Evidence map›Paper›PMID 26102992›Full record

ArticleBiomaterials2015

Enhanced therapeutic neovascularization by CD31-expressing cells and embryonic stem cell-derived endothelial cells engineered with chitosan hydrogel containing VEGF-releasing microtubes.

Sangho Lee, Chandra M Valmikinathan, Jaemin Byun, Sangsung Kim, Geehee Lee, Nassir Mokarram, S Balakrishna Pai, Elisa Um, Ravi V Bellamkonda, Young-sup Yoon

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Engineering approaches for cardiac organoid formation and their characterization.Translational research : the journal of laboratory and clinical medicine · 2022
    Review
  17. Preparation of IonMarine drugs · 2022
    Article
  18. Review
  19. Review
  20. 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

10 authors at 3 institutions in 1 country.

Sangho LeeDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Chandra M ValmikinathanWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, 313 Ferst Drive, Atlanta, GA 30332, USA.
Jaemin ByunDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Sangsung KimDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Geehee LeeDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Nassir MokarramWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, 313 Ferst Drive, Atlanta, GA 30332, USA.
S Balakrishna PaiWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, 313 Ferst Drive, Atlanta, GA 30332, USA.
Elisa UmDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA.
Ravi V BellamkondaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, 313 Ferst Drive, Atlanta, GA 30332, USA.
Young-sup YoonDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, 101 Woodruff Circle, Atlanta, GA 30322, USA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, 313 Ferst Drive, Atlanta, GA 30332, USA; Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 120-752, South Korea. Electronic address: yyoon5@emory.edu.
Emory University · USGeorgia Institute of Technology · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Cell therapy for diabetic peripheral neurovascular complicationsDP3DK094346 · NIDDK · EMORY UNIVERSITY · PI CHENG, XIAODONG, YOON, YOUNG-SUP · 2011 to 2011
$6.1M
Effects of reprogrammed and engineered MSCs on diabetic complicationsDP3DK108245 · NIDDK · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2015 to 2016
$2.6M
Stem Cell-based therapy for LymphedemaR01HL127759 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2015 to 2018
$1.6M
Cardiac Regeneration with Bioengineered Human Stem CellsR01HL129511 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2016 to 2019
$1.6M
NHLBI NIH HHS HHSN268201000043CNHLBI NIH HHS R01 HL127759NHLBI NIH HHS R01 HL129511NIDDK NIH HHS DP3 DK094346NIDDK NIH HHS DP3DK094346NIDDK NIH HHS DP3 DK108245
6 · The paper itself

Abstract

Various stem cells and their progeny have been used therapeutically for vascular regeneration. One of the major hurdles for cell-based therapy is low cell retention in vivo, and to improve cell survival several biomaterials have been used to encapsulate cells before transplantation. Vascular regeneration involves new blood vessel formation which consists of two processes, vasculogenesis and angiogenesis. While embryonic stem cell (ESC)-derived endothelial cells (ESC-ECs) have clearer vasculogenic potency, adult cells exert their effects mainly through paracrine angiogenic activities. While these two cells have seemingly complementary advantages, there have not been any studies to date combining these two cell types for vascular regeneration. We have developed a novel chitosan-based hydrogel construct that encapsulates both CD31-expressing BM-mononuclear cells (BM-CD31(+) cells) and ESC-ECs, and is loaded with VEGF-releasing microtubes. This cell construct showed high cell survival and minimal cytotoxicity in vitro. When implanted into a mouse model of hindlimb ischemia, it induced robust cell retention, neovascularization through vasculogenesis and angiogenesis, and efficiently induced recovery of blood flow in ischemic hindlimbs. This chitosan-based hydrogel encapsulating mixed adult and embryonic cell derivatives and containing VEGF can serve as a novel platform for treating various cardiovascular diseases.

Indexed as

AnimalsCells, CulturedChitosanEmbryonic Stem CellsEndothelial CellsHindlimbHydrogel, Polyethylene Glycol DimethacrylateIschemiaMaleMiceNeovascularization, PhysiologicPlatelet Endothelial Cell Adhesion Molecule-1Tissue ScaffoldsVascular Endothelial Growth Factor AChitosanHydrogel, Polyethylene Glycol DimethacrylatePlatelet Endothelial Cell Adhesion Molecule-1Vascular Endothelial Growth Factor ACD31(+) cellsChitosan hydrogelEmbryonic stem cellsLipid microtubesVascular regeneration

Identifiers

PMID26102992
PMCPMC4489430
OpenAlexW639515221

What OpenQuestion holds

Textmetadata
LicenceTDM
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.