Evidence map›Paper›PMID 33247781›Full record

ArticleJournal of materials science. Materials in medicine2020

Endothelial progenitor/stem cells in engineered vessels for vascular transplantation.

Durai Murugan Muniswami, L Vinod Kumar Reddy, Soosai Manickam Amirtham, Sandhya Babu, Arunai Nambi Raj, Dwaipayan Sen, Geetha Manivasagam

Abstract read
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In one paragraph

Article in Journal of materials science. Materials in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. The journey of decellularized vessel: from laboratory to operating room.Frontiers in bioengineering and biotechnology · 2024
    Review
  4. Article
  5. Review
  6. 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

7 authors at 2 institutions in 1 country.

Durai Murugan MuniswamiCentre for Biomaterials, Cellular & Molecular Theranostics (CBCMT), VIT, Vellore, India. durai.morgan@gmail.com.ORCID http://orcid.org/0000-0001-6838-9727
L Vinod Kumar ReddyCentre for Biomaterials, Cellular & Molecular Theranostics (CBCMT), VIT, Vellore, India.
Soosai Manickam AmirthamDepartment of Physiology, Christian Medical College, Vellore, 632002, India.
Sandhya BabuSandhya Hospital, Vellore, 632009, India.
Arunai Nambi RajCentre for Biomaterials, Cellular & Molecular Theranostics (CBCMT), VIT, Vellore, India.
Dwaipayan SenCentre for Biomaterials, Cellular & Molecular Theranostics (CBCMT), VIT, Vellore, India.
Geetha ManivasagamCentre for Biomaterials, Cellular & Molecular Theranostics (CBCMT), VIT, Vellore, India.
Christian Medical College, Vellore · INKarpagam Academy of Higher Education · IN

Funding

Science and Engineering Research Board PDF/2016/003643
6 · The paper itself

Abstract

backgroundDysfunction of blood vessel leads to aneurysms, myocardial infarction and other thrombosis conditions. Current treatment strategies are transplantation of blood vessels from one part of the body to other dysfunction area, or allogenic, synthetic. Due to shortage of the donor, painful dissection, and lack of efficacy in synthetic, there is a need for alternative to native blood vessels for transplantation.

methodsHuman umbilical-cord tissue obtained from the hospital with the informed consent. Umbilical-cord blood vessels were isolated for decellularization and to establish endothelial cell culture. Cultured cells were characterized by immunophenotype, gene expression and in vitro angiogenesis assay. Decellularized blood vessels were recellularized with the endothelial progenitors and Wharton jelly, CL MSCs (1:1), which was characterized by MTT, biomechanical testing, DNA content, SEM and histologically. Bioengineered vessels were transplanted into the animal models to evaluate their effect.

resultsCultured cells express CD31 and CD14 determining endothelial progenitor cells (EPCs). EPCs expresses various factors such as angiopoitin1, VWF, RANTES, VEGF, BDNF, FGF1, FGF2, HGF, IGF, GDNF, NGF, PLGF, NT3, but fail to express NT4, EGF, and CNTF. Pro and anti-inflammatory cytokine expressions were noticed. Functionally, these EPCs elicit in vitro tube formation. Negligible DNA content and intact ECM confirms the efficient decellularization of tissue. The increased MTT activity in recellularized tissue determines proliferating cells and biocompatibility of the scaffolds. Moreover, significant (P < 0.05) increase in maximum force and tensile of recellularized biomaterial as compared to the decellularized scaffolds. Integration of graft with host tissue, suggesting biocompatible therapeutic biomaterial with cells.

conclusionEPCs with stem cells in engineered blood vessels could be therapeutically applicable in vascular surgery.

Indexed as

Blood Vessel ProsthesisAnimalsBiomechanical PhenomenaCell Culture TechniquesCells, CulturedCord Blood Stem Cell TransplantationEndothelial Progenitor CellsHumansMaterials TestingMesenchymal Stem CellsRatsRats, Wistar

Identifiers

PMID33247781
OpenAlexW3108387665

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.