Evidence map›Paper›PMID 26768888›Full record

ArticleJournal of nanobiotechnology2016

Semi-automated quantification of living cells with internalized nanostructures.

Michael Bogdan Margineanu, Khachatur Julfakyan, Christoph Sommer, Jose Efrain Perez, Maria Fernanda Contreras, Niveen Khashab, Jürgen Kosel, Timothy Ravasi

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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.

Michael Bogdan MargineanuDivision of Biological and Environmental Sciences and Engineering, KAUST Environmental Epigenetic Program (KEEP), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Kingdom of Saudi Arabia. michael.margineanu@kaust.edu.sa.
Khachatur JulfakyanDivision of Physical Science and Engineering, Smart Hybrid Materials Laboratory (SHMs), King Abdullah University of Science and Technology,, Thuwal, Kingdom of Saudi Arabia. khachatur.julfakyan@kaust.edu.sa.
Christoph SommerInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Dr. Bohr-Gasse 3, Vienna, 1030, Austria. christoph.sommer@imba.oeaw.ac.at.
Jose Efrain PerezDivision of Biological and Environmental Sciences and Engineering, KAUST Environmental Epigenetic Program (KEEP), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Kingdom of Saudi Arabia. Jose.perez@kaust.edu.sa.
Maria Fernanda ContrerasDivision of Biological and Environmental Sciences and Engineering, KAUST Environmental Epigenetic Program (KEEP), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Kingdom of Saudi Arabia. maria.contreras@kaust.edu.sa.
Niveen KhashabDivision of Physical Science and Engineering, Smart Hybrid Materials Laboratory (SHMs), King Abdullah University of Science and Technology,, Thuwal, Kingdom of Saudi Arabia. niveen.khashab@kaust.edu.sa.
Jürgen KoselDivision of Computer, Electrical and Mathematical Sciences and Engineering, King Abdullah University of Science and Technology, Thuwal, Kingdom of Saudi Arabia. jurgen.kosel@kaust.edu.sa.
Timothy RavasiDivision of Biological and Environmental Sciences and Engineering, KAUST Environmental Epigenetic Program (KEEP), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Kingdom of Saudi Arabia. timothy.ravasi@kaust.edu.sa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNanostructures fabricated by different methods have become increasingly important for various applications in biology and medicine, such as agents for medical imaging or cancer therapy. In order to understand their interaction with living cells and their internalization kinetics, several attempts have been made in tagging them. Although methods have been developed to measure the number of nanostructures internalized by the cells, there are only few approaches aimed to measure the number of cells that internalize the nanostructures, and they are usually limited to fixed-cell studies. Flow cytometry can be used for live-cell assays on large populations of cells, however it is a single time point measurement, and does not include any information about cell morphology. To date many of the observations made on internalization events are limited to few time points and cells.

resultsIn this study, we present a method for quantifying cells with internalized magnetic nanowires (NWs). A machine learning-based computational framework, CellCognition, is adapted and used to classify cells with internalized and no internalized NWs, labeled with the fluorogenic pH-dependent dye pHrodo™ Red, and subsequently to determine the percentage of cells with internalized NWs at different time points. In a "proof-of-concept", we performed a study on human colon carcinoma HCT 116 cells and human epithelial cervical cancer HeLa cells interacting with iron (Fe) and nickel (Ni) NWs.

conclusionsThis study reports a novel method for the quantification of cells that internalize a specific type of nanostructures. This approach is suitable for high-throughput and real-time data analysis and has the potential to be used to study the interaction of different types of nanostructures in live-cell assays.

Indexed as

Biological AssayCell Line, TumorColonic NeoplasmsFemaleHCT116 CellsHeLa CellsHumansIronMagneticsNanostructuresNanowiresNickelParticle SizeUterine Cervical NeoplasmsIronNickel

Identifiers

PMID26768888
PMCPMC4714438

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LicenceCC BY
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Registered trials

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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.