Evidence map›Paper›PMID 25965067›Full record

ArticlePloS one2015

In vitro recapitulation of functional microvessels for the study of endothelial shear response, nitric oxide and [Ca2+]i.

Xiang Li, Sulei Xu, Pingnian He, Yuxin Liu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Role of shear stress-induced red blood cell released ATP in atherosclerosis.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Leveraging avidin-biotin interaction to quantify permeability property of microvessels-on-a-chip networks.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Bioprinting in Vascularization StrategiesIranian biomedical journal · 2019
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Advances in on-chip vascularization.Regenerative medicine · 2017
    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

4 authors at 2 institutions in 1 country.

Xiang LiDepartment of Cellular and Molecular Physiology, Penn State University, School of Medicine, Hershey, Pennsylvania, United States of America.
Sulei XuDepartment of Cellular and Molecular Physiology, Penn State University, School of Medicine, Hershey, Pennsylvania, United States of America.
Pingnian HeDepartment of Cellular and Molecular Physiology, Penn State University, School of Medicine, Hershey, Pennsylvania, United States of America.
Yuxin LiuLane Department of Computer Science and Electrical Engineering, West Virginia University, Morgantown, West Virginia, United States of America.
Pennsylvania State University · USWest Virginia University · US

Funding

CELLULAR MODULATION OF MICROVESSEL PERMEABILITY IN VIVOR01HL056237 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HE, PINGNIAN · 2001 to 2013
$3.1M
Nitric Oxide and Microvessel Permeability In VivoR01HL084338 · NHLBI · WEST VIRGINIA UNIVERSITY · PI HE, PINGNIAN · 2007 to 2011
$1.6M
Microparticles and microvascular dysfunction in diabetesR01DK097391 · NIDDK · WEST VIRGINIA UNIVERSITY · PI HE, PINGNIAN · 2013 to 2016
$1.4M
CELLULAR MODULATION OF MICROVESSEL PERMEABILITY IN VIVOR29HL056237 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI HE, PINGNIAN · 1997 to 2001
$121k
NHLBI NIH HHS HL084338NHLBI NIH HHS HL56237NHLBI NIH HHS R01 HL056237NHLBI NIH HHS R01 HL084338NHLBI NIH HHS R29 HL056237NIDDK NIH HHS R01 DK097391
6 · The paper itself

Abstract

Microfluidic technologies enable in vitro studies to closely simulate in vivo microvessel environment with complexity. Such method overcomes certain constrains of the statically cultured endothelial monolayers and enables the cells grow under physiological range of shear flow with geometry similar to microvessels in vivo. However, there are still existing knowledge gaps and lack of convincing evidence to demonstrate and quantify key biological features of the microfluidic microvessels. In this paper, using advanced micromanufacturing and microfluidic technologies, we presented an engineered microvessel model that mimicked the dimensions and network structures of in vivo microvessels with a long-term and continuous perfusion capability, as well as high-resolution and real-time imaging capability. Through direct comparisons with studies conducted in intact microvessels, our results demonstrated that the cultured microvessels formed under perfused conditions recapitulated certain key features of the microvessels in vivo. In particular, primary human umbilical vein endothelial cells were successfully cultured the entire inner surfaces of the microchannel network with well-developed junctions indicated by VE-cadherin staining. The morphological and proliferative responses of endothelial cells to shear stresses were quantified under different flow conditions which was simulated with three-dimensional shear dependent numerical flow model. Furthermore, we successfully measured agonist-induced changes in intracellular Ca2+ concentration and nitric oxide production at individual endothelial cell levels using fluorescence imaging. The results were comparable to those derived from individually perfused intact venules. With in vivo validation of its functionalities, our microfluidic model demonstrates a great potential for biological applications and bridges the gaps between in vitro and in vivo microvascular research.

Indexed as

MicrofluidicsCalciumCell ProliferationHumansHuman Umbilical Vein Endothelial CellsMicrovesselsNitric OxideCalciumNitric Oxide

Identifiers

PMID25965067
PMCPMC4429116
OpenAlexW1535338082

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.