Sakuma Mei, Katagata Masanori, Okayama Hirokazu, Nakajima Shotaro, Saito Katsuharu, Sato Takahiro, Fukai Satoshi, Tsumuraya Hideaki, Onozawa Hisashi, Sakamoto Wataru, Saito Motonobu, Saze Zenichiro, Momma Tomoyuki, Mimura Kosaku, Kono Koji
Department of Gastrointestinal Tract Surgery, Fukushima Medical University, Fukushima 960-1295, Japan.
Department of Multidisciplinary Treatment of Cancer and Regional Medical Support, Fukushima Medical University, Fukushima 960-1295, Japan.
Cancers (Basel). 2024 May 15;16(10):1888. doi: 10.3390/cancers16101888.
TIM-3 was originally identified as a negative regulator of helper T cells and is expressed on dendritic cells (DCs). Since the inhibition of TIM-3 on DCs has been suggested to enhance T cell-mediated anti-tumor immunity, we examined its expression on DCs within the tumor microenvironment (TME) in colorectal cancer (CRC) using transcriptomic data from a public database ( = 592) and immunohistochemical evaluations from our cohorts of CRC ( = 115). The expression of TIM-3 on DCs in vitro was examined by flow cytometry, while the expression of its related molecules, cGAS and STING, on immature and mature DCs was assessed by Western blotting. The expression of (TIM-3) was strongly associated with the infiltration of DCs within the TME of CRC. Immunohistochemical staining of clinical tissue samples revealed that tumor-infiltrating DCs expressed TIM-3; however, their number at the tumor-invasive front significantly decreased with stage progression. TIM-3 expression was higher on immature DCs than on mature DCs from several different donors ( = 6). Western blot analyses showed that the expression of STING was higher on mature DCs than on immature DCs, which was opposite to that of TIM-3. We demonstrated that TIM-3 was highly expressed on tumor-infiltrating DCs of CRC and that its expression was higher on immature DCs than on mature DCs.
TIM-3最初被鉴定为辅助性T细胞的负调节因子,并在树突状细胞(DC)上表达。由于已有研究表明抑制DC上的TIM-3可增强T细胞介导的抗肿瘤免疫,我们利用公共数据库中的转录组数据(n = 592)以及我们的结直肠癌(CRC)队列的免疫组织化学评估,检测了其在CRC肿瘤微环境(TME)中DC上的表达。通过流式细胞术检测体外DC上TIM-3的表达,同时通过蛋白质免疫印迹法评估其相关分子cGAS和STING在未成熟和成熟DC上的表达。TIM-3的表达与CRC的TME中DC的浸润密切相关。临床组织样本的免疫组织化学染色显示,肿瘤浸润性DC表达TIM-3;然而,随着分期进展,它们在肿瘤侵袭前沿的数量显著减少。来自几个不同供体(n = 6)的未成熟DC上TIM-3的表达高于成熟DC。蛋白质免疫印迹分析显示,成熟DC上STING的表达高于未成熟DC,这与TIM-3的情况相反。我们证明,TIM-3在CRC的肿瘤浸润性DC上高表达,且其在未成熟DC上的表达高于成熟DC。