Evidence map›Paper›PMID 26346126›Full record

ArticleStem cell research & therapy2015

Small intestinal submucosa-derived extracellular matrix bioscaffold significantly enhances angiogenic factor secretion from human mesenchymal stromal cells.

Xin Lin, Mikella Robinson, Tye Petrie, Veronica Spandler, W Douglas Boyd, Claus Svane Sondergaard

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  11. Article
  12. Review
  13. [Preparation and osteogenic effect study of small intestinal submucosa sponge].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2020
    Article
  14. Article
  15. Vascularization in tissue engineering: fundamentals and state-of-art.Progress in biomedical engineering (Bristol, England) · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Vascular precursor cells in tissue injury repair.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  20. Human barrier models for the in vitro assessment of drug delivery.Drug delivery and translational research · 2017
    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

6 authors at 1 institution in 1 country.

Xin LinDepartment of Surgery, UC Davis Medical Center, Sacramento, CA, USA. xinlin@ucdavis.edu.
Mikella RobinsonDepartment of Surgery, UC Davis Medical Center, Sacramento, CA, USA. mbrobinson@ucdavis.edu.
Tye PetrieDepartment of Surgery, UC Davis Medical Center, Sacramento, CA, USA. tyepetrie@ucdavis.edu.
Veronica SpandlerDepartment of Surgery, UC Davis Medical Center, Sacramento, CA, USA. vgs27@humboldt.edu.
W Douglas BoydDepartment of Surgery, Division of Cardiothoracic Surgery, UC Davis Medical Center, Sacramento, CA, USA. wdboyd@ucdavis.edu.
Claus Svane SondergaardDepartment of Surgery, Division of Cardiothoracic Surgery, UC Davis Medical Center, Sacramento, CA, USA. cssondergaard@ucdavis.edu.
University of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe in vivo therapeutic effect of mesenchymal stromal cells (MSCs) is currently believed to be tightly linked to their paracrine secretion ability. However, insufficient or imprecise cell delivery, low cell survival and retention post-transplant, along with harsh donor site microenvironments, are major barriers to the clinical success of MSC therapies. Here we tested a small intestinal submucosa (SIS)-derived extracellular matrix (ECM) bioscaffold augmented with MSCs, with the hypothesis that they will facilitate the precise delivery of increased numbers of MSCs therefore improving cell viability and retention.

methodsIn this study, we evaluated the secretion of angiogenic factors from three human MSC lines cultured on SIS ECM. We used human antibody array and enzyme-linked immunosorbent assay to measure the level of angiogenic factors released from MSCs when cultured on SIS ECM or regular tissue culture plastic. We tested MSCs cultured for three different time points.

resultsWe found that the SIS ECM culture environment can significantly enhance the release of several angiogenic factors when compared to MSCs cultured on standard tissue culture plastic. Specifically, vascular endothelial growth factor and interleukin-8 secretion was significantly increased at 24, 48 and 72 hours postseeding onto SIS ECM whereas vascular endothelial growth factor release for cells cultured on plastic surface remained the same during these time points. We also observed significant donor to donor variation in cytokine production.

conclusionsThis study demonstrates that MSCs transplanted onto a SIS ECM may greatly increase their therapeutic potential through an increase in pro-angiogenic cytokine release.

Indexed as

Tissue ScaffoldsAngiogenesis Inducing AgentsCells, CulturedCulture Media, ConditionedExtracellular MatrixHumansIntestinal MucosaMesenchymal Stem CellsAngiogenesis Inducing AgentsCulture Media, Conditioned

Identifiers

PMID26346126
PMCPMC4562125
OpenAlexW1784588849

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.