Evidence map›Paper›PMID 25553183›Full record

ArticleBiomicrofluidics2014

Increasing label-free stem cell sorting capacity to reach transplantation-scale throughput.

Melinda G Simon, Ying Li, Janahan Arulmoli, Lisa P McDonnell, Adnan Akil, Jamison L Nourse, Abraham P Lee, Lisa A Flanagan

Abstract read
In one paragraph

Article in Biomicrofluidics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  17. High-throughput, low-loss, low-cost, and label-free cell separation using electrophysiology-activated cell enrichment.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

8 authors.

Melinda G SimonDepartment of Biomedical Engineering, University of California at Irvine , Irvine, California 92697, USA.ORCID 0000-0002-1509-2847
Ying LiDepartment of Neurology and Sue and Bill Gross Stem Cell Research Center, University of California at Irvine , Irvine, California 92697, USA.
Janahan Arulmoli
Lisa P McDonnellDepartment of Neurology and Sue and Bill Gross Stem Cell Research Center, University of California at Irvine , Irvine, California 92697, USA.
Adnan AkilDepartment of Neurology and Sue and Bill Gross Stem Cell Research Center, University of California at Irvine , Irvine, California 92697, USA.ORCID 0000-0002-3120-4642
Jamison L NourseDepartment of Neurology and Sue and Bill Gross Stem Cell Research Center, University of California at Irvine , Irvine, California 92697, USA.
Abraham P Lee
Lisa A Flanagan

Funding

Training Program in Stem Cell Translational Medicine for Neurological DisordersT32NS082174 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PETER John DONOVAN, Leslie Michels Thompson · 2013 to 2026
$3.3M
NINDS NIH HHS T32 NS082174
6 · The paper itself

Abstract

Dielectrophoresis (DEP) has proven an invaluable tool for the enrichment of populations of stem and progenitor cells owing to its ability to sort cells in a label-free manner and its biological safety. However, DEP separation devices have suffered from a low throughput preventing researchers from undertaking studies requiring large numbers of cells, such as needed for cell transplantation. We developed a microfluidic device designed for the enrichment of stem and progenitor cell populations that sorts cells at a rate of 150,000 cells/h, corresponding to an improvement in the throughput achieved with our previous device designs by over an order of magnitude. This advancement, coupled with data showing the DEP-sorted cells retain their enrichment and differentiation capacity when expanded in culture for periods of up to 2 weeks, provides sufficient throughput and cell numbers to enable a wider variety of experiments with enriched stem and progenitor cell populations. Furthermore, the sorting devices presented here provide ease of setup and operation, a simple fabrication process, and a low associated cost to use that makes them more amenable for use in common biological research laboratories. To our knowledge, this work represents the first to enrich stem cells and expand them in culture to generate transplantation-scale numbers of differentiation-competent cells using DEP.

Identifiers

PMID25553183
PMCPMC4240779

What OpenQuestion holds

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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.