Cell shape sensing licenses dendritic cells for homeostatic migration to lymph nodes.
Zahraa AlraiesClaudia A RiveraMaria-Graciela DelgadoDoriane SanséauMathieu MaurinRoberto AmadioGiulia Maria PipernoGarett DunsmoreAline YatimLivia Lacerda MarianoAnna KniazevaVincent CalmettesPablo J SáezAlice WilliartHenri PopardMatthieu GratiaOlivier LamiableAurélie MoreauZoé FusilierLou CresteyBenoit AlbaudPatricia LegoixAnne S DejeanAnne-Louise Le DorzeHideki NakanoDonald N CookToby LawrenceNicolas ManelFederica BenvenutiFlorent GinhouxHélène D MoreauGuilherme P F NaderMatthieu PielAna-Maria Lennon-DuménilPublished in: Nature immunology (2024)
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 cPLA 2 , 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.
Keyphrases
- dendritic cells
- lymph node
- single cell
- cell migration
- regulatory t cells
- gene expression
- immune response
- signaling pathway
- cell therapy
- physical activity
- mental health
- oxidative stress
- induced apoptosis
- lps induced
- inflammatory response
- bone marrow
- dna methylation
- transcription factor
- toll like receptor
- endoplasmic reticulum stress
- nuclear factor