Evidence map›Paper›PMID 26122935›Full record

ArticleMicrovascular research2015

Human platelet lysate improves human cord blood derived ECFC survival and vasculogenesis in three dimensional (3D) collagen matrices.

Hyojin Kim, Nutan Prasain, Sasidhar Vemula, Michael J Ferkowicz, Momoko Yoshimoto, Sherry L Voytik-Harbin, Mervin C Yoder

Open access · greenAbstract read
In one paragraph

Article in Microvascular research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Article
  4. Human Endothelial Colony-Forming Cells.Cold Spring Harbor perspectives in medicine · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Cord Blood Platelet Lysate: In Vitro Evaluation to Support the Use in Regenerative Medicine.Mediterranean journal of hematology and infectious diseases · 2019
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. 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

7 authors at 2 institutions in 1 country.

Hyojin KimDepartment of Pediatrics, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: kimhyo@iu.edu.
Nutan PrasainDepartment of Pediatrics, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: nprasain@iu.edu.
Sasidhar VemulaDivision of Hematology and Oncology, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: svemula@iu.edu.
Michael J FerkowiczDepartment of Pediatrics, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: mferkow@iu.edu.
Momoko YoshimotoDepartment of Pediatrics, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: myoshimo@iu.edu.
Sherry L Voytik-HarbinWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Drive, West Lafayette, IN 47907, USA. Electronic address: harbins@purdue.edu.
Mervin C YoderDepartment of Pediatrics, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA. Electronic address: myoder@iu.edu.
Indiana University School of MedicinePurdue University West Lafayette · US

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
Collagen Cross-links Direct Matrix-Induced Vasculogenesis Via Tunable PathwaysR01HL109602 · NHLBI · PURDUE UNIVERSITY · PI VOYTIK-HARBIN, SHERRY L, YODER, MERVIN C. · 2011 to 2014
$1.5M
NHLBI NIH HHS HL109602NHLBI NIH HHS R01 HL109602NIDDK NIH HHS P30 DK097512
6 · The paper itself

Abstract

Human cord blood (CB) is enriched in circulating endothelial colony forming cells (ECFCs) that display high proliferative potential and in vivo vessel forming ability. Since diminished ECFC survival is known to dampen the vasculogenic response in vivo, we tested how long implanted ECFC survive and generate vessels in three-dimensional (3D) type I collagen matrices in vitro and in vivo. We hypothesized that human platelet lysate (HPL) would promote cell survival and enhance vasculogenesis in the 3D collagen matrices. We report that the percentage of ECFC co-cultured with HPL that were alive was significantly enhanced on days 1 and 3 post-matrix formation, compared to ECFC alone containing matrices. Also, co-culture of ECFC with HPL displayed significantly more vasculogenic activity compared to ECFC alone and expressed significantly more pro-survival molecules (pAkt, p-Bad and Bcl-xL) in the 3D collagen matrices in vitro. Treatment with Akt1 inhibitor (A-674563), Akt2 inhibitor (CCT128930) and Bcl-xL inhibitor (ABT-263/Navitoclax) significantly decreased the cell survival and vasculogenesis of ECFC co-cultured with or without HPL and implicated activation of the Akt1 pathway as the critical mediator of the HPL effect on ECFC in vitro. A significantly greater average vessel number and total vascular area of human CD31(+) vessels were present in implants containing ECFC and HPL, compared to the ECFC alone implants in vivo. We conclude that implantation of ECFC with HPL in vivo promotes vasculogenesis and augments blood vessel formation via diminishing apoptosis of the implanted ECFC.

Indexed as

Cord Blood Stem Cell TransplantationAnimalsApoptosisBlood PlateletsCells, CulturedCell SurvivalCoculture TechniquesCollagenEndothelial CellsFetal BloodHumansMiceMice, Inbred NODMice, SCIDNeovascularization, PhysiologicPlatelet Endothelial Cell Adhesion Molecule-1AKT1 protein, humanCollagenPlatelet Endothelial Cell Adhesion Molecule-1Proto-Oncogene Proteins c-aktApoptosisEndothelial colony forming cells (ECFCs)Human platelet lysate (HPL)Three dimensional (3D) collagen matrixVasculogenesis

Identifiers

PMID26122935
PMCPMC4537830
OpenAlexW1180301395

What OpenQuestion holds

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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.