Evidence map›Paper›PMID 22846851›Full record

ArticleMicroscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada2012

On-chip open microfluidic devices for chemotaxis studies.

Gus A Wright, Lino Costa, Alexander Terekhov, Dawit Jowhar, William Hofmeister, Christopher Janetopoulos

Abstract readEvaluation Study
In one paragraph

Article in Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Studying Electrotaxis in Microfluidic Devices.Sensors (Basel, Switzerland) · 2017
    Review
  3. Article
  4. A Customizable Chamber for Measuring Cell Migration.Journal of visualized experiments : JoVE · 2017
    Article
  5. Article
  6. Article
  7. A microfluidic-enabled mechanical microcompressor for the immobilization of live single- and multi-cellular specimens.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2014
    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

6 authors at 2 institutions in 1 country.

Gus A WrightDepartment of Biological Sciences, Vanderbilt University, Nashville, TN 37232, USA.
Lino Costa
Alexander Terekhov
Dawit Jowhar
William Hofmeister
Christopher Janetopoulos
University of Tennessee at Knoxville · USVanderbilt University · US

Funding

PI(3,4,5)P3 Regulates Cell Polarity During Chemotaxis and CytokinesisR01GM080370 · NIGMS · VANDERBILT UNIVERSITY · PI JANETOPOULOS, CHRISTOPHER J · 2008 to 2012
$1.4M
An open microfluidic device to study chemotaxis of eukaryotic cellsF31GM095282 · NIGMS · VANDERBILT UNIVERSITY · PI JOWHAR, DAWIT · 2011 to 2012
$51k
NIGMS NIH HHS 1 F31 GM095282-01A1NIGMS NIH HHS F31 GM095282NIGMS NIH HHS GM080370NIGMS NIH HHS R01 GM080370
6 · The paper itself

Abstract

Microfluidic devices can provide unique control over both the chemoattractant gradient and the migration environment of the cells. Our work incorporates laser-machined micro and nanofluidic channels into bulk fused silica and cover slip-sized silica wafers. We have designed “open” chemotaxis devices that produce passive chemoattractant gradients without an external micropipette system. Since the migration area is unobstructed, cells can be easily loaded and strategically placed into the devices with a standard micropipette. The reusable monolithic glass devices have integral ports that can generate multiple gradients in a single experiment. We also used cover slip microfluidics for chemotaxis assays. Passive gradients elicited from these cover slips could be readily adapted for high throughput chemotaxis assays.We have also demonstrated for the first time that cells can be recruited into cover slip ports eliciting passive chemoattractant gradients. This proves, in principle, that intravital cover slip configurations could deliver controlled amounts of drugs, chemicals, or pathogens as well as recruit cells for proteomic or histological analysis in living animals while under microscopic observation. Intravital cover slip fluidics will create a new paradigm for in vivo observation of biological processes.

Indexed as

ChemotaxisCell MovementCyclic AMPDictyosteliumMicrofluidic Analytical TechniquesMicroscopy, VideoCyclic AMP

Identifiers

PMID22846851
PMCPMC3995343
OpenAlexW2031456554

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.