American Physical Society March Meeting, California, Amerika Birleşik Devletleri, 07 Mart 2018, ss.1
T lymphocytes are an integral
part of the adaptive immune response. The detection of infectious agents critically depends
on the interaction of T cells
with antigen presenting cells, which have varying mechanical stiffness and complex topological features.
It has been recently
recognized that T cell
activation is regulated both by
stiffness of the antigen presenting surface and by cytoskeletal forces which partially arise from actomyosin contractility. However, the relationship between stiffness and the force generating machinery
driving T cell activation is not well understood. To address this problem, we characterized actin and myosin dynamics during
the activation of Jurkat T
cells on stimulatory elastic substrates with variable
stiffness using total internal reflection fluorescence (TIRF) and confocal microscopy. Activated T cells exhibit lamellipodial actin and myosin flows at the
cell periphery as well as lamellar rings of actomyosin bundles.
We have explored the stiffness-dependent organization of these distinct
actomyosin structures and flows and their correlation with the spatiotemporal variation of traction
stresses. This study provides insight
into the potential role of stiffness
in regulating cytoskeletal organization and force generation during T cell activation.