Evidence map›Paper›PMID 31852428›Full record

ArticleBMC bioinformatics2019

Deriving a Boolean dynamics to reveal macrophage activation with in vitro temporal cytokine expression profiles.

Ricardo Ramirez, Allen Michael Herrera, Joshua Ramirez, Chunjiang Qian, David W Melton, Paula K Shireman, Yu-Fang Jin

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Ricardo RamirezDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX, 78249, USA.
Allen Michael HerreraDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX, 78249, USA.
Joshua RamirezDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX, 78249, USA.
Chunjiang QianDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX, 78249, USA.
David W MeltonDepartment of Anesthesia, Critical Care and Pain Medicine, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, 02215, USA.
Paula K ShiremanDepartment of Surgery, Long School of Medicine, University of Texas Health Science Center San Antonio, 7703 Floyd Curl Dr, San Antonio, TX, 78229, USA.
Yu-Fang JinDepartment of Electrical and Computer Engineering, The University of Texas at San Antonio, 1 UTSA Circle, San Antonio, TX, 78249, USA. Yufang.Jin@utsa.edu.ORCID http://orcid.org/0000-0002-7421-527X
The University of Texas at San Antonio · USBeth Israel Deaconess Medical Center · USThe University of Texas Health Science Center at San Antonio · US

Funding

CHEMOKINES AND IMMUNE CELLS IN HIND LIMB ISCHEMIAR01HL074236 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHIREMAN, PAULA K · 2003 to 2011
$3.0M
Improved Muscle Regeneration by Anti-miRNA Alteration in Macrophage PolarizationF30HL110743 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MELTON, DAVID · 2011 to 2015
$158k
MicroRNA Regulation of Macrophage Polarization in Muscle RegenerationI01BX001186 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI SHIREMAN, PAULA K · 2012 to 2015
–
BLRD VA I01 BX000186NHLBI NIH HHS F30 HL110743NHLBI NIH HHS R01 HL074236NIH HHS F30HL110743NIH HHS R01HL074236
6 · The paper itself

Abstract

backgroundMacrophages show versatile functions in innate immunity, infectious diseases, and progression of cancers and cardiovascular diseases. These versatile functions of macrophages are conducted by different macrophage phenotypes classified as classically activated macrophages and alternatively activated macrophages due to different stimuli in the complex in vivo cytokine environment. Dissecting the regulation of macrophage activations will have a significant impact on disease progression and therapeutic strategy. Mathematical modeling of macrophage activation can improve the understanding of this biological process through quantitative analysis and provide guidance to facilitate future experimental design. However, few results have been reported for a complete model of macrophage activation patterns.

resultsWe globally searched and reviewed literature for macrophage activation from PubMed databases and screened the published experimental results. Temporal in vitro macrophage cytokine expression profiles from published results were selected to establish Boolean network models for macrophage activation patterns in response to three different stimuli. A combination of modeling methods including clustering, binarization, linear programming (LP), Boolean function determination, and semi-tensor product was applied to establish Boolean networks to quantify three macrophage activation patterns. The structure of the networks was confirmed based on protein-protein-interaction databases, pathway databases, and published experimental results. Computational predictions of the network evolution were compared against real experimental results to validate the effectiveness of the Boolean network models.

conclusionThree macrophage activation core evolution maps were established based on the Boolean networks using Matlab. Cytokine signatures of macrophage activation patterns were identified, providing a possible determination of macrophage activations using extracellular cytokine measurements.

Indexed as

Macrophage ActivationCytokinesMacrophagesModels, TheoreticalCytokinesBoolean networksCytokinesInflammationMacrophage polarization

Identifiers

PMID31852428
PMCPMC6921543
OpenAlexW2996208149

What OpenQuestion holds

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LicenceCC BY
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.