Evidence map›Paper›PMID 37575382›Full record

ArticleBio-protocol2023

Label-free Chemical Characterization of Polarized Immune Cells in vitro and Host Response to Implanted Bio-instructive Polymers in vivo Using 3D OrbiSIMS.

Waraporn Suvannapruk, Max K Edney, Leanne E Fisher, Jeni C Luckett, Dong-Hyun Kim, David J Scurr, Amir M Ghaemmaghami, Morgan R Alexander

Open access · diamondAbstract read
In one paragraph

Article in Bio-protocol, 2023. 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
0.1field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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 at 1 institution in 1 country.

Waraporn SuvannaprukAdvanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Max K EdneyDepartment of Chemical and Environmental Engineering, Faculty of Engineering, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Leanne E FisherImmunology & Immuno-bioengineering Group, School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Jeni C LuckettSchool of Life Sciences, Faculty of Medicine and Health Science, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Dong-Hyun KimAdvanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
David J ScurrAdvanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Amir M GhaemmaghamiImmunology & Immuno-bioengineering Group, School of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
Morgan R AlexanderAdvanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park Nottingham, NG7 2RD, UK.
University of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Three-dimensional OrbiTrap Secondary Ion Mass Spectrometry (3D OrbiSIMS) is a secondary ion mass spectrometry instrument, a combination of a Time of Flight (ToF) instrument with an Orbitrap analyzer. The 3D OrbiSIMS technique is a powerful tool for metabolic profiling in biological samples. This can be achieved at subcellular spatial resolution, high sensitivity, and high mass-resolving power coupled with MS/MS analysis. Characterizing the metabolic signature of macrophage subsets within tissue sections offers great potential to understand the response of the human immune system to implanted biomaterials. Here, we describe a protocol for direct analysis of individual cells after in vitro differentiation of naïve monocytes into M1 and M2 phenotypes using cytokines. As a first step in vivo, we investigate explanted silicon catheter sections as a medical device in a rodent model of foreign body response. Protocols are presented to allow the host response to different immune instructive materials to be compared. The first demonstration of this capability illustrates the great potential of direct cell and tissue section analysis for in situ metabolite profiling to probe functional phenotypes using molecular signatures. Details of the in vitro cell approach, materials, sample preparation, and explant handling are presented, in addition to the data acquisition approaches and the data analysis pipelines required to achieve useful interpretation of these complex spectra. This method is useful for in situ characterization of both in vitro single cells and ex vivo tissue sections. This will aid the understanding of the immune response to medical implants by informing the design of immune-instructive biomaterials with positive interactions. It can also be used to investigate a broad range of other clinically relevant therapeutics and immune dysregulations. Graphical overview.

Indexed as

3D OrbiSIMSMacrophageMetabolic profilingMonocytePBMC isolationSingle cell

Identifiers

PMID37575382
PMCPMC10415193
OpenAlexW4385608837

What OpenQuestion holds

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LicenceCC BY-NC
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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.