Evidence map›Paper›PMID 29240625›Full record

ArticleASAIO journal (American Society for Artificial Internal Organs : 1992)

Orbital Shear Stress Regulates Differentiation and Barrier Function of Primary Renal Tubular Epithelial Cells.

Nicholas Ferrell, Jin Cheng, Simeng Miao, Shuvo Roy, William H Fissell

Abstract read
In one paragraph

Article in ASAIO journal (American Society for Artificial Internal Organs : 1992). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Making In Vitro Tumor Models Whole Again.Advanced healthcare materials · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
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  15. 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

5 authors.

Nicholas FerrellFrom the Division of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Jin ChengFrom the Division of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Simeng MiaoDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Shuvo RoyDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, California.
William H FissellFrom the Division of Nephrology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Funding

Building an Implantable Artificial KidneyU01EB021214 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FISSELL, WILLIAM H, ROY, SHUVO · 2015 to 2018
$6.0M
Protein Handling By Renal Proximal Tubule Epithelial CellsK01DK092357 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI FERRELL, NICHOLAS · 2012 to 2016
$608k
NIBIB NIH HHS U01 EB021214NIDDK NIH HHS K01 DK092357
6 · The paper itself

Abstract

Primary cells cultured in vitro gradually lose features characteristic of the in vivo phenotype. Culture techniques that help maintain cell-specific phenotype are advantageous for development of tissue engineered and bioartificial organs. Here we evaluated the phenotype of primary human renal tubular epithelial cells subjected to fluid shear stress by culturing the cells on an orbital shaker. Transepithelial electrical resistance (TEER), cell density, and gene and protein expression of proximal tubule-specific functional markers were measured in cells subjected to orbital shear stress. Cells cultured on an orbital shaker had increased TEER, higher cell density, and enhanced tubular epithelial specific gene and protein expression. This is likely due at least in part to the mechanical stress applied to the apical surface of the cells although other factors including increased nutrient and oxygen delivery and improved mixing could also play a role. These results suggest that orbital shaker culture may be a simple approach to augmenting the differentiated phenotype of cultured renal epithelial cells.

Indexed as

AnimalsBioartificial OrgansCell DifferentiationCells, CulturedEpithelial CellsHumansKidney Tubules, ProximalStress, MechanicalTissue Engineering

Identifiers

PMID29240625
PMCPMC5995603

What OpenQuestion holds

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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.