Evidence map›Paper›PMID 38858477›Full record

ArticleScientific reports2024

Detection of CLCF1 protein expression by flow cytometry.

Véronique Laplante, Marine Rousseau, Félix Lombard-Vadnais, Ulysse Nadeau, Agathe Nazha, Jean-François Schmouth, Mukut Sharma, Sylvie Lesage, Jean-François Gauchat, Sarah Pasquin

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Véronique LaplanteDépartement de pharmacologie et physiologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Marine RousseauDépartement de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Félix Lombard-VadnaisCentre de recherche de l'Hôpital Maisonneuve-Rosemont, Université de Montréal, Montréal, QC, H1T 4B3, Canada.
Ulysse NadeauDépartement de pharmacologie et physiologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Agathe NazhaDépartement de pharmacologie et physiologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Jean-François SchmouthCentre de recherche du CHUM, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Mukut SharmaRenal Division, Kansas City Veterans Affairs Medical Center, Kansas City, MO, 64128-2226, USA.
Sylvie LesageDépartement de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Jean-François GauchatDépartement de pharmacologie et physiologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada.
Sarah PasquinDépartement de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, H3T 1J4, Canada. sarah.pasquin@umontreal.ca.

Funding

CIHR PTJ 159654
6 · The paper itself

Abstract

Cardiotrophin-like cytokine factor 1 (CLCF1) is an IL-6 family cytokine with neurotrophic and immuno-modulating functions. CLCF1 mRNA has been detected in primary and secondary lymphoid organs, and up-regulation of CLCF1 mRNA levels has been associated with the T helper (Th) 17 polarization. However, information regarding CLCF1 expression by immune cells at the protein level remains scarce. We have developed a methodology that uses a monoclonal antibody (mAb) directed against CLCF1 for the detection of human and mouse CLCF1 by flow cytometry. We have successfully detected CLCF1 protein expression in cells from the mouse pro-B cell line Ba/F3 that were transduced with CLCF1 cDNA. Interestingly, we found that the anti-CLCF1 mAb inhibits CLCF1 biological activity in vitro by binding to an epitope that encompasses site III of the cytokine. Moreover, we have detected CLCF1 expression in mouse splenic T cells, as well as in vitro differentiated Th1 cells. The specificity of the fluorescence signal was demonstrated using Clcf1-deficient lymphocytes generated using a conditional knock-out mouse model. The detection of CLCF1 protein by flow cytometry will be a valuable tool to study CLCF1 expression during normal and pathological immune responses.

Indexed as

Antibodies, MonoclonalCytokinesFlow CytometryAnimalsCell LineHumansMiceMice, KnockoutTh1 CellsAntibodies, MonoclonalCytokines

Identifiers

PMID38858477
PMCPMC11164924

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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.