Evidence map›Paper›PMID 19544388›Full record

ArticleJournal of cellular physiology2009

Sustained epidermal growth factor receptor levels and activation by tethered ligand binding enhances osteogenic differentiation of multi-potent marrow stromal cells.

Manu O Platt, Arian J Roman, Alan Wells, Douglas A Lauffenburger, Linda G Griffith

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact, top 96% 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

35 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. Synthetic alternatives to Matrigel.Nature reviews. Materials · 2020
    Article
  4. Article
  5. Article
  6. Biological functions of mesenchymal stem cells and clinical implications.Cellular and molecular life sciences : CMLS · 2019
    Review
  7. Article
  8. Article
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  10. Review
  11. Article
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  15. Review
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  17. Review
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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

5 authors at 2 institutions in 1 country.

Manu O PlattDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Arian J Roman
Alan Wells
Douglas A Lauffenburger
Linda G Griffith
Massachusetts Institute of Technology · USUniversity of Pittsburgh Medical Center · US

Funding

STRUCTUREU54GM064346 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI IMPERIALI, BARBARA · 2001 to 2010
$74.9M
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
BIOENGINEERED POLYMERS FOR PARSING CELL RESPONSESR01GM059870 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRIFFITH, LINDA G · 1999 to 2007
$2.4M
Bioengineering Polymers for Parsing Cell ResponsesR01DE019523 · NIDCR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRIFFITH, LINDA G · 2008 to 2012
$1.7M
NCRR NIH HHS P40 RR017447NCRR NIH HHS P40RR017447NIDCR NIH HHS R01 DE019523NIDCR NIH HHS R01-DE 019523-10NIGMS NIH HHS R01 GM059870NIGMS NIH HHS R01-GM059870-07NIGMS NIH HHS R01 GM069668NIGMS NIH HHS U54 GM064346
6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR)-mediated signaling helps regulate bone development and healing through its effects on osteogenic cells. Here, we show how EGFR activity and osteogenic differentiation responses in primary human bone marrow-derived multipotent stromal cells (MSCs) are influenced by presenting covalently tethered epidermal growth factor (tEGF) on the culture substratum, a presentation mode that reduces EGFR internalization and restricts signaling to the cell surface. In both absence and presence of tEGF, MSCs increase expression levels of EGFR and its heterodimerization partner HER2 during the course of osteogenic differentiation. tEGF substrata increased levels of phosphorylated EGFR and phosphorylated extracellular regulated kinase (ERK) compared to control substrata, and these elevations were associated with a twofold enhancement of MSC alkaline phosphatase activity at day 7 and matrix mineralization at day 21. Surprisingly, addition of soluble EGF (sEGF) to cells cultured on tEGF substrata reduces osteogenic differentiation, even though EGFR signaling is more strongly activated in acute, short-term manner by sEGF treatment than by tEGF treatment. A striking concomitant result of the sEGF effects is near-complete downregulation of EGFR and HER2, demonstrating that the tEGF/EGFR interaction is dynamically reversible even though temporally sustained. Taken together, our results show that enhanced MSC osteogenic differentiation corresponds to a sustained combination of receptor expression and ligand presentation, both of which are maintained by tEGF.

Indexed as

Cell DifferentiationOsteogenesisBone Marrow CellsBone MatrixCalcification, PhysiologicCell Line, TransformedCell ProliferationEnzyme ActivationEpidermal Growth FactorErbB ReceptorsHumansLigandsModels, BiologicalMultipotent Stem CellsPhosphorylationRNA, MessengerEpidermal Growth FactorErbB ReceptorsLigandsRNA, MessengerTransforming Growth Factor alpha

Identifiers

PMID19544388
PMCPMC3084602
OpenAlexW1493223204

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.