Cell shape sensing licenses dendritic cells for homeostatic migration to lymph nodes

细胞形状感知使树突状细胞能够进行向淋巴结的稳态迁移。

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作者:Zahraa Alraies ,Claudia A Rivera ,Maria-Graciela Delgado # ,Doriane Sanséau # ,Mathieu Maurin ,Roberto Amadio ,Giulia Maria Piperno ,Garett Dunsmore ,Aline Yatim ,Livia Lacerda Mariano ,Anna Kniazeva ,Vincent Calmettes ,Pablo J Sáez ,Alice Williart ,Henri Popard ,Matthieu Gratia ,Olivier Lamiable ,Aurélie Moreau ,Zoé Fusilier ,Lou Crestey ,Benoit Albaud ,Patricia Legoix ,Anne S Dejean ,Anne-Louise Le Dorze ,Hideki Nakano ,Donald N Cook ,Toby Lawrence ,Nicolas Manel ,Federica Benvenuti ,Florent Ginhoux ,Hélène D Moreau ,Guilherme P F Nader ,Matthieu Piel ,Ana-Maria Lennon-Duménil

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 IKKβ-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.

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