Kawashima A, Nakanishi I, Tsuchiya H, Roessner A, Obata K, Okada Y
Department of Pathology, School of Medicine, Kanazawa University, Ishikawa, Japan.
Virchows Arch. 1994;424(5):547-52. doi: 10.1007/BF00191442.
We have examined the correlation between matrix metalloproteinase (MMP) expression and metastatic properties of a low metastatic osteosarcoma cell line, osteosarcoma takase (OST), under stimulation by tumour necrosis factor alpha (TNF alpha). In vivo, OST cells exhibited significantly increased colonization in the lungs of nude mice in a dose-dependent manner when they were treated by TNF alpha prior to injection. In vitro, TNF alpha enhanced tumour cell invasion through the reconstituted basement membrane in a transwell chamber up to 2.5-fold. Gelatin zymography and sandwich enzyme immunoassays demonstrated marked production of MMP-9 [92-kDa gelatinase/type IV collagenase (gelatinase B)] but not MMP-2 [72-kDa gelatinase/type IV collagenase (gelatinase A)], MMP-3 (stromelysin-1) or MMP-7 (matrilysin). Motility of the tumour cells and adhesion to cultured endothelial cells were slightly increased by the TNF alpha treatment up to 1.6-fold and 1.4-fold, respectively, while the growth rate was decreased. These results suggest that upregulation of MMP-9 together with enhanced motility and endothelial adhesion contribute to the increased metastatic ability of OST cells induced by TNF alpha treatment.
我们研究了在肿瘤坏死因子α(TNFα)刺激下,低转移性骨肉瘤细胞系骨肉瘤高濑(OST)的基质金属蛋白酶(MMP)表达与转移特性之间的相关性。在体内,当在注射前用TNFα处理时,OST细胞在裸鼠肺中的定植以剂量依赖性方式显著增加。在体外,TNFα使肿瘤细胞通过Transwell小室中的重组基底膜的侵袭增强了2.5倍。明胶酶谱法和夹心酶免疫测定法显示MMP-9[92 kDa明胶酶/IV型胶原酶(明胶酶B)]有显著产生,但MMP-2[72 kDa明胶酶/IV型胶原酶(明胶酶A)]、MMP-3(基质溶解素-1)或MMP-7(基质溶素)没有。TNFα处理使肿瘤细胞的运动性和对培养内皮细胞的粘附性分别略有增加,最高可达1.6倍和1.4倍,而生长速率降低。这些结果表明,MMP-9的上调以及运动性和内皮粘附性的增强有助于TNFα处理诱导的OST细胞转移能力的增加。