MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Headley Way, Oxford OX3 9DS, UK.
Koch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA
J Cell Sci. 2019 Sep 4;133(5):jcs232322. doi: 10.1242/jcs.232322.
Cytoskeletal actin dynamics are crucial for the activation of T-cells. Immortalised Jurkat T-cells have been the model system of choice to examine and correlate the dynamics of the actin cytoskeleton and the immunological synapse leading to T-cell activation. However, it has remained unclear whether immortalised cellular systems, such as Jurkat T-cells can recapitulate the cytoskeletal behaviour of primary T-cells. Studies delineating the cytoskeletal behaviour of Jurkat T-cells in comparison to primary T-cells are lacking. Here, we employ live-cell super-resolution microscopy to investigate the cytoskeletal actin organisation and dynamics of living primary and immortalised Jurkat T-cells at the appropriate spatiotemporal resolution. Under comparable activation conditions, we found differences in the architectural organisation and dynamics of Jurkat and primary mouse and human T-cells. Although the three main actin network architectures in Jurkat T-cells were reminiscent of primary T-cells, there were differences in the organisation and molecular mechanisms underlying these networks. Our results highlight mechanistic distinctions in the T-cell model system most utilised to study cytoskeletal actin dynamics.
细胞骨架肌动蛋白动力学对于 T 细胞的激活至关重要。永生 Jurkat T 细胞一直是选择的模型系统,用于检查和关联肌动蛋白细胞骨架和免疫突触的动力学,从而导致 T 细胞激活。然而,仍然不清楚永生细胞系统(如 Jurkat T 细胞)是否可以再现原代 T 细胞的细胞骨架行为。缺乏描绘 Jurkat T 细胞与原代 T 细胞相比的细胞骨架行为的研究。在这里,我们采用活细胞超分辨率显微镜,以适当的时空分辨率研究活的原代和永生 Jurkat T 细胞的细胞骨架肌动蛋白组织和动力学。在可比较的激活条件下,我们发现 Jurkat 和原代小鼠和人类 T 细胞在结构组织和动力学方面存在差异。尽管 Jurkat T 细胞中的三种主要肌动蛋白网络结构类似于原代 T 细胞,但这些网络的组织和分子机制存在差异。我们的结果强调了最常用于研究细胞骨架肌动蛋白动力学的 T 细胞模型系统中的机制区别。