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转染到中国仓鼠卵巢细胞中的白细胞介素10可抑制肿瘤生长并阻止巨噬细胞浸润。

Interleukin 10 transfected into Chinese hamster ovary cells prevents tumor growth and macrophage infiltration.

作者信息

Richter G, Krüger-Krasagakes S, Hein G, Hüls C, Schmitt E, Diamantstein T, Blankenstein T

机构信息

Institute of Immunology, Klinikum Steglitz, Free University of Berlin, Germany.

出版信息

Cancer Res. 1993 Sep 15;53(18):4134-7.

PMID:8364905
Abstract

Expression of cytokines in tumor cells provides a sensitive modality to analyze the consequences of local cytokines in vivo on tumor infiltrating cells and tumorigenicity. We have transfected Chinese hamster ovary (CHO) cells with an interleukin 10 (IL-10) expression vector. CHO-IL10 cells although unaltered with respect to their in vitro growth lost tumorigenicity, both in nude and in SCID mice and in an IL-10 dose dependent manner. In addition, CHO-IL10 cells suppressed the growth of equal numbers of coinjected but not of contralaterally injected CHO cells. Immunohistology with anti-CR3/Mac-1 and anti-Mac-3 monoclonal antibodies revealed that CHO tumors were substantially infiltrated by macrophages. However, in CHO-IL10 tumors macrophages were virtually absent within the tumor tissue. Our results suggest that IL-10 indirectly suppresses tumor growth of certain tumors by inhibiting infiltration of macrophages which may provide tumor growth promoting activity.

摘要

肿瘤细胞中细胞因子的表达为分析体内局部细胞因子对肿瘤浸润细胞和肿瘤发生的影响提供了一种敏感的方法。我们用白细胞介素10(IL-10)表达载体转染了中国仓鼠卵巢(CHO)细胞。CHO-IL10细胞尽管在体外生长方面未发生改变,但在裸鼠和SCID小鼠中均丧失了致瘤性,且呈IL-10剂量依赖性。此外,CHO-IL10细胞抑制了等量共注射但非对侧注射的CHO细胞的生长。用抗CR3/Mac-1和抗Mac-3单克隆抗体进行免疫组织学分析显示,CHO肿瘤中有大量巨噬细胞浸润。然而,在CHO-IL10肿瘤中,肿瘤组织内几乎没有巨噬细胞。我们的结果表明,IL-10通过抑制可能提供肿瘤生长促进活性的巨噬细胞浸润来间接抑制某些肿瘤的生长。

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