PIR-B Regulates CD4

Animals Biomarkers Cell Survival / genetics Colitis / etiology Disease Models, Animal Disease Susceptibility Gene Expression Profiling Gene Expression Regulation Immunohistochemistry Immunologic Memory Immunomodulation Immunophenotyping Inflammatory Bowel Diseases / etiology Interleukin-10 / genetics Interleukin-17 / metabolism Intestinal Mucosa / immunology Mice Mice, Knockout Receptors, Immunologic / genetics Signal Transduction T-Lymphocyte Subsets / immunology
CD4(+) T Cells Inflammatory Bowel Disease Interleukin 17 Paired Immunoglobulin Receptor

Journal

Cellular and molecular gastroenterology and hepatology
ISSN: 2352-345X
Titre abrégé: Cell Mol Gastroenterol Hepatol
Pays: United States
ID NLM: 101648302

Informations de publication

Date de publication:
2021
Historique:
received: 02 06 2021
revised: 16 06 2021
accepted: 17 06 2021
pubmed: 10 7 2021
medline: 26 3 2022
entrez: 9 7 2021
Statut: ppublish

Résumé

CD4 We used Il10 We identified PIR-B expression on memory CD4 Our findings show an intrinsic role for PIR-B/LILRB3 in the regulation of CD4

Sections du résumé

BACKGROUND & AIMS
CD4
METHODS
We used Il10
RESULTS
We identified PIR-B expression on memory CD4
CONCLUSIONS
Our findings show an intrinsic role for PIR-B/LILRB3 in the regulation of CD4

Identifiants

DOI: 10.1016/j.jcmgh.2021.06.013 PMID: 34242819 PMC: PMC8531983
pubmed: 34242819
pii: S2352-345X(21)00128-4
doi: 10.1016/j.jcmgh.2021.06.013
pmc: PMC8531983
pii:
doi:

Substances chimiques

Biomarkers 0
Interleukin-17 0
Pirb protein, mouse 0
Receptors, Immunologic 0
Interleukin-10 130068-27-8

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1479-1502

Subventions

Organisme : NIDDK NIH HHS
ID : F31 DK125007
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI138177
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK034933
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK090119
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK099222
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007413
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI112626
Pays : United States

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jazib Uddin (J)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan; Graduate Program in Immunology, Ann Arbor, Michigan.

Sunil Tomar (S)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan.

Ankit Sharma (A)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan.

Lisa Waggoner (L)

Division of Allergy and Immunology, Cincinnati, Ohio.

Varsha Ganesan (V)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan.

Sahiti Marella (S)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan.

Yanfen Yang (Y)

Division of Allergy and Immunology, Cincinnati, Ohio.

Taeko Noah (T)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan.

Simone Vanoni (S)

Division of Allergy and Immunology, Cincinnati, Ohio.

Andrew Patterson (A)

Division of Immunobiology, Cincinnati, Ohio.

Chang Zeng (C)

Division of Allergy and Immunology, Cincinnati, Ohio.

Paul S Foster (PS)

School of Biomedical Sciences and Pharmacy, University of Newcastle and Hunter Medical Research Institute, Newcastle, Australia.

Rodney Newberry (R)

Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.

Shrinivas Bishu (S)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Ann Arbor, Michigan.

John Y Kao (JY)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Ann Arbor, Michigan.

Michael J Rosen (MJ)

Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Cincinnati, Ohio.

Lee Denson (L)

Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Cincinnati, Ohio.

Philip D King (PD)

Department of Microbiology and Immunology, Ann Arbor, Michigan.

Kasper Hoebe (K)

Division of Immunobiology, Cincinnati, Ohio; Janssen, Inc, Janssen R@D, Discovery, Innate Immunology Spring House, Pennsylvania.

Senad Divanovic (S)

Division of Immunobiology, Cincinnati, Ohio; Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.

Ariel Munitz (A)

Department of Clinical Microbiology and Immunology, Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel.

Simon P Hogan (SP)

Division of Experimental Pathology, Department of Pathology, Ann Arbor, Michigan; Mary H Weiser Food Allergy Center, Michigan Medicine, University of Michigan, Ann Arbor, Michigan. Electronic address: sihogan@med.umich.edu.

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Classifications MeSH

questionsmedicales.fr › Eucaryotes › Animaux › PIR-B Regulates CD4
questionsmedicales.fr › Facteurs biologiques › Marqueurs biologiques › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes physiologiques cellulaires › Survie cellulaire › PIR-B Regulates CD4
questionsmedicales.fr › Maladies de l'appareil digestif › Maladies gastro-intestinales › Maladies intestinales › Maladies du côlon › Colite › PIR-B Regulates CD4
questionsmedicales.fr › Techniques d'investigation › Modèles théoriques › Modèles biologiques › Modèles animaux de maladie humaine › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes physiologiques › Constitution physique › Prédisposition aux maladies › PIR-B Regulates CD4
questionsmedicales.fr › Techniques d'investigation › Techniques génétiques › Analyse de profil d'expression de gènes › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes génétiques › Régulation de l'expression des gènes › PIR-B Regulates CD4
questionsmedicales.fr › Disciplines des sciences naturelles › Chimie › Biochimie › Immunohistochimie › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes du système immunitaire › Immunité › Immunité acquise › Mémoire immunologique › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes du système immunitaire › Immunomodulation › PIR-B Regulates CD4
questionsmedicales.fr › Techniques d'investigation › Techniques immunologiques › Tests immunologiques › Immunophénotypage › PIR-B Regulates CD4
questionsmedicales.fr › Maladies de l'appareil digestif › Maladies gastro-intestinales › Maladies intestinales › Maladies inflammatoires intestinales › PIR-B Regulates CD4
questionsmedicales.fr › Facteurs biologiques › Protéines et peptides de signalisation intercellulaire › Cytokines › Interleukines › Interleukine-10 › PIR-B Regulates CD4
questionsmedicales.fr › Facteurs biologiques › Protéines et peptides de signalisation intercellulaire › Cytokines › Interleukines › Interleukine-17 › PIR-B Regulates CD4
questionsmedicales.fr › Tissus › Membranes › Muqueuse › Muqueuse intestinale › PIR-B Regulates CD4
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Rodentia › Muridae › Murinae › Souris › PIR-B Regulates CD4
questionsmedicales.fr › Eucaryotes › Animaux › Chordés › Vertébrés › Mammifères › Eutheria › Rodentia › Muridae › Murinae › Souris › Souris transgéniques › Souris knockout › PIR-B Regulates CD4
questionsmedicales.fr › Acides aminés, peptides et protéines › Protéines › Protéines membranaires › Récepteurs de surface cellulaire › Récepteurs immunologiques › PIR-B Regulates CD4
questionsmedicales.fr › Phénomènes physiologiques cellulaires › Transduction du signal › PIR-B Regulates CD4
questionsmedicales.fr › Systèmes sanguin et immunitaire › Système immunitaire › Leucocytes › Agranulocytes › Lymphocytes › Lymphocytes T › Sous-populations de lymphocytes T › PIR-B Regulates CD4