Nature Communications (Feb 2024)

Cell softness renders cytotoxic T lymphocytes and T leukemic cells resistant to perforin-mediated killing

  • Yabo Zhou,
  • Dianheng Wang,
  • Li Zhou,
  • Nannan Zhou,
  • Zhenfeng Wang,
  • Jie Chen,
  • Ruiyang Pang,
  • Haixia Fu,
  • Qiusha Huang,
  • Fang Dong,
  • Hui Cheng,
  • Huafeng Zhang,
  • Ke Tang,
  • Jingwei Ma,
  • Jiadi Lv,
  • Tao Cheng,
  • Roland Fiskesund,
  • Xiaohui Zhang,
  • Bo Huang

DOI
https://doi.org/10.1038/s41467-024-45750-w
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract Mechanical force contributes to perforin pore formation at immune synapses, thus facilitating the cytotoxic T lymphocytes (CTL)-mediated killing of tumor cells in a unidirectional fashion. How such mechanical cues affect CTL evasion of perforin-mediated autolysis remains unclear. Here we show that activated CTLs use their softness to evade perforin-mediated autolysis, which, however, is shared by T leukemic cells to evade CTL killing. Downregulation of filamin A is identified to induce softness via ZAP70-mediated YAP Y357 phosphorylation and activation. Despite the requirements of YAP in both cell types for softness induction, CTLs are more resistant to YAP inhibitors than malignant T cells, potentially due to the higher expression of the drug-resistant transporter, MDR1, in CTLs. As a result, moderate inhibition of YAP stiffens malignant T cells but spares CTLs, thus allowing CTLs to cytolyze malignant cells without autolysis. Our findings thus hint a mechanical force-based immunotherapeutic strategy against T cell leukemia.