Evidence map›Paper›PMID 24225908›Full record

ArticleLab on a chip2014

Microfluidic transwell inserts for generation of tissue culture-friendly gradients in well plates.

Christopher G Sip, Nirveek Bhattacharjee, Albert Folch

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 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
4.5field-weighted citation impact, top 5% 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, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Astrocytes and human artificial blood-brain barrier models.Bosnian journal of basic medical sciences · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Microfluidic devices for neutrophil chemotaxis studies.Journal of translational medicine · 2020
    Review
  13. Modular Microphysiological System for Modeling of Biologic Barrier Function.Frontiers in bioengineering and biotechnology · 2020
    Article
  14. Microfluidics for interrogating live intact tissues.Microsystems & nanoengineering · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

3 authors at 1 institution in 1 country.

Christopher G SipBioengineering, University of Washington, William H. Foege Building, 1705 NE Pacific St. Campus Box 355061, Seattle, Washington, USA. csiprun@uw.edu.
Nirveek Bhattacharjee
Albert Folch
University of Washington · US

Funding

Multiplexed Microfluidic Gradients for Axon GuidanceR01NS064387 · NINDS · UNIVERSITY OF WASHINGTON · PI FOLCH, ALBERT · 2011 to 2015
$1.6M
NINDS NIH HHS R01 NS064387
6 · The paper itself

Abstract

Gradients of biochemical molecules play a key role in many physiological processes such as axon growth, tissue morphogenesis, and trans-epithelium nutrient transport, as well as in pathophysiological phenomena such as wound healing, immune response, bacterial invasion, and cancer metastasis. In this paper, we report a microfluidic transwell insert for generating quantifiable concentration gradients in a user-friendly and modular format that is compatible with conventional cell cultures and with tissue explant cultures. The device is simply inserted into a standard 6-well plate, where it hangs self-supported at a distance of ~250 μm above the cell culture surface. The gradient is created by small microflows from the device, through an integrated track-etched porous membrane, into the cell culture well. The microfluidic transwell can deliver stable, quantifiable gradients over a large area with extremely low fluid shear stress to dissociated cells or tissue explants cultured independently on the surface of a 6-well plate. We used finite-element modeling to describe the porous membrane flow and molecular transport and to predict gradients generated by the device. Using the device, we applied a gradient of the chemotactic peptide N-formyl-met-leu-phe (fMLP) to a large population of HL-60 cells (a neutrophil cell line) and directly observed the migration with time-lapse microscopy. On quantification of the chemotactic response with an automated tracking algorithm, we found 74% of the cells moving towards the gradient. Additionally, the modular design and low fluid shear stress made it possible to apply gradients of growth factors and second messengers to mouse retinal explant cultures. With a simplified interface and well-defined gradients, the microfluidic transwell device has potential for broad applications to gradient-sensing biology.

Indexed as

Microfluidic Analytical TechniquesDimethylpolysiloxanesEquipment DesignFinite Element AnalysisFluorescenceHL-60 CellsHumansTissue Culture TechniquesbaysilonDimethylpolysiloxanes

Identifiers

PMID24225908
PMCPMC4362725
OpenAlexW2136388451

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.