Microtubules restrict F-actin polymerization to the immune synapse via GEF-H1 to maintain polarity in lymphocytes

Judith Pineau (1) , Léa Pinon (1) , Olivier Mesdjian (2) , Jacques Fattaccioli (2) , Ana-Maria Lennon Duménil , Paolo Pierobon (3, 1)

1 Centre de recherche de l'Institut Curie [Paris]
2 Département de Chimie - ENS Paris
3 U932 - Immunité et cancer

Immune synapse formation is a key step for lymphocyte activation. In B lymphocytes, the immune synapse controls the production of high-affinity antibodies, thereby defining the efficiency of humoral immune responses. While the key roles played by both the actin and microtubule cytoskeletons in the formation and function of the immune synapse have become increasingly clear, how the different events involved in synapse formation are coordinated in space and time by actin-microtubule interactions is not understood. Using a microfluidic pairing device, we studied with unprecedented resolution the dynamics of the various events leading to immune synapse formation and maintenance. Our results identify two groups of events, local and global dominated by actin and microtubules dynamics, respectively. They further highlight an unexpected role for microtubules and the GEF-H1-RhoA axis in restricting F-actin polymerization at the immune synapse to define the cell polarity axis, allowing the formation and maintenance of a unique competent immune synapse.

Domaines: Organisation et fonctions cellulaires [q-bio.SC]; Biophysique [physics.bio-ph]; Biophysique

Judith Pineau, Léa Pinon, Olivier Mesdjian, Jacques Fattaccioli, Ana-Maria Lennon Duménil, et al.. Microtubules restrict F-actin polymerization to the immune synapse via GEF-H1 to maintain polarity in lymphocytes. eLife, 2022, 11, ⟨10.1101/2022.01.03.473915⟩. ⟨hal-03853508⟩