Evidence map›Paper›PMID 29756533›Full record

ArticleTissue engineering. Part A2018

Genetic Engineering of Mesenchymal Stem Cells for Differential Matrix Deposition on 3D Woven Scaffolds.

Nguyen P T Huynh, Jonathan M Brunger, Catherine C Gloss, Franklin T Moutos, Charles A Gersbach, Farshid Guilak

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  6. Article
  7. Digits in a dish: AnFrontiers in cell and developmental biology · 2023
    Article
  8. A collagen/PLA hybrid scaffold supports tendon-derived cell growth for tendon repair and regeneration.Journal of biomedical materials research. Part B, Applied biomaterials · 2022
    Article
  9. Functional tissue engineering of articular cartilage for biological joint resurfacing-The 2021 Elizabeth Winston Lanier Kappa Delta Award.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Long non-coding RNAeLife · 2020
    Article
  15. Review
  16. 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

6 authors at 4 institutions in 1 country.

Nguyen P T Huynh1 Department of Orthopaedic Surgery, Washington University in Saint Louis , Saint Louis, Missouri.
Jonathan M Brunger4 University of California , San Francisco, San Francisco, California.
Catherine C Gloss1 Department of Orthopaedic Surgery, Washington University in Saint Louis , Saint Louis, Missouri.
Franklin T Moutos5 Cytex Therapeutics, Inc. , Durham, North Carolina.
Charles A Gersbach6 Department of Biomedical Engineering, Duke University , Durham, North Carolina.
Farshid Guilak1 Department of Orthopaedic Surgery, Washington University in Saint Louis , Saint Louis, Missouri.
Shriners Hospitals for Children - St. Louis · USCytex Therapeutics (United States) · USDuke University · USUniversity of California System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue engineering approaches for the repair of osteochondral defects using biomaterial scaffolds and stem cells have remained challenging due to the inherent complexities of inducing cartilage-like matrix and bone-like matrix within the same local environment. Members of the transforming growth factor β (TGFβ) family have been extensively utilized in the engineering of skeletal tissues, but have distinct effects on chondrogenic and osteogenic differentiation of progenitor cells. The goal of this study was to develop a method to direct human bone marrow-derived mesenchymal stem cells (MSCs) to deposit either mineralized matrix or a cartilaginous matrix rich in glycosaminoglycan and type II collagen within the same biochemical environment. This differential induction was performed by culturing cells on engineered three-dimensionally woven poly(ɛ-caprolactone) (PCL) scaffolds in a chondrogenic environment for cartilage-like matrix production while inhibiting TGFβ3 signaling through Mothers against DPP homolog 3 (SMAD3) knockdown, in combination with overexpressing RUNX2, to achieve mineralization. The highest levels of mineral deposition and alkaline phosphatase activity were observed on scaffolds with genetically engineered MSCs and exhibited a synergistic effect in response to SMAD3 knockdown and RUNX2 expression. Meanwhile, unmodified MSCs on PCL scaffolds exhibited accumulation of an extracellular matrix rich in glycosaminoglycan and type II collagen in the same biochemical environment. This ability to derive differential matrix deposition in a single culture condition opens new avenues for developing complex tissue replacements for chondral or osteochondral defects.

Indexed as

AdultCells, CulturedChondrogenesisCollagen Type IICore Binding Factor Alpha 1 SubunitExtracellular MatrixGene Knockdown TechniquesGenetic EngineeringGlycosaminoglycansHumansMesenchymal Stem CellsMineralsOsteogenesisSmad3 ProteinTissue EngineeringTissue ScaffoldsCollagen Type IICore Binding Factor Alpha 1 SubunitGlycosaminoglycansMineralsSmad3 ProteinTransforming Growth Factor beta3cartilagecartilage defectscartilage tissue engineeringregenerative medicine

Identifiers

PMID29756533
PMCPMC6198766
OpenAlexW2802981444

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.