Sign in

Abstract

Interacting, self-propelled particles are prone to jamming when crowded. This well-described phenomenon is shared by diverse systems including cars, animal colonies, and pedestrians. T cells, essential effectors of adaptive immunity, seemingly defy this principle: the rapid migration enabling their protective function persists even in tightly packed tissue environments - from the thymus where T cells develop, to lymphoid organs they survey for antigen, to tissues they clear from infection. Here we studied T cell crowds by combining experiments of T cells migrating in microfluidic devices with in silico models. We observed that while single T cells are highly heterogeneous in their motility, in crowds they synchronized their speeds and formed stable, motile trains. Our models showed that the emergence of this flocking-like behavior can be explained by a combination of two interaction mechanisms at the cell-cell interface: adhesion maintains cohesive T cell groups, and force transmission accelerates slower cells. Not all immune cells flock when they are crowded: neutrophils in the same settings slowed down with increasing cell density. Thus, cooperative motion may enable T cells to remain motile in densely packed tissue environments, preventing jams that curtail the motion of other crowded systems.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.