Kubota S, Takeda K, Yamada T, Nomura Y, Takeda M, Iwamoto S, Seyama Y
Department of Physiological Chemistry and Nutrition, Faculty of Medicine, University of Tokyo, Japan.
Cancer Lett. 1996 Jan 2;98(2):233-40.
We have examined the effects of tumor necrosis factor alpha (TNF) and lymphotoxin (LT) on gelatinase (72 kDa and 92 kDa) and tissue inhibitor of metalloprotease 1 (TIMP1) secretion by human myeloblastic leukemia cells (ML-1) in vitro. TNF (0.1-30 ng/ml) significantly stimulated 92 kDa gelatinase secretion in a dose-dependent manner, but did not significantly stimulate 72 kDa gelatinase secretion. LT also significantly stimulated 92 kDa gelatinase secretion, but the stimulation was less effective compared to TNF. TNF, but not LT, concentrations at 30 ng/ml slightly stimulated TIMP1 secretion. Because 92 kDa gelatinase is thought to play a pivotal role in tumor invasion, we examined the effect of TNF or LT on ML-1 cell invasion through a reconstituted basement membrane (Matrigel). Exposure of ML-1 cells to TNF (3, 10, and 30 ng/ml) or LT (3, 10, and 30 ng/ml) stimulated ML-1 cell invasion through Matrigel in a dose-dependent manner in vitro. The data suggest that TNF- and LT-stimulated 92 kDa gelatinase secretion could play an important role in TNF- or LT-stimulated ML-1 cell invasion.
我们已经在体外研究了肿瘤坏死因子α(TNF)和淋巴毒素(LT)对人成髓细胞白血病细胞(ML-1)分泌明胶酶(72 kDa和92 kDa)及金属蛋白酶组织抑制剂1(TIMP1)的影响。TNF(0.1 - 30 ng/ml)以剂量依赖的方式显著刺激92 kDa明胶酶的分泌,但对72 kDa明胶酶的分泌没有显著刺激作用。LT也显著刺激92 kDa明胶酶的分泌,但与TNF相比,这种刺激作用较弱。30 ng/ml的TNF浓度轻微刺激TIMP1的分泌,而LT则无此作用。由于92 kDa明胶酶被认为在肿瘤侵袭中起关键作用,我们研究了TNF或LT对ML-1细胞通过重组基底膜(基质胶)侵袭的影响。体外实验中,将ML-1细胞暴露于TNF(3、10和30 ng/ml)或LT(3、10和30 ng/ml)以剂量依赖的方式刺激ML-1细胞通过基质胶侵袭。数据表明,TNF和LT刺激的92 kDa明胶酶分泌可能在TNF或LT刺激的ML-1细胞侵袭中起重要作用。