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The Transcription Factor ZEB2 Is Required to Maintain the Tissue-Specific Identities of Macrophages.
Scott, Charlotte L; T'Jonck, Wouter; Martens, Liesbet; Todorov, Helena; Sichien, Dorine; Soen, Bieke; Bonnardel, Johnny; De Prijck, Sofie; Vandamme, Niels; Cannoodt, Robrecht; Saelens, Wouter; Vanneste, Bavo; Toussaint, Wendy; De Bleser, Pieter; Takahashi, Nozomi; Vandenabeele, Peter; Henri, Sandrine; Pridans, Clare; Hume, David A; Lambrecht, Bart N; De Baetselier, Patrick; Milling, Simon W F; Van Ginderachter, Jo A; Malissen, Bernard; Berx, Geert; Beschin, Alain; Saeys, Yvan; Guilliams, Martin.
Afiliação
  • Scott CL; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Scie
  • T'Jonck W; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • Martens L; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Todorov H; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Sichien D; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • Soen B; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Molecular and Cellular Oncology Lab, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Bonnardel J; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • De Prijck S; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • Vandamme N; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Molecular and Cellular Oncology Lab, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Cannoodt R; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Saelens W; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Vanneste B; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • Toussaint W; Laboratory of Mucosal Immunology and Immunoregulation, VIB Center for Inflammation Research, Ghent, Belgium; Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
  • De Bleser P; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Takahashi N; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Laboratory of Molecular Signaling and Cell Death, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Vandenabeele P; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Laboratory of Molecular Signaling and Cell Death, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Henri S; Centre d'Immunologie de Marseille-Luminy, Aix Marseille Université, INSERM, CNRS 13288 Marseille, France.
  • Pridans C; MRC Centre for Inflammation Research, University of Edinburgh, The Queen's Medical Research Institute, UK.
  • Hume DA; Mater Research-University of Queensland, Translational Research Institute, Qld 4102, Australia.
  • Lambrecht BN; Laboratory of Mucosal Immunology and Immunoregulation, VIB Center for Inflammation Research, Ghent, Belgium; Department of Respiratory Medicine, Ghent University, Ghent, Belgium.
  • De Baetselier P; Myeloid Cell Immunology Lab, VIB-UGent Center for Inflammation Research, Brussels, Belgium; Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
  • Milling SWF; Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK.
  • Van Ginderachter JA; Myeloid Cell Immunology Lab, VIB-UGent Center for Inflammation Research, Brussels, Belgium; Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
  • Malissen B; Centre d'Immunologie de Marseille-Luminy, Aix Marseille Université, INSERM, CNRS 13288 Marseille, France; Centre d'Immunophénomique, Aix Marseille Université, INSERM, CNRS, 13288 Marseille, France.
  • Berx G; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium; Molecular and Cellular Oncology Lab, VIB-UGent Center for Inflammation Research, Ghent, Belgium.
  • Beschin A; Myeloid Cell Immunology Lab, VIB-UGent Center for Inflammation Research, Brussels, Belgium; Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
  • Saeys Y; Data Mining and Modeling for Biomedicine, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium.
  • Guilliams M; Laboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB-UGent Center for Inflammation Research, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium. Electronic address: martin.guilliams@irc.vib-ugent.be.
Immunity ; 49(2): 312-325.e5, 2018 08 21.
Article em En | MEDLINE | ID: mdl-30076102
ABSTRACT
Heterogeneity between different macrophage populations has become a defining feature of this lineage. However, the conserved factors defining macrophages remain largely unknown. The transcription factor ZEB2 is best described for its role in epithelial to mesenchymal transition; however, its role within the immune system is only now being elucidated. We show here that Zeb2 expression is a conserved feature of macrophages. Using Clec4f-cre, Itgax-cre, and Fcgr1-cre mice to target five different macrophage populations, we found that loss of ZEB2 resulted in macrophage disappearance from the tissues, coupled with their subsequent replenishment from bone-marrow precursors in open niches. Mechanistically, we found that ZEB2 functioned to maintain the tissue-specific identities of macrophages. In Kupffer cells, ZEB2 achieved this by regulating expression of the transcription factor LXRα, removal of which recapitulated the loss of Kupffer cell identity and disappearance. Thus, ZEB2 expression is required in macrophages to preserve their tissue-specific identities.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores X do Fígado / Homeobox 2 de Ligação a E-box com Dedos de Zinco / Células de Kupffer Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores X do Fígado / Homeobox 2 de Ligação a E-box com Dedos de Zinco / Células de Kupffer Idioma: En Ano de publicação: 2018 Tipo de documento: Article