Ca²⁺ microdomains and spatially resolved Ca²⁺ signals are highly relevant for cell function. In T cells, local Ca²⁺ signaling at the immunological synapse (IS) is required for downstream effector functions. We present experimental evidence that the relocation of the MTOC towards the IS during polarization drags mitochondria along with the microtubule network. From time-lapse fluorescence microscopy we conclude that mitochondria rotate together with the cytoskeleton towards the IS. We hypothesize that this movement of mitochondria towards the IS together with their functionality of absorption and spatial redistribution of Ca²⁺ is sufficient to significantly increase the cytosolic Ca²⁺ concentration. To test this hypothesis we developed a whole cell model for Ca²⁺ homoeostasis involving specific geometries for mitochondria and use the model to calculate the spatial distribution of Ca²⁺ concentrations within the cell body as a function of the rotation angle and the distance from the IS. We find that an inhomogeneous distribution of PMCA pumps on the cell membrane, in particular an accumulation of PMCA at the IS, increases the global Ca²⁺ concentration and decreases the local Ca²⁺ concentration at the IS with decreasing distance of the MTOC from the IS. Unexpectedly, a change of CRAC/Orai activity is not required to explain the observed Ca²⁺ changes. We conclude that rotation-driven relocation of the MTOC towards the IS together with an accumulation of PMCA pumps at the IS are sufficient to control the observed Ca²⁺ dynamics in T-cells during polarization.