Evidence map›Paper›PMID 28671651›Full record

ArticleJournal of visualized experiments : JoVE2017

An All-on-chip Method for Rapid Neutrophil Chemotaxis Analysis Directly from a Drop of Blood.

Ke Yang, Jiandong Wu, Ling Zhu, Yong Liu, Michael Zhang, Francis Lin

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. 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
0.4field-weighted citation impact, top 39% 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, 11 citations in OpenAlex.

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  6. Microfluidic devices for neutrophil chemotaxis studies.Journal of translational medicine · 2020
    Review
  7. Review
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 4 institutions in 2 countries.

Ke YangInstitute of Applied Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences; University of Science and Technology of China; Department of Physics and Astronomy, University of Manitoba.
Jiandong WuDepartment of Physics and Astronomy, University of Manitoba; Department of Biosystems Engineering, University of Manitoba.
Ling ZhuInstitute of Applied Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences.
Yong LiuInstitute of Applied Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences.
Michael ZhangSeven Oaks General Hospital.
Francis LinDepartment of Physics and Astronomy, University of Manitoba; Department of Biosystems Engineering, University of Manitoba; Department of Immunology, University of Manitoba; Department of Biological Sciences, University of Manitoba; Francis.Lin@umanitoba.ca.
Chinese Academy of Sciences · CNUniversity of Manitoba · CASeven Oaks General Hospital · CAUniversity of Science and Technology of China · CN

Funding

CIHR 134755-1
6 · The paper itself

Abstract

Neutrophil migration and chemotaxis are critical for our body's immune system. Microfluidic devices are increasingly used for investigating neutrophil migration and chemotaxis owing to their advantages in real-time visualization, precise control of chemical concentration gradient generation, and reduced reagent and sample consumption. Recently, a growing effort has been made by the microfluidic researchers toward developing integrated and easily operated microfluidic chemotaxis analysis systems, directly from whole blood. In this direction, the first all-on-chip method was developed for integrating the magnetic negative purification of neutrophils and the chemotaxis assay from small blood volume samples. This new method permits a rapid sample-to-result neutrophil chemotaxis test in 25 min. In this paper, we provide detailed construction, operation and data analysis method for this all-on-chip chemotaxis assay with a discussion on troubleshooting strategies, limitations and future directions. Representative results of the neutrophil chemotaxis assay testing a defined chemoattractant, N-Formyl-Met-Leu-Phe (fMLP), and sputum from a chronic obstructive pulmonary disease (COPD) patient, using this all-on-chip method are shown. This method is applicable to many cell migration-related investigations and clinical applications.

Indexed as

Lab-On-A-Chip DevicesCell Migration Assays, LeukocyteChemotactic FactorsChemotaxis, LeukocyteHumansMicrofluidicsNeutrophilsN-Formylmethionine Leucyl-PhenylalaninePulmonary Disease, Chronic ObstructiveSputumChemotactic Factorsmethionyl-leucyl-phenylalanineN-Formylmethionine Leucyl-Phenylalanine

Identifiers

PMID28671651
PMCPMC5511520
OpenAlexW2682055778

What OpenQuestion holds

Textmetadata
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.