Evidence map›Paper›PMID 24593148›Full record

ArticleTissue engineering. Part A2014

Implanted cell-dense prevascularized tissues develop functional vasculature that supports reoxygenation after thrombosis.

Sean M White, Chelsea R Pittman, Ryan Hingorani, Rajan Arora, Tatiana V Esipova, Sergei A Vinogradov, Christopher C W Hughes, Bernard Choi, Steven C George

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 17% 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, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Development of fibroblast/endothelial cell-seeded collagen scaffolds for in vitro prevascularization.Journal of biomedical materials research. Part B, Applied biomaterials · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mature vessel networks in engineered tissue promote graft-host anastomosis and prevent graft thrombosis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Review
  17. Review
  18. Article
  19. Tissue Engineering the Vascular Tree.Tissue engineering. Part B, Reviews · 2017
    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

9 authors at 3 institutions in 1 country.

Sean M White1 Department of Biomedical Engineering, University of California , Irvine, Irvine, California.
Chelsea R Pittman
Ryan Hingorani
Rajan Arora
Tatiana V Esipova
Sergei A Vinogradov
Christopher C W Hughes
Bernard Choi
Steven C George
Beckman Laser Institute and Medical Clinic · USUniversity of California, Irvine · USUniversity of Pennsylvania · US

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
Institute for Clinical and Translational ScienceUL1TR000153 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$12.1M
Virtual Photonocs TechnologiesP41EB015890 · NIBIB · UNIVERSITY OF CALIFORNIA-IRVINE · PI VENUGOPALAN, VASAN · 2012 to 2017
$7.0M
Novel Optical Treatment Approach for Vascular BirthmarksR01HD065536 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI CHOI, BERNARD, KELLY, KRISTEN M · 2010 to 2014
$1.4M
Creating a prevascularized thick implantable human tissueR21HL104203 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GEORGE, STEVEN CARL, HUGHES, CHRISTOPHER C. W. · 2010 to 2011
$421k
NCATS NIH HHS UL1 TR000153NCI NIH HHS P30 CA062203NHLBI NIH HHS R21 HL104203NIBIB NIH HHS P41 EB015890NICHD NIH HHS R01 HD065536PHS HHS P30A062203
6 · The paper itself

Abstract

Achieving adequate vascularization within implanted engineered tissues is a significant obstacle to maintaining viability and functionality. In vitro prevascularization of engineered tissues has been explored as a potential solution to this challenge. The traditional paradigm of in vitro prevascularization is to implant an engineered tissue with a preformed vascular network that is perfused after anastomosis with the host circulation. We investigated the efficacy of this strategy by implanting cell-dense prevascularized tissues created via cell-mediated contraction and composed of collagen and a collagen-fibrin mixture into dorsal window chambers surgically prepared on immunocompromised mice. We found that host-implant anastomosis takes place in 2-6 days and that perfusion of vessels within the implants is subsequently restricted by thrombosis. However, by day 7, a functional vascular network composed of host and implant vessels developed. Prevascularization enhanced intra-implant pO2 significantly as early as 2 days postimplantation, reaching a maximum of 55 mmHg by day 8, which was significantly greater than the maximum within cellularized control tissues (18 mmHg). By day 14, collagen tissues supported ∼ 0.51 × 10(9) implanted and host-derived cells per mL. Our findings elucidate key features of in vitro prevascularization that can be used toward the design of larger and more functionally complex engineered tissues.

Indexed as

AnimalsBlood VesselsCell CountCells, CulturedComposite Tissue AllograftsEndothelial CellsEquipment DesignEquipment Failure AnalysisMiceMice, Inbred ICRMice, SCIDNeovascularization, PhysiologicOxygenThrombosisTissue EngineeringOxygen

Identifiers

PMID24593148
PMCPMC4161156
OpenAlexW2318866146

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.