Evidence map›Paper›PMID 30274093›Full record

ArticleMaterials science & engineering. C, Materials for biological applications2018

Vascular extracellular matrix and fibroblasts-coculture directed differentiation of human mesenchymal stem cells toward smooth muscle-like cells for vascular tissue engineering.

Na Li, Hanna Sanyour, Tyler Remund, Patrick Kelly, Zhongkui Hong

Abstract read
In one paragraph

Article in Materials science & engineering. C, Materials for biological applications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Extracellular Matrix-Based Biomaterials for Cardiovascular Tissue Engineering.Journal of cardiovascular development and disease · 2021
    Review
  7. Biochemical pharmacology · 2021
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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.

Na LiDepartment of Biomedical Engineering, University of South Dakota, SD, United States of America; BioSNTR, Sioux Falls, SD, United States of America.
Hanna SanyourDepartment of Biomedical Engineering, University of South Dakota, SD, United States of America; BioSNTR, Sioux Falls, SD, United States of America.
Tyler RemundSanford Health, Sioux Falls, SD, United States of America.
Patrick KellySanford Health, Sioux Falls, SD, United States of America; School of Medicine, University of South Dakota, SD, United States of America.
Zhongkui HongDepartment of Biomedical Engineering, University of South Dakota, SD, United States of America; BioSNTR, Sioux Falls, SD, United States of America. Electronic address: Zhongkui.Hong@usd.edu.

Funding

American Heart Association-American Stroke Association 15SDG25420001
6 · The paper itself

Abstract

Construction of an artificial vascular graft is widely considered a promising strategy in vascular tissue engineering. However, limited sources of functional vascular smooth muscle cells (VSMCs) remain a major obstacle in vascular tissue engineering. In this study, we innovatively developed an approach to obtain functional VSMCs by onsite differentiating human bone marrow-derived mesenchymal stem cells (MSCs) directed by decellularized extracellular matrix (ECM) and fibroblasts. The resulting cells and ECM-cells constructs were characterized by real time RT-PCR, immunofluorescence staining, cell contractile functions, and migration capacity. Our results showed both ECM and fibroblasts induced MSCs differentiation toward VSMC-like cells with increased transcription of marker genes, upregulated expression of contractile apparatus proteins, and enhanced functional activity of VSMC phenotype. Interestingly, our findings revealed that native ECM and fibroblasts-coculture had a higher potential to promote MSCs differentiation into VSMCs than growth factors cocktail (GFC) supplemented culture, thereby providing a potential source of VSMCs for blood vessel constitution.

Indexed as

Blood Vessel ProsthesisCell DifferentiationTissue EngineeringCoculture TechniquesExtracellular MatrixFibroblastsHumansMesenchymal Stem CellsMyocytes, Smooth MuscleDifferentiationExtracellular matrixFibroblastsGrowth factors cocktailMesenchymal stem cellsSmooth muscle cells

Identifiers

PMID30274093
PMCPMC11264340

What OpenQuestion holds

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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.