Dejana E, Bertocchi F, Bortolami M C, Regonesi A, Tonta A, Breviario F, Giavazzi R
Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
J Clin Invest. 1988 Oct;82(4):1466-70. doi: 10.1172/JCI113753.
We report that IL 1 acts on the endothelium, inducing a long-lasting increase in its adhesivity to tumor cells. Selective pretreatment of cultured human umbilical vein endothelial cells (EC) with IL 1 caused a significant increase in adhesion of three human colorectal carcinoma (HT-29, HCC-P2988, and HCC-M1410) cell lines and one human melanoma (A-375) cell line. Tumor necrosis factor (TNF) was as effective as IL 1 in promoting tumor cell adhesion to EC, whereas IFN gamma and IL 2 were inactive. The IL 1 and TNF induction of EC adhesivity was both concentration (threshold concentration 1 U/ml) and time dependent (peak 4-6 h), reversible within 24 h, and blocked by a protein synthesis inhibitor. The IL 1 and TNF action on EC may play a role in tumor cell lodgement.
我们报告白细胞介素1作用于内皮细胞,可使其对肿瘤细胞的黏附性持久增加。用白细胞介素1对培养的人脐静脉内皮细胞(EC)进行选择性预处理,会导致三种人结肠癌细胞系(HT - 29、HCC - P2988和HCC - M1410)以及一种人黑色素瘤细胞系(A - 375)的黏附显著增加。肿瘤坏死因子(TNF)在促进肿瘤细胞与内皮细胞黏附方面与白细胞介素1同样有效,而干扰素γ和白细胞介素2则无活性。白细胞介素1和肿瘤坏死因子对内皮细胞黏附性的诱导作用均具有浓度依赖性(阈值浓度为1 U/ml)和时间依赖性(峰值在4 - 6小时),在24小时内可逆转,且被蛋白质合成抑制剂阻断。白细胞介素1和肿瘤坏死因子对内皮细胞的作用可能在肿瘤细胞着床过程中发挥作用。