM069589NIGMS NIH HHS R01GM 069589NIGMS NIH HHS R01 GM069668NIGMS NIH HHS R01 GM077185NIGMS NIH HHS R01GM 077185
6 · The paper itself

Abstract

Smooth muscle cells (SMCs) are major components of blood vessels and other hollow visceral organs required for tissue engineering of these organs. This study aims to evaluate whether adult bone marrow-derived mesenchymal stem cells (BMMSCs), multipotent cells, can be converted into SMCs. We examined the ERK/MAPK pathway as it exerts anti-myogenic signals in SMCs. Undifferentiated BMMSCs express most SMC marker genes, albeit mainly at low levels, except smooth muscle myosin heavy chain (SMMHC), the most definitive marker of differentiated SMC. The treatment of BMMSC with MEK inhibitor up-regulated the expression of alpha-smooth muscle actin (ASMA), h-caldesmon, and SMMHC in BMMSC in low serum condition. MEK inhibitor-treated BMMSC also contracted a collagen gel in response to endothelin. Interestingly, inhibition of MEK induced myocardin expression in BMMSC. In conclusion, BMMSCs treated MEK inhibitor gain a SMC-like phenotype with ligand-induced cell contractility to endothelin in vitro. This approach has obvious implications for cell therapeutics and tissue engineering of hollow visceral organs such as blood vessels.

Indexed as

Cell DifferentiationCell LineageMAP Kinase Signaling SystemActinsBecaplerminBone Marrow CellsCalmodulin-Binding ProteinsCells, CulturedCollagenEndothelinsets-Domain Protein Elk-1Extracellular Signal-Regulated MAP KinasesGap JunctionsGelsGene Expression RegulationHumansActinsBecaplerminCalmodulin-Binding ProteinsCollagenELK1 protein, humanEndothelinsets-Domain Protein Elk-1Extracellular Signal-Regulated MAP KinasesGelsMicrofilament ProteinsMuscle ProteinsMyocardinMyosin Heavy ChainsNuclear ProteinsPlatelet-Derived Growth FactorProtein Kinase InhibitorsProto-Oncogene Proteins c-sisRNA, MessengerTrans-ActivatorsTranscription Factorstransgelin

Identifiers

PMID18564029
PMCPMC2973839
OpenAlexW2072949048

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.