Emerging functions of cytoskeletal proteins in immune diseases

Immune cells are especially dependent on the proper functioning of the actin cytoskeleton, and both innate and adaptive responses rely on it. Leukocytes need to adhere not only to substrates but also to cells in order to form synapses that pass on instructions or kill infected cells. Neutrophils literally squeeze their cell body during blood extravasation and efficiently migrate to the inflammatory focus. Moreover, the development of immune cells requires the remodeling of their cytoskeleton as it depends on, among other processes, adhesive contacts and migration. In recent years, the number of reports describing cytoskeletal defects that compromise the immune system has increased immensely. Furthermore, a new emerging paradigm points toward a role for the cellular actin content as an essential component of the so-called homeostasis-alteringmolecular processes that induce the activation of innate immune signaling pathways. Here, we review the role of critical actin-cytoskeleton-remodeling proteins, including the Arp2/3 complex, cofilin, coronin and WD40-repeat containing protein 1 (WDR1), in immune pathophysiology, with a special focus on autoimmune and autoinflammatory traits.

Automated summary

Immune cells heavily rely on the proper functioning of the actin cytoskeleton for various functions like adhesion, migration, and synapse formation. Dysfunctions in the cytoskeleton can compromise immune responses and lead to immune system defects. Recent research has highlighted the importance of actin-cytoskeleton-remodeling proteins in immune pathophysiology, particularly in autoimmune and autoinflammatory conditions.