Evidence map›Paper›PMID 31558920›Full record

ArticleBiomicrofluidics2019

An automated microfluidic device for time-lapse imaging of mouse embryonic stem cells.

Adam F Laing, Venkat Tirumala, Evan Hegarty, Sudip Mondal, Peisen Zhao, William B Hamilton, Joshua M Brickman, Adela Ben-Yakar

Abstract read
In one paragraph

Article in Biomicrofluidics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Adam F LaingDepartment of Mechanical Engineering, The University of Texas at Austin, 204 E. Dean Keeton St., Austin, Texas 78712, USA.
Venkat TirumalaDepartment of Chemical Engineering, The University of Texas at Austin, 200 E. Dean Keeton St., Austin, Texas 78712, USA.
Evan HegartyDepartment of Mechanical Engineering, The University of Texas at Austin, 204 E. Dean Keeton St., Austin, Texas 78712, USA.
Sudip MondalDepartment of Mechanical Engineering, The University of Texas at Austin, 204 E. Dean Keeton St., Austin, Texas 78712, USA.ORCID 0000-0002-5387-0064
Peisen ZhaoDepartment of Electrical and Computer Engineering, The University of Texas at Austin, 2501 Speedway, Austin, Texas 78712, USA.
William B HamiltonThe Novo Nordisk Foundation Center for Stem Cell Biology-DanStem, University of Copenhagen, 3B Blegdamsvej, DK-2200 Copenhagen N, Denmark.
Joshua M BrickmanThe Novo Nordisk Foundation Center for Stem Cell Biology-DanStem, University of Copenhagen, 3B Blegdamsvej, DK-2200 Copenhagen N, Denmark.

Funding

High-speed opto-fluidics to screen entire nervous system in aging and diseaseR01AG041135 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI BEN-YAKAR, ADELA, PIERCE, JONATHAN THOMAS · 2011 to 2015
$2.8M
NIA NIH HHS R01 AG041135
6 · The paper itself

Abstract

Long-term, time-lapse imaging studies of embryonic stem cells (ESCs) require a controlled and stable culturing environment for high-resolution imaging. Microfluidics is well-suited for such studies, especially when the media composition needs to be rapidly and accurately altered without disrupting the imaging. Current studies in plates, which can only add molecules at the start of an experiment without any information on the levels of endogenous signaling before the exposure, are incompatible with continuous high-resolution imaging and cell-tracking. Here, we present a custom designed, fully automated microfluidic chip to overcome these challenges. A unique feature of our chip includes three-dimensional ports that can connect completely sealed on-chip valves for fluid control to individually addressable cell culture chambers with thin glass bottoms for high-resolution imaging. We developed a robust protocol for on-chip culturing of mouse ESCs for minimum of 3 days, to carry out experiments reliably and repeatedly. The on-chip ESC growth rate was similar to that on standard culture plates with same initial cell density. We tested the chips for high-resolution, time-lapse imaging of a sensitive reporter of ESC lineage priming, Nanog-GFP, and HHex-Venus with an H2B-mCherry nuclear marker for cell-tracking. Two color imaging of cells was possible over a 24-hr period while maintaining cell viability. Importantly, changing the media did not affect our ability to track individual cells. This system now enables long-term fluorescence imaging studies in a reliable and automated manner in a fully controlled microenvironment.

Identifiers

PMID31558920
PMCPMC6748857

What OpenQuestion holds

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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.