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Soft Polydimethylsiloxane-Supported Lipid Bilayers for Studying T Cell Interactions

Much of what we know about the early stages of T cell activation has been obtained from studies of T cells interacting with glass-supported lipid bilayers that favor imaging but are orders of magnitude stiffer than typical cells. We developed a method for attaching lipid bilayers to polydimethylsilo...

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Detalles Bibliográficos
Autores principales: Lippert, Anna H., Dimov, Ivan B., Winkel, Alexander K., Humphrey, Jane, McColl, James, Chen, Kevin Y., Santos, Ana M., Jenkins, Edward, Franze, Kristian, Davis, Simon J., Klenerman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820804/
https://www.ncbi.nlm.nih.gov/pubmed/33248128
http://dx.doi.org/10.1016/j.bpj.2020.11.021
Descripción
Sumario:Much of what we know about the early stages of T cell activation has been obtained from studies of T cells interacting with glass-supported lipid bilayers that favor imaging but are orders of magnitude stiffer than typical cells. We developed a method for attaching lipid bilayers to polydimethylsiloxane polymer supports, producing “soft bilayers” with physiological levels of mechanical resistance (Young’s modulus of 4 kPa). Comparisons of T cell behavior on soft and glass-supported bilayers revealed that whereas late stages of T cell activation are thought to be substrate-stiffness dependent, early calcium signaling was unaffected by substrate rigidity, implying that early steps in T cell receptor triggering are not mechanosensitive. The exclusion of large receptor-type phosphatases was observed on the soft bilayers, however, even though it is yet to be demonstrated at authentic cell-cell contacts. This work sets the stage for an imaging-based exploration of receptor signaling under conditions closely mimicking physiological cell-cell contact.