Evidence map›Paper›PMID 24193545›Full record

ArticleJournal of visualized experiments : JoVE2013

Autonomously bioluminescent mammalian cells for continuous and real-time monitoring of cytotoxicity.

Tingting Xu, Dan M Close, James D Webb, Steven A Ripp, Gary S Sayler

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Tingting XuThe Joint Institute for Biological Sciences, Oak Ridge National Laboratory.
Dan M Close
James D Webb
Steven A Ripp
Gary S Sayler

Funding

Expressing bacterial bioluminescence in human cell lines: Engineering autobioluminescent reporter cells to screen for endocrine disruptor chemicalsR44ES022567 · NIEHS · 490 BIOTECH, INC. · PI MORRISON, DAN · 2015 to 2016
$996k
Development of Noninvasive Bioluminescence Imaging for Cancer Diagnosis and TheraR21CA127745 · NCI · UNIVERSITY OF TENNESSEE KNOXVILLE · PI SAYLER, GARY S · 2007 to 2008
$239k
Expressing bacterial bioluminescence in human cell lines: Engineering autobiolumiR43ES022567 · NIEHS · 490 BIOTECH, INC. · PI MORRISON, DAN · 2013 to 2013
$138k
NCI NIH HHS CA127745-01NCI NIH HHS R21 CA127745NIEHS NIH HHS 1R43ES022567-01NIEHS NIH HHS R43 ES022567NIEHS NIH HHS R44 ES022567
6 · The paper itself

Abstract

Mammalian cell-based in vitro assays have been widely employed as alternatives to animal testing for toxicological studies but have been limited due to the high monetary and time costs of parallel sample preparation that are necessitated due to the destructive nature of firefly luciferase-based screening methods. This video describes the utilization of autonomously bioluminescent mammalian cells, which do not require the destructive addition of a luciferin substrate, as an inexpensive and facile method for monitoring the cytotoxic effects of a compound of interest. Mammalian cells stably expressing the full bacterial bioluminescence (luxCDABEfrp) gene cassette autonomously produce an optical signal that peaks at 490 nm without the addition of an expensive and possibly interfering luciferin substrate, excitation by an external energy source, or destruction of the sample that is traditionally performed during optical imaging procedures. This independence from external stimulation places the burden for maintaining the bioluminescent reaction solely on the cell, meaning that the resultant signal is only detected during active metabolism. This characteristic makes the lux-expressing cell line an excellent candidate for use as a biosentinel against cytotoxic effects because changes in bioluminescent production are indicative of adverse effects on cellular growth and metabolism. Similarly, the autonomous nature and lack of required sample destruction permits repeated imaging of the same sample in real-time throughout the period of toxicant exposure and can be performed across multiple samples using existing imaging equipment in an automated fashion.

Indexed as

Anti-Bacterial AgentsBleomycinHEK293 CellsHumansLuciferasesLuminescent MeasurementsToxicity TestsAnti-Bacterial AgentsBleomycinLuciferases

Identifiers

PMID24193545
PMCPMC3995105

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.