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肿瘤发展过程中肿瘤浸润淋巴细胞中自然杀伤细胞的早期出现与激活。

Early appearance and activation of natural killer cells in tumor-infiltrating lymphoid cells during tumor development.

作者信息

Kurosawa S, Matsuzaki G, Harada M, Ando T, Nomoto K

机构信息

Department of Immunology, Kyushu University, Fukuoka, Japan.

出版信息

Eur J Immunol. 1993 May;23(5):1029-33. doi: 10.1002/eji.1830230507.

Abstract

We investigated NK cell infiltration into tumor developing lesions at early stage of tumor development after intraperitoneal inoculation of 3LL lung carcinoma into syngeneic C57BL/6 mice. Natural killer (NK) cells, which were detected by anti-NK 1.1 monoclonal antibody (mAb), remarkably increased in number in tumor-developing lesions (peritoneal cavity) as early as day 3 after inoculation of 3LL. The tumor-infiltrating NK cells from 3LL-inoculated mice produced a high level of interferon-gamma by co-culture with 3LL and showed enhanced cytotoxic activities against both NK-sensitive (YAC-1) and NK-resistant (3LL and P815) tumors. Furthermore, mice depleted of NK cells by injection of anti-NK 1.1 mAb or anti-asialo GM1 antibody showed shorter survival times after intraperitoneal inoculation of 3LL when compared with control mice. These results suggest that NK cells infiltrate the tumor-developing lesion at an early stage and may participate in the early protection against tumors through production of a high amount of interferon-gamma and enhanced cytotoxicity at tumor-bearing sites.

摘要

我们将3LL肺癌腹腔接种到同基因C57BL/6小鼠体内,研究了肿瘤发生早期阶段自然杀伤(NK)细胞向肿瘤发生病变部位的浸润情况。用抗NK 1.1单克隆抗体(mAb)检测到的NK细胞,早在接种3LL后第3天,肿瘤发生病变部位(腹腔)的数量就显著增加。来自接种3LL小鼠的肿瘤浸润NK细胞与3LL共培养时产生高水平的γ干扰素,并对NK敏感(YAC-1)和NK抗性(3LL和P815)肿瘤均表现出增强的细胞毒性活性。此外,与对照小鼠相比,注射抗NK 1.1 mAb或抗去唾液酸GM1抗体使NK细胞耗竭的小鼠在腹腔接种3LL后存活时间更短。这些结果表明,NK细胞在早期浸润肿瘤发生病变部位,并可能通过在荷瘤部位产生大量γ干扰素和增强细胞毒性来参与早期抗肿瘤保护。

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