Different TCR-induced T lymphocyte responses are potentiated by stiffness with variable sensitivity

Author:

Saitakis Michael1,Dogniaux Stéphanie1,Goudot Christel1,Bufi Nathalie2,Asnacios Sophie23,Maurin Mathieu1,Randriamampita Clotilde4,Asnacios Atef2,Hivroz Claire1ORCID

Affiliation:

1. Institut Curie Section Recherche, INSERM U932 & PSL Research University, Paris, France

2. Laboratoire Matières et systèmes complexes, Université Paris-Diderot and CNRS, UMR 7057, Sorbonne Paris Cité, Paris, France

3. Department of Physics, Sorbonne Universités, UPMC Université Paris, Paris, France

4. INSERM, U1016, Institut Cochin & UMR8104, CNRS & Université Paris Descartes, Sorbonne Paris Cité, Paris, France

Abstract

T cells are mechanosensitive but the effect of stiffness on their functions is still debated. We characterize herein how human primary CD4+ T cell functions are affected by stiffness within the physiological Young’s modulus range of 0.5 kPa to 100 kPa. Stiffness modulates T lymphocyte migration and morphological changes induced by TCR/CD3 triggering. Stiffness also increases TCR-induced immune system, metabolism and cell-cycle-related genes. Yet, upon TCR/CD3 stimulation, while cytokine production increases within a wide range of stiffness, from hundreds of Pa to hundreds of kPa, T cell metabolic properties and cell cycle progression are only increased by the highest stiffness tested (100 kPa). Finally, mechanical properties of adherent antigen-presenting cells modulate cytokine production by T cells. Together, these results reveal that T cells discriminate between the wide range of stiffness values found in the body and adapt their responses accordingly.

Funder

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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