Evidence map›Paper›PMID 25857666›Full record

ArticleLab on a chip2015

Multi-cellular 3D human primary liver cell culture elevates metabolic activity under fluidic flow.

Mandy B Esch, Jean-Matthieu Prot, Ying I Wang, Paula Miller, Jose Ricardo Llamas-Vidales, Brian A Naughton, Dawn R Applegate, Michael L Shuler

Abstract read
In one paragraph

Article in Lab on a chip, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 166 citations in OpenAlex.

  1. Article
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  11. Organ-on-a-Chip:Pharmaceutics · 2024
    Article
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  13. Article
  14. Review
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  19. Microtechnology-basedAPL bioengineering · 2021
    Review
  20. Review

12 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 1 country.

Mandy B EschDepartment of Biomedical Engineering, 305 Weill Hall, Cornell University, Ithaca, NY 853, USA. mls50@cornell.edu.
Jean-Matthieu Prot
Ying I Wang
Paula Miller
Jose Ricardo Llamas-Vidales
Brian A Naughton
Dawn R Applegate
Michael L Shuler
Ithaca College · USRegeneMed (United States) · USCornell University · US

Funding

Microphysiologial systems and low cost microfluidic platform with analyticsUH2TR000516 · NCATS · CORNELL UNIVERSITY · PI HICKMAN, JAMES J, SHULER, MICHAEL L · 2012 to 2014
$2.9M
NCATS NIH HHS UH2 TR000516NCATS NIH HHS UH2 TR000516-01
6 · The paper itself

Abstract

We have developed a low-cost liver cell culture device that creates fluidic flow over a 3D primary liver cell culture that consists of multiple liver cell types, including hepatocytes and non-parenchymal cells (fibroblasts, stellate cells, and Kupffer cells). We tested the performance of the cell culture under fluidic flow for 14 days, finding that hepatocytes produced albumin and urea at elevated levels compared to static cultures. Hepatocytes also responded with induction of P450 (CYP1A1 and CYP3A4) enzyme activity when challenged with P450 inducers, although we did not find significant differences between static and fluidic cultures. Non-parenchymal cells were similarly responsive, producing interleukin 8 (IL-8) when challenged with 10 μM bacterial lipoprotein (LPS). To create the fluidic flow in an inexpensive manner, we used a rocking platform that tilts the cell culture devices at angles between ±12°, resulting in a periodically changing hydrostatic pressure drop between reservoirs and the accompanying periodically changing fluidic flow (average flow rate of 650 μL min(-1), and a maximum shear stress of 0.64 dyne cm(-2)). The increase in metabolic activity is consistent with the hypothesis that, similar to unidirectional fluidic flow, primary liver cell cultures increase their metabolic activity in response to fluidic flow periodically changes direction. Since fluidic flow that changes direction periodically drastically changes the behavior of other cells types that are shear sensitive, our findings support the theory that the increase in hepatic metabolic activity associated with fluidic flow is either activated by mechanisms other than shear sensing (for example increased opportunities for gas and metabolite exchange), or that it follows a shear sensing mechanism that does not depend on the direction of shear. Our mode of device operation allows us to evaluate drugs under fluidic cell culture conditions and at low device manufacturing and operation costs.

Indexed as

Lab-On-A-Chip DevicesCells, CulturedCytochrome P-450 CYP1A1Cytochrome P-450 CYP3AHepatocytesHumansInterleukin-8LipopolysaccharidesLiverPrimary Cell CultureCXCL8 protein, humanCYP1A1 protein, humanCYP3A4 protein, humanCytochrome P-450 CYP1A1Cytochrome P-450 CYP3AInterleukin-8Lipopolysaccharides

Identifiers

PMID25857666
PMCPMC4422761
OpenAlexW2172247815

What OpenQuestion holds

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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.