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T-cell activation is modulated by the 3D mechanical microenvironment.


ABSTRACT: T cells recognize mechanical forces through a variety of cellular pathways, including mechanical triggering of both the T-cell receptor (TCR) and integrin LFA-1. Here we show that T cells can recognize forces arising from the mechanical rigidity of the microenvironment. We fabricated 3D scaffold matrices with mechanical stiffness tuned to the range 4-40 kPa and engineered them to be microporous, independently of stiffness. We cultured T cells and antigen presenting cells within the matrices and studied T-cell activation by flow cytometry and live-cell imaging. We found that there was an augmentation of T-cell activation, proliferation, and migration speed in the context of mechanically stiffer 3D matrices as compared to softer materials. These results show that T cells can sense their 3D mechanical environment and alter both their potential for activation and their effector responses in different mechanical environments. A 3D scaffold of tunable stiffness and consistent microporosity offers a biomaterial advancement for both translational applications and reductionist studies on the impact of tissue microenvironmental factors on cellular behavior.

SUBMITTER: Majedi FS 

PROVIDER: S-EPMC7307918 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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T-cell activation is modulated by the 3D mechanical microenvironment.

Majedi Fatemeh S FS   Hasani-Sadrabadi Mohammad Mahdi MM   Thauland Timothy J TJ   Li Song S   Bouchard Louis-S LS   Butte Manish J MJ  

Biomaterials 20200424


T cells recognize mechanical forces through a variety of cellular pathways, including mechanical triggering of both the T-cell receptor (TCR) and integrin LFA-1. Here we show that T cells can recognize forces arising from the mechanical rigidity of the microenvironment. We fabricated 3D scaffold matrices with mechanical stiffness tuned to the range 4-40 kPa and engineered them to be microporous, independently of stiffness. We cultured T cells and antigen presenting cells within the matrices and  ...[more]

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