Evidence map›Paper›PMID 37163318›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Characterization of Chemotaxis-Associated Gene Dysregulation in Myeloid Cell Populations in the Lungs during Lipopolysaccharide-Mediated Acute Lung Injury.

Bryan Latrell Holloman, Alkeiver Cannon, Kiesha Wilson, Narendra Singh, Mitzi Nagarkatti, Prakash Nagarkatti

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. 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
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 8 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

6 authors at 1 institution in 1 country.

Bryan Latrell HollomanDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.ORCID 0000-0002-9891-9001
Alkeiver CannonDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.ORCID 0000-0001-9558-603X
Kiesha WilsonDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.ORCID 0000-0001-8550-3739
Narendra SinghDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.
Mitzi NagarkattiDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.ORCID 0000-0002-5977-5615
Prakash NagarkattiDepartment of Pathology, Microbiology, and Immunology, University of South Carolina School of Medicine, Columbia, SC.ORCID 0000-0003-2663-0759
University of South Carolina · US

Funding

Targeting early ceramide elevation in pre-symptomatic eczemaP20GM103641 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ENOS, REILLY, NAGARKATTI, PRAKASH S · 2012 to 2023
$20.7M
Use of Resveratrol to treat experimental multiple sclerosisP01AT003961 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, PRAKASH S · 2007 to 2018
$14.2M
Role of the environmental sensor, AhR on colitisR01AI160896 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2021 to 2025
$2.6M
Epigenetic mechanisms in Transgenerational Effects of an Environmental PollutantR01ES030144 · NIEHS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2019 to 2023
$2.5M
Epigenetic Mechanisms of T Cell Dysregulation in PTSDR01AI129788 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI · 2017 to 2021
$2.4M
TCDD-INDUCED APOPTOSIS EFFECT ON T CELLSR01ES009098 · NIEHS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI NAGARKATTI, PRAKASH S · 1999 to 2008
$2.2M
AhR ligands in epigenetic dysregulation of T cellsR01AI123947 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2017 to 2021
$1.8M
Immunopathological basis of PTSDR01MH094755 · NIMH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, PRAKASH S · 2011 to 2015
$1.7M
Estrogen-T cell InteractionsR01ES019313 · NIEHS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2010 to 2014
$1.5M
Cannabinoid-induced apoptosis in T cell regulationR01DA016545 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NAGARKATTI, PRAKASH S. · 2003 to 2007
$1.2M
Role of Macrophages in CBD mediated attenuation of SEB-induced ARDSR00GM147910 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI WILSON, KIESHA · 2023 to 2025
$747k
Role of macrophages in CBD mediated attenuation of SEB-induced ARDSK99GM147910 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI WILSON, KIESHA · 2022 to 2023
$163k
NCCIH NIH HHS P01 AT003961NIAID NIH HHS R01 AI123947NIAID NIH HHS R01 AI129788NIAID NIH HHS R01 AI160896NIDA NIH HHS R01 DA016545NIEHS NIH HHS R01 ES009098NIEHS NIH HHS R01 ES019313NIEHS NIH HHS R01 ES030144NIGMS NIH HHS K99 GM147910NIGMS NIH HHS P20 GM103641NIGMS NIH HHS R00 GM147910NIMH NIH HHS R01 MH094755
6 · The paper itself

Abstract

During endotoxin-induced acute lung injury (ALI), immune cell recruitment resulting from chemotaxis is mediated by CXC and CC chemokines and their receptors. In this study, we investigated the role of chemokines and their receptors in the regulation of myeloid cell populations in the circulation and the lungs of C57BL/6J mice exhibiting LPS-mediated ALI using single-cell RNA sequencing. During ALI, there was an increase in the myeloid cells, M1 macrophages, monocytes, neutrophils, and other granulocytes, whereas there was a decrease in the residential alveolar macrophages and M2 macrophages. Interestingly, LPS triggered the upregulation of CCL3, CCL4, CXCL2/3, and CXCL10 genes associated with cellular migration of various subsets of macrophages, neutrophils, and granulocytes. Furthermore, there was an increase in the frequency of myeloid cells expressing CCR1, CCR3, CCR5, and CXCR2 receptors during ALI. MicroRNA sequencing studies of vehicle versus LPS groups identified several dysregulated microRNAs targeting the upregulated chemokine genes. This study suggests that chemokine ligand-receptors interactions are responsible for myeloid cell heterogenicity and cellular recruitment to the lungs during ALI. The single-cell transcriptomics allowed for an in-depth assessment and characterization of myeloid cells involved in immune cell trafficking during ALI.

Indexed as

Acute Lung InjuryChemotaxisAnimalsChemokinesLipopolysaccharidesLungMiceMice, Inbred C57BLMyeloid CellsReceptors, ChemokineChemokinesLipopolysaccharidesReceptors, Chemokine

Identifiers

PMID37163318
PMCPMC10615667
OpenAlexW4376121683

What OpenQuestion holds

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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.