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Differential expression and regulation of MS4A family members in myeloid cells in physiological and pathological conditions

Authors :
Fabio Grizzi
Alberto Mantovani
Domenico Supino
Fabio Pasqualini
Marie-Astrid Boutet
Andrea Gianatti
Marina Sironi
Maria José Oliveira
Barbara Bottazzi
Silvia Carnevale
Matteo Stravalaci
Sarah N. Mapelli
Irene Mattiola
C. Pitzalis
Rémi Porte
Rita Silva-Gomes
Federico Colombo
Massimo Locati
Humanitas University [Milan] (Hunimed)
Universidade do Porto
Istituto Clinico Humanitas [Milan] (IRCCS Milan)
Regenerative Medicine and Skeleton research lab (RMeS)
Ecole Nationale Vétérinaire, Agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS)-Centre hospitalier universitaire de Nantes (CHU Nantes)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE)
Université de Nantes (UN)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Queen Mary University of London (QMUL)
Berlin Institute of Health (BIH)
Charité - UniversitätsMedizin = Charité - University Hospital [Berlin]
Mucosal and Developmental Immunology [Berlin, Germany]
IRCCS San Raffaele Scientific Institute [Milan, Italie]
Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Azienda Ospedaliera Ospedale Papa Giovanni XXIII [Bergamo, Italy]
University of Milan
Federal University of Health Sciences of Porto Alegre = Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA)
Universidade do Porto = University of Porto
Regenerative Medicine and Skeleton (RMeS)
École nationale vétérinaire, agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre hospitalier universitaire de Nantes (CHU Nantes)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE)
Université de Nantes (UN)-Université de Nantes (UN)
Università degli Studi di Milano = University of Milan (UNIMI)
Jehan, Frederic
Source :
Journal of Leukocyte Biology, Journal of Leukocyte Biology, Society for Leukocyte Biology, 2021, Online ahead of print. ⟨10.1002/JLB.2A0421-200R⟩, Journal of Leukocyte Biology, 2021, Online ahead of print. ⟨10.1002/JLB.2A0421-200R⟩
Publication Year :
2021

Abstract

The MS4A gene family encodes 18 tetraspanin-like proteins, most of which with unknown function. MS4A1 (CD20), MS4A2 (FcεRIβ), MS4A3 (HTm4), and MS4A4A play important roles in immunity, whereas expression and function of other members of the family are unknown. The present investigation was designed to obtain an expression fingerprint of MS4A family members, using bioinformatics analysis of public databases, RT-PCR, and protein analysis when possible. MS4A3, MS4A4A, MS4A4E, MS4A6A, MS4A7, and MS4A14 were expressed by myeloid cells. MS4A6A and MS4A14 were expressed in circulating monocytes and decreased during monocyte-to-Mϕ differentiation in parallel with an increase in MS4A4A expression. Analysis of gene expression regulation revealed a strong induction of MS4A4A, MS4A6A, MS4A7, and MS4A4E by glucocorticoid hormones. Consistently with in vitro findings, MS4A4A and MS4A7 were expressed in tissue Mϕs from COVID-19 and rheumatoid arthritis patients. Interestingly, MS4A3, selectively expressed in myeloid precursors, was found to be a marker of immature circulating neutrophils, a cellular population associated to COVID-19 severe disease. The results reported here show that members of the MS4A family are differentially expressed and regulated during myelomonocytic differentiation, and call for assessment of their functional role and value as therapeutic targets.

Details

ISSN :
19383673 and 07415400
Volume :
111
Issue :
4
Database :
OpenAIRE
Journal :
Journal of leukocyte biology
Accession number :
edsair.doi.dedup.....af7859fa1e2baddcf08909d9f18310c8
Full Text :
https://doi.org/10.1002/JLB.2A0421-200R⟩