During T cell activation, the engagement of a T cell with an antigen-presenting cell (APC) results in rapid cytoskeletal rearrangements and a dramatic increase of intracellular calcium (Ca 2+ ) concentration, downstream to T cell antigen receptor (TCR) ligation. These events facilitate the organization of an immunological synapse (IS), which supports the redistribution of receptors, signaling molecules and organelles towards the T cell–APC interface to induce downstream signaling events, ultimately supporting T cell effector functions. Thus, Ca 2+ signaling and cytoskeleton rearrangements are essential for T cell activation and T cell-dependent immune response. Rapid release of Ca 2+ from intracellular stores, e.g. the endoplasmic reticulum (ER), triggers the opening of Ca 2+ release-activated Ca 2+ (CRAC) channels, residing in the plasma membrane. These channels facilitate a sustained influx of extracellular Ca 2+ across the plasma membrane in a process termed store-operated Ca 2+ entry (SOCE). Because CRAC channels are themselves inhibited by Ca 2+ ions, additional factors are suggested to enable the sustained Ca 2+ influx required for T cell function. Among these factors, we focus here on the contribution of the actin and microtubule cytoskeleton. The TCR-mediated increase in intracellular Ca 2+ evokes a rapid cytoskeleton-dependent polarization, which involves actin cytoskeleton rearrangements and microtubule-organizing center (MTOC) reorientation. Here, we review the molecular mechanisms of Ca 2+ flux and cytoskeletal rearrangements, and further describe the way by which the cytoskeletal networks feedback to Ca 2+ signaling by controlling the spatial and temporal distribution of Ca 2+ sources and sinks, modulating TCR-dependent Ca 2+ signals, which are required for an appropriate T cell response. This article is part of a Special Issue entitled: Reciprocal influences between cell cytoskeleton and membrane channels, receptors and transporters. Guest Editor: Jean Claude Hervé.