Basu Roshni, Whitlock Benjamin M, Husson Julien, Le Floc'h Audrey, Jin Weiyang, Oyler-Yaniv Alon, Dotiwala Farokh, Giannone Gregory, Hivroz Claire, Biais Nicolas, Lieberman Judy, Kam Lance C, Huse Morgan
Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Biochemistry and Molecular Biology Graduate Program, Weill-Cornell Medical College, New York, NY 10065, USA.
Cell. 2016 Mar 24;165(1):100-110. doi: 10.1016/j.cell.2016.01.021. Epub 2016 Feb 25.
The immunological synapse formed between a cytotoxic T lymphocyte (CTL) and an infected or transformed target cell is a physically active structure capable of exerting mechanical force. Here, we investigated whether synaptic forces promote the destruction of target cells. CTLs kill by secreting toxic proteases and the pore forming protein perforin into the synapse. Biophysical experiments revealed a striking correlation between the magnitude of force exertion across the synapse and the speed of perforin pore formation on the target cell, implying that force potentiates cytotoxicity by enhancing perforin activity. Consistent with this interpretation, we found that increasing target cell tension augmented pore formation by perforin and killing by CTLs. Our data also indicate that CTLs coordinate perforin release and force exertion in space and time. These results reveal an unappreciated physical dimension to lymphocyte function and demonstrate that cells use mechanical forces to control the activity of outgoing chemical signals.
细胞毒性T淋巴细胞(CTL)与受感染或转化的靶细胞之间形成的免疫突触是一种能够施加机械力的物理活性结构。在此,我们研究了突触力是否会促进靶细胞的破坏。CTL通过向突触中分泌有毒蛋白酶和形成孔道的蛋白穿孔素来杀伤细胞。生物物理实验揭示了突触间施加力的大小与靶细胞上穿孔素孔形成速度之间存在显著相关性,这意味着力通过增强穿孔素活性来增强细胞毒性。与这一解释一致,我们发现增加靶细胞张力会增强穿孔素形成孔道的能力以及CTL的杀伤作用。我们的数据还表明,CTL在空间和时间上协调穿孔素释放和力的施加。这些结果揭示了淋巴细胞功能中一个未被重视的物理维度,并证明细胞利用机械力来控制传出化学信号的活性。