Efficient homing of T cells via afferent lymphatics requires mechanical arrest and integrin-supported chemokine guidance

T细胞通过传入淋巴管高效归巢需要机械阻滞和整合素支持的趋化因子引导。

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作者:Rieke Martens # ,Marc Permanyer # ,Kathrin Werth # ,Kai Yu # ,Asolina Braun ,Olga Halle ,Stephan Halle ,Gwendolyn E Patzer ,Berislav Bošnjak ,Friedemann Kiefer ,Anika Janssen ,Michaela Friedrichsen ,Jenny Poetzsch ,Karan Kohli ,Yvonne Lueder ,Rodrigo Gutierrez Jauregui ,Nadine Eckert ,Tim Worbs ,Melanie Galla ,Reinhold Förster

Abstract

Little is known regarding lymph node (LN)-homing of immune cells via afferent lymphatics. Here, we show, using a photo-convertible Dendra-2 reporter, that recently activated CD4 T cells enter downstream LNs via afferent lymphatics at high frequencies. Intra-lymphatic immune cell transfer and live imaging data further show that activated T cells come to an instantaneous arrest mediated passively by the mechanical 3D-sieve barrier of the LN subcapsular sinus (SCS). Arrested T cells subsequently migrate randomly on the sinus floor independent of both chemokines and integrins. However, chemokine receptors are imperative for guiding cells out of the SCS, and for their subsequent directional translocation towards the T cell zone. By contrast, integrins are dispensable for LN homing, yet still contribute by increasing the dwell time within the SCS and by potentially enhancing T cell sensing of chemokine gradients. Together, these findings provide fundamental insights into mechanisms that control homing of lymph-derived immune cells.

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