Evidence map›Paper›PMID 23958778›Full record

ArticleActa biomaterialia2013

Micropatterned dermal-epidermal regeneration matrices create functional niches that enhance epidermal morphogenesis.

Amanda L Clement, Thomas J Moutinho, George D Pins

Abstract read
In one paragraph

Article in Acta biomaterialia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Advances in tissue engineering and biofabrication forBioprinting (Amsterdam, Netherlands) · 2023
    Article
  4. Article
  5. Biopolymer Honeycomb Microstructures: A Review.Materials (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Review
  8. Article
  9. Regulatory mechanism of oral mucosal rete peg formation.Journal of molecular histology · 2021
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. A 3D in vitro model of the dermoepidermal junction amenable to mechanical testing.Journal of biomedical materials research. Part A · 2018
    Article
  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

3 authors.

Amanda L ClementBiomedical Engineering Department, Worcester Polytechnic Institute, 100 Institute Road, Worcester, MA 01609, USA; Bioengineering Institute, Worcester Polytechnic Institute, Worcester, MA 01609, USA.
Thomas J Moutinho
George D Pins

Funding

Bio-MicroElectroMechanical Systems Resource CenterP41EB002503 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI TONER, MEHMET · 2004 to 2018
$17.4M
Development of a Composite Cardiac Patch with Synchronized ContractilityR15HL137145 · NHLBI · WORCESTER POLYTECHNIC INSTITUTE · PI PINS, GEORGE D. · 2017 to 2017
$452k
Designing Microfabricated Basal Lamina Analogs to Enhance Skin RegenerationR15EB005645 · NIBIB · WORCESTER POLYTECHNIC INSTITUTE · PI PINS, GEORGE D. · 2007 to 2007
$207k
NHLBI NIH HHS R15 HL137145NIBIB NIH HHS EB-005645NIBIB NIH HHS P41 EB002503NIBIB NIH HHS P41 EB02503NIBIB NIH HHS R15 EB005645
6 · The paper itself

Abstract

Although tissue engineered skin substitutes have demonstrated some clinical success for the treatment of chronic wounds such as diabetic and venous ulcers, persistent graft take and stability remain concerns. Current bilayered skin substitutes lack the characteristic microtopography of the dermal-epidermal junction that gives skin enhanced mechanical stability and creates cellular microniches that differentially promote keratinocyte function to form skin appendages and enhance wound healing. We developed a novel micropatterned dermal-epidermal regeneration matrix (μDERM) which incorporates this complex topography and substantially enhances epidermal morphology. Here, we describe the use of this three-dimensional (3-D) in vitro culture model to systematically evaluate different topographical geometries and to determine their relationship to keratinocyte function. We identified three distinct keratinocyte functional niches: the proliferative niche (narrow geometries), the basement membrane protein synthesis niche (wide geometries) and the putative keratinocyte stem cell niche (narrow geometries and corners). Specifically, epidermal thickness and keratinocyte proliferation is significantly (p<0.05) increased in 50 and 100 μm channels while laminin-332 deposition is significantly (p<0.05) increased in 400 μm channels compared to flat controls. Additionally, β1(bri)p63(+) keratinocytes, putative keratinocyte stem cells, preferentially cluster in channel geometries (similar to clustering observed in native skin) compared to a random distribution on flats. This study identifies specific target geometries to enhance skin regeneration and graft performance. Furthermore, these results suggest the importance of μDERM microtopography in designing the next generation of skin substitutes. Finally, we anticipate that 3-D organotypic cultures on μDERMS will provide a novel tissue engineered skin substitute for in vitro investigations of skin morphogenesis, wound healing and pathology.

Indexed as

MorphogenesisAnimalsBasement MembraneCell ProliferationCells, CulturedCell ShapeDermisEpidermisFibroblastsHumansIntegrin beta1KeratinocytesKi-67 AntigenMaleProtein BiosynthesisRatsIntegrin beta1Ki-67 AntigenTumor Suppressor Proteins3-D organ modelDermal–epidermal junctionKeratinocyte functionMicrotopography

Identifiers

PMID23958778
PMCPMC3818337

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.