Evidence map›Paper›PMID 29770525›Full record

ArticleMicrocirculation (New York, N.Y. : 1994)2018

Establishment and characterization of an embryonic pericyte cell line.

Huaning Zhao, Jordan Darden, John C Chappell

Open access · greenAbstract read
In one paragraph

Article in Microcirculation (New York, N.Y. : 1994), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. From Donor to the Lab: A Fascinating Journey of Primary Cell Lines.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Pericytes in Vascular Development.Current tissue microenvironment reports · 2020
    Article
  9. Article
  10. Article
  11. The pericyte microenvironment during vascular development.Microcirculation (New York, N.Y. : 1994) · 2019
    Review
  12. Article
  13. Microvascular bioengineering: a focus on pericytes.Journal of biological engineering · 2019
    Review
  14. [Research Advances of Ang-2 in Non-small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2018
    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

3 authors at 1 institution in 1 country.

Huaning ZhaoCenter for Heart and Regenerative Medicine, Virginia Tech Carilion Research Institute, Roanoke, VA, USA.
Jordan DardenCenter for Heart and Regenerative Medicine, Virginia Tech Carilion Research Institute, Roanoke, VA, USA.
John C ChappellCenter for Heart and Regenerative Medicine, Virginia Tech Carilion Research Institute, Roanoke, VA, USA.ORCID 0000-0002-0427-5170
Carilion Roanoke Memorial Hospital · US

Funding

The Role of Vascular Flt-1 in Endothelial-Pericyte InteractionsR00HL105779 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CHAPPELL, JOHN CHRISTOPHER · 2015 to 2017
$727k
Flt-VEGF-Cx43 Regulation of Vascular Pericyte InvestmentR56HL133826 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CHAPPELL, JOHN CHRISTOPHER · 2016 to 2016
$386k
NHLBI NIH HHS R00 HL105779NHLBI NIH HHS R56 HL133826
6 · The paper itself

Abstract

objectivePericytes are specialized perivascular cells embedded within the basement membrane. These cells envelope the abluminal surface of endothelial cells and promote microvessel homeostasis. Recent discoveries of unique pericyte functions, particularly in neural tissues, underscore the need for overcoming existing challenges in establishing a functionally validated pericyte cell line. Here, we present methodologies for addressing these challenges as well as an embryonic pericyte cell line for use with in vitro and ex vivo experimental models.

methodsWe isolated an enriched population of NG2:DsRed+ pericytes from E12.5 mice. This pericyte cell line was compared to MEFs with respect to gene expression, cell morphology and migration, and engagement with endothelial cells during junction stabilization and angiogenesis.

resultsNG2+ pericytes displayed gene expression patterns, cell morphology, and 2D migration behaviors distinct from MEFs. In three different vessel formation models, pericytes from this line migrated to and incorporated into developing vessels. When co-cultured with HUVECs, these pericytes stimulated more robust VE-Cadherin junctions between HUVECs as compared to MEFs, as well as contributed to HUVEC organization into primitive vascular structures.

conclusionsOur data support use of this pericyte cell line in a broad range of models to further understand pericyte functionality during normal and pathological conditions.

Indexed as

AnimalsBlood VesselsCell LineCell MovementCell SeparationCoculture TechniquesEmbryo, MammalianGene ExpressionHumansMiceMice, Inbred StrainsPericytesendothelial cellsmouse embryonic fibroblastspericytesvascular morphogenesis

Identifiers

PMID29770525
PMCPMC7311072
OpenAlexW2804095409

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.