these observations do not suggest 
that the cells arrive at the same final state with and without myosin, as detailed below. Rather, it reveals that the large scale spatial organization of the IS probably offers insufficient information from which to judge the more subtle internal state of the cell. Forces applied to TCR clusters are translated to myosin IIA myosin IIA at earlier times is significantly reduced. By performing the same experiments on actin, we also observed that actin retrograde flow decreases on the patterned lipid bilayers consistently with myosin. The slow-down of myosin in response to physically constrained TCRs confirms the existence of a mechanical coupling between TCR and myosin. Moreover, because contractile forces in actin are generated by myosin and studies have shown that resistive load on non-muscle myosin IIA leads to its slower power stokes on actin, the reduced actin retrograde flow on pattern lipid bilayers points to actin cytoskeleton as responsible for transmitting the resisting force from TCR microclusters to myosin. Myosin IIA is required for Ca2+ influx A hallmark of T cell activation downstream of TCR signaling is the elevation of intracellular calcium, which in turn activates a number of calcium-dependent pathways. We used Fura-2 as the indicator of intracellular calcium concentration; the ratio of its emission intensities at 340 nm excitation versus 380 nm is proportional to Ca2+ concentration. In control cells, intracellular Ca2+ concentration rapidly increases within 1 min after the R-547 site initial Myosin IIA in Immunological Synapse Formation cell-bilayer contact. By contrast, cells pretreated with ML-7 do not show any significant Ca2+ elevation, but maintain a low Ca2+ level similar to baseline. The Ca2+ concentration traces of a large population of both control cells and cells pretreated with ML-7 show a dramatic reduction in the calcium influx in response to myosin IIA inhibition. In agreement with previous work on Jurkat cells, the results show that myosin IIA is important for calcium signaling in primary T cells. in T cells fixed at both 1.5 min and 5 min after stimulation, but not at 45 sec. The phosphorylation level of ZAP-70 at the IS also decreases in the absence of myosin function. Myosin IIA therefore contributes to the stable association of active ZAP-70 with TCR, but it is not necessary for the initial recruitment. Inhibition of myosin IIA reduces CasL phosphorylation To our knowledge, there have been no previous studies directly quantifying the cytoskeletal strain in T cells and correlating this to TCR signaling. The data we report above and other published results clearly indicate at least an indirect influence of myosin IIA on TCR signaling, but the role of its mechanical forces in the process still remains unclear. To explore that question we studied the phosphorylation of CasL. It is a member of the mechanosensing Cas protein family and is predominately expressed in T lymphocytes. All Cas family proteins contain a highly conserved Src kinase substrate domain, which is consisted of PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22183349 multiple Tyr-x-x-Pro motifs. Studies on p130Cas, one of the Cas proteins, have shown that mechanical stretching changes conformation of the motifs and leads to enhancement of tyrosine phosphorylation and possibly downstream signaling. Whether or not CasL is involved in molecular force transduction is less clear, but its phosphorylation level strongly depends on actin integrity in several cell types, suggesting
