Evidence map›Paper›PMID 27063496›Full record

ArticleActa biomaterialia2016

A tenascin-C mimetic peptide amphiphile nanofiber gel promotes neurite outgrowth and cell migration of neurosphere-derived cells.

Eric J Berns, Zaida Álvarez, Joshua E Goldberger, Job Boekhoven, John A Kessler, H Georg Kuhn, Samuel I Stupp

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Tenascin CNature communications · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Self-Assembling Hydrogel Structures for Neural Tissue Repair.ACS biomaterials science & engineering · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Design of materials with supramolecular polymers.Progress in polymer science · 2020
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

7 authors at 2 institutions in 2 countries.

Eric J BernsDepartment of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA. Electronic address: eric-berns@u.northwestern.edu.
Zaida ÁlvarezSimpson Querrey Institute for BioNanotechnology, Northwestern University, Chicago, IL 60611, USA. Electronic address: zaida.pinto@northwestern.edu.
Joshua E GoldbergerDepartment of Chemistry, Northwestern University, Evanston, IL 60208, USA. Electronic address: goldberger@chemistry.ohio-state.edu.
Job BoekhovenSimpson Querrey Institute for BioNanotechnology, Northwestern University, Chicago, IL 60611, USA. Electronic address: job.boekhoven@northwestern.edu.
John A KesslerDepartment of Neurology, Northwestern University, Chicago, IL 60611, USA. Electronic address: jakessler@northwestern.edu.
H Georg KuhnCenter for Brain Repair and Rehabilitation, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenberg 413 90, Sweden. Electronic address: Georg.Kuhn@neuro.gu.se.
Samuel I StuppDepartment of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA; Simpson Querrey Institute for BioNanotechnology, Northwestern University, Chicago, IL 60611, USA; Department of Chemistry, Northwestern University, Evanston, IL 60208, USA; Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA; Department of Medicine, Northwestern University, Chicago, IL 60611, USA. Electronic address: s-stupp@northwestern.edu.
Northwestern University · USUniversity of Gothenburg · SE

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Regenerative Scaffold Technologies for CNS and DiabetesR01EB003806 · NIBIB · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STUPP, SAMUEL I · 2004 to 2015
$10.7M
Hybrid Nanostructures for Wireless In Vivo Action Potential SensingF32EB007131 · NIBIB · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOLDBERGER, JOSHUA E · 2007 to 2009
$142k
NCI NIH HHS P30 CA060553NIBIB NIH HHS F32 EB007131NIBIB NIH HHS R01 EB003806
6 · The paper itself

Abstract

unlabelledBiomimetic materials that display natural bioactive signals derived from extracellular matrix molecules like laminin and fibronectin hold promise for promoting regeneration of the nervous system. In this work, we investigated a biomimetic peptide amphiphile (PA) presenting a peptide derived from the extracellular glycoprotein tenascin-C, known to promote neurite outgrowth through interaction with β1 integrin. The tenascin-C mimetic PA (TN-C PA) was found to self-assemble into supramolecular nanofibers and was incorporated through co-assembly into PA gels formed by highly aligned nanofibers. TN-C PA content in these gels increased the length and number of neurites produced from neurons differentiated from encapsulated P19 cells. Furthermore, gels containing TN-C PA were found to increase migration of cells out of neurospheres cultured on gel coatings. These bioactive gels could serve as artificial matrix therapies in regions of neuronal loss to guide neural stem cells and promote through biochemical cues neurite extension after differentiation. One example of an important target would be their use as biomaterial therapies in spinal cord injury. STATEMENT OF SIGNIFICANCE: Tenascin-C is an important extracellular matrix molecule in the nervous system and has been shown to play a role in regenerating the spinal cord after injury and guiding neural progenitor cells during brain development, however, minimal research has been reported exploring the use of biomimetic biomaterials of tenascin-C. In this work, we describe a selfassembling biomaterial system in which peptide amphiphiles present a peptide derived from tenascin-C that promotes neurite outgrowth. Encapsulation of neurons in hydrogels of aligned nanofibers formed by tenascin-C-mimetic peptide amphiphiles resulted in enhanced neurite outgrowth. Additionally, these peptide amphiphiles promoted migration of neural progenitor cells cultured on nanofiber coatings. Tenascin-C biomimetic biomaterials such as the one described here have significant potential in neuroregenerative medicine.

Indexed as

AnimalsCell Line, TumorCell MovementCell SurvivalGelsMiceNanofibersNeural Stem CellsNeuritesPeptidesPeptidomimeticsSpheroids, CellularSurface-Active AgentsTenascinGelsPeptidesPeptidomimeticsSurface-Active AgentsTenascinCell migrationNeurite growthPeptide amphiphileSelf assemblyTenascin-C mimetic peptide

Identifiers

PMID27063496
PMCPMC4872638
OpenAlexW2332423789

What OpenQuestion holds

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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.