Evidence map›Paper›PMID 27162074›Full record

ArticleBiomaterials2016

Inosculation and perfusion of pre-vascularized tissue patches containing aligned human microvessels after myocardial infarction.

Sonja B Riemenschneider, Donald J Mattia, Jacqueline S Wendel, Jeremy A Schaefer, Lei Ye, Pilar A Guzman, Robert T Tranquillo

Abstract read
In one paragraph

Article in Biomaterials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
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  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Collagen Fibril Orientation Instructs Fibroblast Differentiation Via Cell Contractility.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  13. Bioprinting Technologies and Bioinks for Vascular Model Establishment.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Human Endothelial Colony-Forming Cells.Cold Spring Harbor perspectives in medicine · 2022
    Article
  16. Article
  17. Progress in Bioengineering Strategies for Heart Regenerative Medicine.International journal of molecular sciences · 2022
    Review
  18. Cardiac Tissue Engineering for the Treatment of Myocardial Infarction.Journal of cardiovascular development and disease · 2021
    Review
  19. Engineering fiber anisotropy within natural collagen hydrogels.American journal of physiology. Cell physiology · 2021
    Review
  20. 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 1 institution in 2 countries.

Sonja B RiemenschneiderDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, USA.
Donald J MattiaDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
Jacqueline S WendelDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
Jeremy A SchaeferDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
Lei YeDepartment of Medicine, University of Minnesota, Minneapolis, MN, USA; National Heart Research Institute Singapore, National Heart Centre Singapore, Singapore.
Pilar A GuzmanIntegrative Biology and Physiology Phenotyping Core, University of Minnesota, Minneapolis, MN, USA.
Robert T TranquilloDepartment of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN, USA; Department of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA. Electronic address: tranquillo@umn.edu.
University of Minnesota · US

Funding

TRAINING FOR FUTURE BIOTECHNOLOGY DEVELOPMENTT32GM008347 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SCHMIDT-DANNERT, CLAUDIA · 1990 to 2021
$11.0M
Perfusable and beating engineered myocardium from human progenitor cells based onR01HL108670 · NHLBI · UNIVERSITY OF MINNESOTA · PI TRANQUILLO, ROBERT T · 2011 to 2014
$2.9M
NHLBI NIH HHS R01 HL108670NIGMS NIH HHS T32 GM008347
6 · The paper itself

Abstract

A major goal of tissue engineering is the creation of pre-vascularized tissues that have a high density of organized microvessels that can be rapidly perfused following implantation. This is especially critical for highly metabolic tissues like myocardium, where a thick myocardial engineered tissue would require rapid perfusion within the first several days to survive transplantation. In the present work, tissue patches containing human microvessels that were either randomly oriented or aligned were placed acutely on rat hearts post-infarction and for each case it was determined whether rapid inosculation could occur and perfusion of the patch could be maintained for 6 days in an infarct environment. Patches containing self-assembled microvessels were formed by co-entrapment of human blood outgrowth endothelial cells and human pericytes in fibrin gel. Cell-induced gel contraction was mechanically-constrained resulting in samples with high densities of microvessels that were either randomly oriented (with 420 ± 140 lumens/mm(2)) or uniaxially aligned (with 940 ± 240 lumens/mm(2)) at the time of implantation. These patches were sutured onto the epicardial surface of the hearts of athymic rats following permanent ligation of the left anterior descending artery. In both aligned and randomly oriented microvessel patches, inosculation occurred and perfusion of the transplanted human microvessels was maintained, proving the in vivo vascularization potential of these engineered tissues. No difference was found in the number of human microvessels that were perfused in the randomly oriented (111 ± 75 perfused lumens/mm(2)) and aligned (173 ± 97 perfused lumens/mm(2)) patches. Our results demonstrate that tissue patches containing a high density of either aligned or randomly oriented human pre-formed microvessels achieve rapid perfusion in the myocardial infarct environment - a necessary first-step toward the creation of a thick, perfusable heart patch.

Indexed as

Neovascularization, PhysiologicPerfusionTissue EngineeringAnimalsBlood VesselsCells, CulturedHeart Function TestsHumansMyocardial InfarctionRats, NudeInosculationMicrovascularMyocardial infarctionPerfusionPre-vascularizedTissue engineering

Identifiers

PMID27162074
PMCPMC4891978
OpenAlexW2345010496

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.