Abstract

T cells navigate diverse microenvironments to perform immune responses. Micro-scale topographical structures within the tissues, which may inherently exist in normal tissues or may be formed by inflammation or injury, can influence T cell migration, but how T cell migration is affected by such topographical structures have not been investigated. In this study, we fabricated ramp-like structures with a 5 μm height and various slopes, and observed T cells climbing up the ramp-like structures. T cells encountering the ramp-like structures exhibited MLC accumulation near head-tail junctions contacting the ramp-like structures, and made turns to the direction perpendicular to the ramp-like structures. Pharmacological study revealed that lamellipodia formation mediated by arp2/3 and contractility regulated by myosin light chain kinase (MLCK) were responsible for the intriguing turning behavior of T cells climbing the ramp-like structures. Arp2/3 or MLCK inhibition substantially reduced probability of T cells climbing sharp-edged ramp-like structures, indicating intriguing turning behavior of T cells mediated by lamellipodia formation and MLCK activity may be important for T cells to access inflamed or injured tissues with abrupt topographical changes.

Highlights

  • T cells are immune cells in adaptive immunity responsible for the initiation and orchestration of antigen-specific immune responses

  • Similar to previous experiments examining the effects of surface topography on T cell migration[22, 23, 25], poly(urethane acrylate) (PUA) ramp-like structures were coated with Intercellular Adhesion Molecule 1 (ICAM-1) to support the firm adhesion and migration of T cells

  • We investigated how T cells behave when they climb up the ramp-like structures with micron-scale topography

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Summary

Introduction

T cells are immune cells in adaptive immunity responsible for the initiation and orchestration of antigen-specific immune responses. Microfabricated surfaces presenting various topographical structures can be a powerful tool to investigate how surface topography regulates cell migration by allowing the independent control of surface topography and chemistry[20, 21]. Using this strategy, we fabricated periodic structures of nanoscale groove/ridge patterns[22, 23], which mimic the topography of extracellular matrixes (ECMs), or sinusoidal wavy structures with wavelengths of tens of micrometers[24, 25], which mimic www.nature.com/scientificreports/. The molecules responsible for this intriguing turning behavior were further identified and characterized by pharmacological inhibitors and fluorescence live-cell imaging

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