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肿瘤坏死因子相关凋亡诱导配体在肝脏自然杀伤细胞监测肿瘤转移中的作用。

Involvement of tumor necrosis factor-related apoptosis-inducing ligand in surveillance of tumor metastasis by liver natural killer cells.

作者信息

Takeda K, Hayakawa Y, Smyth M J, Kayagaki N, Yamaguchi N, Kakuta S, Iwakura Y, Yagita H, Okumura K

机构信息

Department of Immunology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan.

出版信息

Nat Med. 2001 Jan;7(1):94-100. doi: 10.1038/83416.

Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induces apoptosis in various tumor cells in vitro, but its physiological role in tumor surveillance remains unknown. Here, we report that TRAIL is constitutively expressed on murine natural killer (NK) cells in the liver and plays a substantial role in suppressing tumor metastasis. Freshly isolated NK cells, but not natural killer T cells or ordinary T cells, from the liver expressed cell surface TRAIL, which was responsible for spontaneous cytotoxicity against TRAIL-sensitive tumor cells in vitro along with perforin and Fas ligand (FasL). Administration of neutralizing monoclonal antibody against TRAIL significantly increased experimental liver metastases of several TRAIL-sensitive tumor cell lines. Such an anti-metastatic effect of TRAIL was not observed in NK cell-depleted mice or interferon-gamma-deficient mice, the latter of which lacked TRAIL on liver NK cells. These findings provide the first evidence for the physiological function of TRAIL as a tumor suppressor.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)在体外可诱导多种肿瘤细胞凋亡,但其在肿瘤监测中的生理作用尚不清楚。在此,我们报告TRAIL在肝脏中的小鼠自然杀伤(NK)细胞上组成性表达,并在抑制肿瘤转移中发挥重要作用。从肝脏中新鲜分离的NK细胞而非自然杀伤T细胞或普通T细胞表达细胞表面TRAIL,其与穿孔素和Fas配体(FasL)一起负责体外对TRAIL敏感肿瘤细胞的自发细胞毒性。给予抗TRAIL中和单克隆抗体显著增加了几种TRAIL敏感肿瘤细胞系的实验性肝转移。在NK细胞耗竭的小鼠或干扰素γ缺陷小鼠中未观察到TRAIL的这种抗转移作用,后者肝脏NK细胞上缺乏TRAIL。这些发现为TRAIL作为肿瘤抑制因子的生理功能提供了首个证据。

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