Cytoskeleton and Cancer Progression, Department of Cancer Research, Luxembourg Institute of Health, Luxembourg, Luxembourg.
Faculty of Science, Technology and Medicine University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Front Immunol. 2023 Oct 5;14:1276602. doi: 10.3389/fimmu.2023.1276602. eCollection 2023.
Cytotoxic lymphocytes (CLs), specifically cytotoxic T lymphocytes and natural killer cells, are indispensable guardians of the immune system and orchestrate the recognition and elimination of cancer cells. Upon encountering a cancer cell, CLs establish a specialized cellular junction, known as the immunological synapse that stands as a pivotal determinant for effective cell killing. Extensive research has focused on the presynaptic side of the immunological synapse and elucidated the multiple functions of the CL actin cytoskeleton in synapse formation, organization, regulatory signaling, and lytic activity. In contrast, the postsynaptic (cancer cell) counterpart has remained relatively unexplored. Nevertheless, both indirect and direct evidence has begun to illuminate the significant and profound consequences of cytoskeletal changes within cancer cells on the outcome of the lytic immunological synapse. Here, we explore the understudied role of the cancer cell actin cytoskeleton in modulating the immune response within the immunological synapse. We shed light on the intricate interplay between actin dynamics and the evasion mechanisms employed by cancer cells, thus providing potential routes for future research and envisioning therapeutic interventions targeting the postsynaptic side of the immunological synapse in the realm of cancer immunotherapy. This review article highlights the importance of actin dynamics within the immunological synapse between cytotoxic lymphocytes and cancer cells focusing on the less-explored postsynaptic side of the synapse. It presents emerging evidence that actin dynamics in cancer cells can critically influence the outcome of cytotoxic lymphocyte interactions with cancer cells.
细胞毒性淋巴细胞 (CLs),特别是细胞毒性 T 淋巴细胞和自然杀伤细胞,是免疫系统不可或缺的守护者,它们协调识别和消除癌细胞。当遇到癌细胞时,CLs 会建立一个专门的细胞连接,称为免疫突触,它是有效细胞杀伤的关键决定因素。大量研究集中在免疫突触的前突触侧,并阐明了 CL 肌动蛋白细胞骨架在突触形成、组织、调节信号和裂解活性中的多种功能。相比之下,后突触(癌细胞)对应物仍然相对未被探索。尽管如此,间接和直接证据已经开始阐明癌细胞骨架变化对裂解免疫突触结果的重大而深远的影响。在这里,我们探讨了癌细胞肌动蛋白细胞骨架在调节免疫突触内免疫反应中的作用。我们揭示了肌动蛋白动力学与癌细胞逃避机制之间的复杂相互作用,从而为未来的研究提供了潜在途径,并设想了针对癌症免疫治疗中免疫突触后突触侧的治疗干预措施。这篇综述文章强调了细胞毒性淋巴细胞和癌细胞之间免疫突触中肌动蛋白动力学的重要性,重点关注突触后侧这一研究较少的领域。它提出了新的证据,表明癌细胞中的肌动蛋白动力学可以严重影响细胞毒性淋巴细胞与癌细胞相互作用的结果。