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细胞形状感知使树突状细胞能够进行稳态迁移到淋巴结。

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

机构信息

INSERM U932, Immunity and Cancer, Institut Curie, PSL University, Paris, France.

Cellular Immunology, International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.

出版信息

Nat Immunol. 2024 Jul;25(7):1193-1206. doi: 10.1038/s41590-024-01856-3. Epub 2024 Jun 4.

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 cPLA, 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.

摘要

免疫细胞在环境巡逻时会经历较大的细胞形状变化,这是由于它们在组织中迁移时遇到的物理限制。这些细胞可以使用专门的形状感应途径来适应这种变形事件。然而,形状感应如何影响免疫细胞的功能在很大程度上是未知的。在这里,我们确定了一种形状感应机制,该机制增加了趋化因子受体 CCR7 的表达,并指导树突状细胞在稳态下从外周组织迁移到淋巴结。这种机制依赖于脂质代谢酶 cPLA,需要核包膜张力,并由 ARP2/3 肌动蛋白成核复合物精细调节。我们还表明,这种形状感应轴通过激活 IKKβ-NF-κB 依赖性途径来重新编程树突状细胞转录,该途径已知可控制其耐受潜力。这些结果表明,免疫细胞经历的细胞形状变化可以决定它们的迁移行为和免疫调节特性,并揭示了组织的物理特性对适应性免疫的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a4c/11224020/b77f24c0ac2f/41590_2024_1856_Fig1_HTML.jpg

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