Immune cells turn into ’Mini-Hulks’ to push away tissue and make space when migrating

"Eww; what, inside of me?" A common response when Patricia Reis-Rodrigues, a PhD candidate in the Sixt group at ISTA , reveals that dendritic cells-a type of immune cell-are constantly moving throughout our bodies. Dendritic cells can be found in the peripheral tissues, like the skin, where they scan for intruders such as bacteria or viruses. When they encounter such pathogens, dendritic cells get activated and migrate from the infection site to the lymph nodes, where they interact with T cells to start the fight against the infection.
Effective immune responses rely on the efficient and coordinated movement of dendritic cells throughout our body. However, navigating three-dimensional tissues can be complex and unpredictable, and cells need to make use of their organelles and cytoskeleton in different ways to overcome the obstacles that surround them.
Navigating through complex environments
But what happens when cells face constricted spaces that are too small to allow free passage? While fibroblasts (cells involved in tissue repair) or cancer cells often secrete proteolytic enzymes that digest their environment to make room, dendritic cells use a different technique. "If our dendritic cells did that, they would eat away too much of our tissue, which would be very bad. You would be quite holey," Reis-Rodrigues chuckles.
Reis-Rodrigues and colleagues’ newest paper, which was just published in Nature Immunology, shows that, when confronted with tight spaces, dendritic cells assemble a distinct actin structure at the center of the cell body. This central actin structure can push the surrounding obstacles away, orthogonally to the direction of movement, generating space for the cells and helping them overcome even the tightest holes. The success of this strategy relies heavily on the coordination between these outward pushing forces at the center of the cell, and the forces at the front that form the lamellipodium and promote forward migration.
Unable to push, cells get trapped and entangled
"There was no clear understanding of why a mutation in this gene would impact our cells so significantly and lead to the development of such severe symptoms in people," Reis-Rodrigues explains. The team demonstrated that unlike healthy immune cells, the inability of DOCK8 mutants to push outwards and open up narrow environments trapped the cell body in tight holes. The lack of the central actin structure also led to extensive uncontrolled protrusions at the front, elongating cells so much that they even fragmented and died.
Publication:
P. Reis-Rodrigues, M. J. Avellaneda, N. Canigova, F. Gaertner, K. Vaahtomeri, M. Riedl, I. de Vries, J. Merrin, R. Hauschild, Y. Fukui, A. Juanes Garcia & M. Sixt. 2025. Migrating immune cells globally coordinate protrusive forces. Nature Immunology. DOI: 10.1038/s41590-025-02211-w
