Kaur Kawaljit, Safaie Tahmineh, Ko Meng-Wei, Wang Yuhao, Jewett Anahid
Division of Oral Biology and Oral Medicine, School of Dentistry and Medicine, Los Angeles, CA 90095, USA.
The Jonsson Comprehensive Cancer Center, UCLA School of Dentistry and Medicine, Los Angeles, CA 90095, USA.
Cancers (Basel). 2021 Jan 11;13(2):239. doi: 10.3390/cancers13020239.
Tumor cells are known to upregulate major histocompatibility complex-class I chain related proteins A and B (MICA/B) expression under stress conditions or due to radiation exposure. However, it is not clear whether there are specific stages of cellular maturation in which these ligands are upregulated or whether the natural killer (NK) cells differentially target these tumors in direct cytotoxicity or antibody-dependent cell cytotoxicity (ADCC). We used freshly isolated primary and osteoclast (OCs)-expanded NK cells to determine the degree of direct cytotoxicity or of ADCC using anti-MICA/B monoclonal antibodies (mAbs) against oral stem-like/poorly-differentiated oral squamous cancer stem cells (OSCSCs) and Mia PaCa-2 (MP2) pancreatic tumors as well as their well-differentiated counterparts: namely, oral squamous carcinoma cells (OSCCs) and pancreatic PL12 tumors. By using phenotypic and functional analysis, we demonstrated that OSCSCs and MP2 tumors were primary targets of direct cytotoxicity by freshly isolated NK cells and not by ADCC mediated by anti-MICA/B mAbs, which was likely due to the lower surface expression of MICA/B. However, the inverse was seen when their MICA/B-expressing differentiated counterparts, OSCCs and PL12 tumors, were used in direct cytotoxicity and ADCC, in which there was lower direct cytotoxicity but higher ADCC mediated by the NK cells. Differentiation of the OSCSCs and MP2 tumors by NK cell-supernatants abolished the direct killing of these tumors by the NK cells while enhancing NK cell-mediated ADCC due to the increased expression of MICA/B on the surface of these tumors. We further report that both direct killing and ADCC against MICA/B expressing tumors were significantly diminished by cancer patients' NK cells. Surprisingly, OC-expanded NK cells, unlike primary interleukin-2 (IL-2) activated NK cells, were found to kill OSCCs and PL12 tumors, and under these conditions, we did not observe significant ADCC using anti-MICA/B mAbs, even though the tumors expressed a higher surface expression of MICA/B. In addition, differentiated tumor cells also expressed higher levels of surface epidermal growth factor receptor (EGFR) and programmed death-ligand 1(PDL1) and were more susceptible to NK cell-mediated ADCC in the presence of anti-EGFR and anti-PDL1 mAbs compared to their stem-like/poorly differentiated counterparts. Overall, these results suggested the possibility of CD16 receptors mediating both direct cytotoxicity and ADCC, resulting in the competitive use of these receptors in either direct killing or ADCC, depending on the differentiation status of tumor cells and the stage of maturation and activation of NK cells.
已知肿瘤细胞在应激条件下或因辐射暴露会上调主要组织相容性复合体 I 类链相关蛋白 A 和 B(MICA/B)的表达。然而,尚不清楚这些配体是否在细胞成熟的特定阶段上调,也不清楚自然杀伤(NK)细胞在直接细胞毒性或抗体依赖性细胞毒性(ADCC)中是否对这些肿瘤有不同的靶向作用。我们使用新鲜分离的原代 NK 细胞和经破骨细胞(OCs)扩增的 NK 细胞,通过使用抗 MICA/B 单克隆抗体(mAb)来检测针对口腔干细胞样/低分化口腔鳞状癌干细胞(OSCSCs)和 Mia PaCa-2(MP2)胰腺肿瘤及其高分化对应物(即口腔鳞状癌细胞(OSCCs)和胰腺 PL12 肿瘤)的直接细胞毒性或 ADCC 程度。通过表型和功能分析,我们证明 OSCSCs 和 MP2 肿瘤是新鲜分离的 NK 细胞直接细胞毒性的主要靶点,而非抗 MICA/B mAb 介导的 ADCC 的靶点,这可能是由于 MICA/B 的表面表达较低。然而,当使用表达 MICA/B 的高分化对应物 OSCCs 和 PL12 肿瘤进行直接细胞毒性和 ADCC 时,情况则相反,即直接细胞毒性较低,但 NK 细胞介导的 ADCC 较高。NK 细胞上清液诱导 OSCSCs 和 MP2 肿瘤分化后,消除了 NK 细胞对这些肿瘤的直接杀伤作用,同时由于这些肿瘤表面 MICA/B 表达增加,增强了 NK 细胞介导的 ADCC。我们进一步报告,癌症患者的 NK 细胞对表达 MICA/B 的肿瘤的直接杀伤和 ADCC 均显著降低。令人惊讶的是,与原代白细胞介素 -2(IL-2)激活的 NK 细胞不同,并发现经 OC 扩增的 NK 细胞可杀伤 OSCCs 和 PL12 肿瘤,在这些条件下,即使肿瘤表面 MICA/B 表达较高,我们使用抗 MICA/B mAb 也未观察到显著的 ADCC。此外,与干细胞样/低分化对应物相比,分化的肿瘤细胞表面表皮生长因子受体(EGFR)和程序性死亡配体 1(PDL1)水平也更高,并且在存在抗 EGFR 和抗 PDL1 mAb 的情况下,对 NK 细胞介导的 ADCC 更敏感。总体而言,这些结果提示 CD16 受体介导直接细胞毒性和 ADCC 的可能性,导致这些受体在直接杀伤或 ADCC 中存在竞争性使用,这取决于肿瘤细胞的分化状态以及 NK 细胞的成熟和激活阶段。