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

被引:13
|
作者
Alraies, Zahraa [1 ]
Rivera, Claudia A. [1 ]
Delgado, Maria-Graciela [1 ]
Sanseau, Doriane [1 ]
Maurin, Mathieu [1 ]
Amadio, Roberto [2 ]
Maria Piperno, Giulia [2 ]
Dunsmore, Garett [3 ]
Yatim, Aline [1 ]
Lacerda Mariano, Livia [1 ]
Kniazeva, Anna [1 ]
Calmettes, Vincent [1 ]
Saez, Pablo J. [4 ]
Williart, Alice [5 ]
Popard, Henri [5 ]
Gratia, Matthieu [1 ]
Lamiable, Olivier [6 ]
Moreau, Aurelie [7 ]
Fusilier, Zoe [1 ,8 ]
Crestey, Lou [1 ]
Albaud, Benoit [9 ]
Legoix, Patricia [1 ]
Dejean, Anne S. [10 ]
Le Dorze, Anne-Louise [10 ]
Nakano, Hideki [11 ]
Cook, Donald N. [11 ]
Lawrence, Toby [12 ,13 ,14 ]
Manel, Nicolas [1 ]
Benvenuti, Federica [2 ]
Ginhoux, Florent [3 ,15 ,16 ,17 ]
Moreau, Helene D. [1 ]
P. F. Nader, Guilherme [5 ,18 ]
Piel, Matthieu [5 ]
Lennon-Dumenil, Ana-Maria [1 ]
机构
[1] PSL Univ, Inst Curie, INSERM U932, Immun & Canc, Paris, France
[2] Int Ctr Genet Engn & Biotechnol ICGEB, Cellular Immunol, Trieste, Italy
[3] INSERM, U1015, Gustave Roussy Canc Campus, Villejuif, France
[4] Univ Med Ctr Hamburg Eppendorf, Inst Biochem & Mol Cell Biol, Ctr Expt Med, Cell Commun & Migrat Lab, Hamburg, Germany
[5] PSL Res Univ, Inst Curie, CNRS, UMR144, Paris, France
[6] Malaghan Inst Med Res, Wellington, New Zealand
[7] Nantes Univ, Ctr Res Transplantat & Translat Immunol, INSERM, UMR 1064, Nantes, France
[8] Paris Cite Univ, Inst Curie, Immun & Canc, INSERM,U932, Paris, France
[9] Inst Curie, Platform NGS ICGEX, Paris, France
[10] Univ Toulouse III, Inst Toulousain Malad Infectieuses & Inflammatoire, INSERM, CNRS,UMR5051,UMR1291, Toulouse, France
[11] Natl Inst Hlth NIH, Natl Inst Environm Hlth Sci NIEHS, Immun Inflammat & Dis Lab, Res Triangle Pk, NC USA
[12] Univ Aix Marseille, Ctr Immunol Marseille Luminy, INSERM, CNRS, Marseille, France
[13] Kings Coll London, Ctr Inflammat Biol & Canc Immunol, Sch Immunol & Microbial Sci, London, England
[14] Xinxiang Med Univ, Sch Lab Med, Henan Key Lab Immunol & Targeted Therapy, Xinxiang, Peoples R China
[15] ASTAR, Singapore Immunol Network SIgN, 8A Biomed Grove, Singapore, Singapore
[16] Shanghai Jiao Tong Univ, Shanghai Inst Immunol, Sch Med, Dept Immunol & Microbiol, Shanghai, Peoples R China
[17] SingHealth Duke NUS Acad Med Ctr, Translat Immunol Inst, Singapore, Singapore
[18] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA USA
基金
欧盟地平线“2020”;
关键词
EXPRESSION; CCR7; GENERATION; MATURATION; TOLERANCE; IMMUNITY; TENSION; DAMAGE;
D O I
10.1038/s41590-024-01856-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 IKK beta-NF-kappa B-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. Dendritic cells experience cell shape changes while migrating within the complex physical environment of tissues. Sensing of these shape changes modifies their migratory properties and imprints these cells with immunoregulatory properties.
引用
收藏
页码:1193 / 1206
页数:33
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