Evidence map›Paper›PMID 20808289›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2010

siRNA nanoparticle functionalization of nanostructured scaffolds enables controlled multilineage differentiation of stem cells.

Morten Ø Andersen, Jens V Nygaard, Jorge S Burns, Merete K Raarup, Jens R Nyengaard, Cody Bünger, Flemming Besenbacher, Kenneth A Howard, Moustapha Kassem, Jørgen Kjems

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-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

28 citing papers in PubMed, 80 citations in OpenAlex.

  1. The Role of SOX Transcription Factors in Ageing and Age-Related Diseases.International journal of molecular sciences · 2023
    Review
  2. Identifying Biomarkers for Osteogenic Potency Assay Development.Advances in experimental medicine and biology · 2023
    Article
  3. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Technologies for controlled, local delivery of siRNA.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  15. Multilayered Magnetic Gelatin Membrane Scaffolds.ACS applied materials & interfaces · 2015
    Article
  16. Article
  17. Review
  18. Article
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  20. 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

10 authors at 3 institutions in 2 countries.

Morten Ø AndersenInterdisciplinary Nanoscience Center, Aarhus University, Aarhus C, Denmark.
Jens V Nygaard
Jorge S Burns
Merete K Raarup
Jens R Nyengaard
Cody Bünger
Flemming Besenbacher
Kenneth A Howard
Moustapha Kassem
Jørgen Kjems
Aarhus University · DKKing Saud University · SAOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The creation of complex tissues and organs is the ultimate goal in tissue engineering. Engineered morphogenesis necessitates spatially controlled development of multiple cell types within a scaffold implant. We present a novel method to achieve this by adhering nanoparticles containing different small-interfering RNAs (siRNAs) into nanostructured scaffolds. This allows spatial retention of the RNAs within nanopores until their cellular delivery. The released siRNAs were capable of gene silencing BCL2L2 and TRIB2, in mesenchymal stem cells (MSCs), enhancing osteogenic and adipogenic differentiation, respectively. This approach for enhancing a single type of differentiation is immediately applicable to all areas of tissue engineering. Different nanoparticles localized to spatially distinct locations within a single implant allowed two different tissue types to develop in controllable areas of an implant. As a consequence of this, we predict that complex tissues and organs can be engineered by the in situ development of multiple cell types guided by spatially restricted nanoparticles.

Indexed as

Tissue ScaffoldsAdipocytesAnimalsApoptosisApoptosis Regulatory ProteinsBlotting, WesternCalcium-Calmodulin-Dependent Protein KinasesCell DifferentiationCell ProliferationCells, CulturedChondrogenesisDNA-Activated Protein KinaseDNA-Binding ProteinsFemaleFlow CytometryGene SilencingApoptosis Regulatory ProteinsBCL2L2 protein, humanCalcium-Calmodulin-Dependent Protein KinasesDNA-Activated Protein KinaseDNA-Binding Proteinsenhanced green fluorescent proteinGreen Fluorescent ProteinsIntracellular Signaling Peptides and ProteinsNuclear ProteinsPrkdc protein, mouseRNA, MessengerRNA, Small InterferingTRIB2 protein, human

Identifiers

PMID20808289
PMCPMC2990512
OpenAlexW2081592256

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.