Evidence map›Paper›PMID 21720642›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2011

Harnessing endogenous growth factor activity modulates stem cell behavior.

Gregory A Hudalla, Nicholas A Kouris, Justin T Koepsel, Brenda M Ogle, William L Murphy

Abstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2011. 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
4.0field-weighted citation impact, top 6% 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, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Nanoscale Coatings for Ultralow Dose BMP-2-Driven Regeneration of Critical-Sized Bone Defects.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Tuning cellular responses to BMP-2 with material surfaces.Cytokine & growth factor reviews · 2016
    Review
  15. Article
  16. Design of growth factor sequestering biomaterials.Chemical communications (Cambridge, England) · 2014
    Review
  17. Article
  18. Article
  19. Chitosan-based scaffolds for bone tissue engineering.Journal of materials chemistry. B · 2014
    Article
  20. Materials as stem cell regulators.Nature materials · 2014
    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

5 authors at 3 institutions in 1 country.

Gregory A HudallaDepartment of Biomedical Engineering, University of Wisconsin, 2130 Engineering Centers Building, 1550 Engineering Drive, Madison, WI 53706, USA.
Nicholas A Kouris
Justin T Koepsel
Brenda M Ogle
William L Murphy
In-Q-Tel · USUniversity of Wisconsin–Madison · USHighland Community College - Illinois · US

Funding

Biomaterials for local regulation of growth factor signalingR01HL093282 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MURPHY, WILLIAM L. · 2009 to 2018
$3.3M
Towards a synthetic basement membrane for the corneal epitheliumR01EY017367 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI NEALEY, PAUL F. · 2007 to 2010
$1.4M
NEI NIH HHS R01 EY017367NEI NIH HHS R01EY017367NHLBI NIH HHS R01 HL093282NHLBI NIH HHS R01HL093282
6 · The paper itself

Abstract

The influence of specific serum-borne biomolecules (e.g. heparin) on growth factor-dependent cell behavior is often difficult to elucidate in traditional cell culture due to the random, non-specific nature of biomolecule adsorption from serum. We hypothesized that chemically well-defined cell culture substrates could be used to study the influence of sequestered heparin on human mesenchymal stem cell (hMSC) behavior. Specifically, we used bio-inert self-assembled monolayers (SAMs) chemically modified with a bioinspired heparin-binding peptide (termed "HEPpep") and an integrin-binding peptide (RGDSP) as stem cell culture substrates. Our results demonstrate that purified heparin binds to HEPpep SAMs in a dose-dependent manner, and serum-borne heparin binds specifically and in a dose-dependent manner to HEPpep SAMs. These heparin-sequestering SAMs enhance hMSC proliferation by amplifying endogenous fibroblast growth factor (FGF) signaling, and enhance hMSC osteogenic differentiation by amplifying endogenous bone morphogenetic protein (BMP) signaling. The effects of heparin-sequestering are similar to the effects of supraphysiologic concentrations of recombinant FGF-2. hMSC phenotype is maintained over multiple population doublings on heparin-sequestering substrates in growth medium, while hMSC osteogenic differentiation is enhanced in a bone morphogenetic protein-dependent manner on the same substrates during culture in osteogenic induction medium. Together, these observations demonstrate that the influence of the substrate on stem cell phenotype is sensitive to the culture medium formulation. Our results also demonstrate that enhanced hMSC proliferation can be spatially localized by patterning the location of HEPpep on the substrate. Importantly, the use of chemically well-defined SAMs in this study eliminated the confounding factor of random, non-specific biomolecule adsorption, and identified serum-borne heparin as a key mediator of hMSC response to endogenous growth factors.

Indexed as

AdsorptionBone Morphogenetic ProteinsCell DifferentiationCell ProliferationCulture MediaFibroblast Growth Factor 2HeparinHumansIntercellular Signaling Peptides and ProteinsMesenchymal Stem CellsOsteogenesisPhenotypeProtein BindingRecombinant ProteinsSignal TransductionSurface Plasmon ResonanceBone Morphogenetic ProteinsCulture MediaFibroblast Growth Factor 2HeparinIntercellular Signaling Peptides and ProteinsRecombinant Proteins

Identifiers

PMID21720642
PMCPMC3996706
OpenAlexW1989506277

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.