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Cell shape sensing licenses dendritic cells for homeostatic migration to lymph nodes.
Alraies, Zahraa; Rivera, Claudia A; Delgado, Maria-Graciela; Sanséau, Doriane; Maurin, Mathieu; Amadio, Roberto; Maria Piperno, Giulia; Dunsmore, Garett; Yatim, Aline; Lacerda Mariano, Livia; Kniazeva, Anna; Calmettes, Vincent; Sáez, Pablo J; Williart, Alice; Popard, Henri; Gratia, Matthieu; Lamiable, Olivier; Moreau, Aurélie; Fusilier, Zoé; Crestey, Lou; Albaud, Benoit; Legoix, Patricia; Dejean, Anne S; Le Dorze, Anne-Louise; Nakano, Hideki; Cook, Donald N; Lawrence, Toby; Manel, Nicolas; Benvenuti, Federica; Ginhoux, Florent; Moreau, Hélène D; P F Nader, Guilherme; Piel, Matthieu; Lennon-Duménil, Ana-Maria.
Afiliação
  • Alraies Z; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Rivera CA; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Delgado MG; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Sanséau D; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Maurin M; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Amadio R; Cellular Immunology, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
  • Maria Piperno G; Cellular Immunology, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
  • Dunsmore G; INSERM U1015, Gustave Roussy Cancer Campus, Villejuif, France.
  • Yatim A; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Lacerda Mariano L; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Kniazeva A; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Calmettes V; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Sáez PJ; Cell Communication and Migration Laboratory, Institute of Biochemistry and Molecular Cell Biology, Center for Experimental Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Williart A; CNRS UMR144, Institut Curie, PSL Research University, Paris, France.
  • Popard H; CNRS UMR144, Institut Curie, PSL Research University, Paris, France.
  • Gratia M; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Lamiable O; Malaghan Institute of Medical Research, Wellington, New Zealand.
  • Moreau A; Center for Research in Transplantation and Translational Immunology, UMR 1064, INSERM, Nantes Université, Nantes, France.
  • Fusilier Z; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Crestey L; INSERM U932, Immunity and Cancer, Institut Curie, Paris-Cité University, Paris, France.
  • Albaud B; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Legoix P; Platform NGS-ICGEX, Institut Curie, Paris, France.
  • Dejean AS; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • Le Dorze AL; INSERM UMR1291, CNRS UMR5051, Institut Toulousain des Maladies Infectieuses et Inflammatoires (INFINITy), Université Toulouse III, Toulouse, France.
  • Nakano H; INSERM UMR1291, CNRS UMR5051, Institut Toulousain des Maladies Infectieuses et Inflammatoires (INFINITy), Université Toulouse III, Toulouse, France.
  • Cook DN; Immunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), Research Triangle Park, NC, USA.
  • Lawrence T; Immunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), Research Triangle Park, NC, USA.
  • Manel N; Centre d'Immunologie de Marseille-Luminy, INSERM, CNRS, Université Aix-Marseille, Marseille, France.
  • Benvenuti F; Centre for Inflammation Biology and Cancer Immunology, School of Immunology and Microbial Sciences, King's College London, London, UK.
  • Ginhoux F; Henan Key Laboratory of Immunology and Targeted Therapy, School of Laboratory Medicine, Xinxiang Medical University, Xinxiang, China.
  • Moreau HD; INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.
  • P F Nader G; Cellular Immunology, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
  • Piel M; INSERM U1015, Gustave Roussy Cancer Campus, Villejuif, France.
  • Lennon-Duménil AM; Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, Immunos, Singapore, Singapore.
Nat Immunol ; 25(7): 1193-1206, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38834865
ABSTRACT
Immune cells experience large cell shape changes during environmental patrolling because of the physical constraints that they encounter while migrating through tissues. These cells can adapt to such deformation events using dedicated shape-sensing pathways. However, how shape sensing affects immune cell function is mostly unknown. Here, we identify a shape-sensing mechanism that increases the expression of the chemokine receptor CCR7 and guides dendritic cell migration from peripheral tissues to lymph nodes at steady state. This mechanism relies on the lipid metabolism enzyme cPLA2, requires nuclear envelope tensioning and is finely tuned by the ARP2/3 actin nucleation complex. We also show that this shape-sensing axis reprograms dendritic cell transcription by activating an IKKß-NF-κB-dependent pathway known to control their tolerogenic potential. These results indicate that cell shape changes experienced by immune cells can define their migratory behavior and immunoregulatory properties and reveal a contribution of the physical properties of tissues to adaptive immunity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Movimento Celular / Receptores CCR7 / Homeostase / Linfonodos / Camundongos Endogâmicos C57BL Limite: Animals Idioma: En Revista: Nat Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Dendríticas / Movimento Celular / Receptores CCR7 / Homeostase / Linfonodos / Camundongos Endogâmicos C57BL Limite: Animals Idioma: En Revista: Nat Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França
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