Iwamoto Y, Sugioka Y
Department of Orthopaedic Surgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Adv Exp Med Biol. 1992;324:141-9. doi: 10.1007/978-1-4615-3398-6_14.
We have used an extract of basement membranes which can be reconstituted into a biologically active gel matrix composed predominantly of collagen IV, laminin, nidogen, and heparin sulfate proteoglycan, in order to study the mechanisms involved in tumor cell invasion. When layered onto a porous filter in a Boyden chamber, the gel forms a barrier to the passage of normal cells. Malignant cells are able to cross this layer when the conditioned medium of NIH 3T3 cells is used as a chemoattractant to stimulate cell migration. A variety of human tumor cells have thus been studied in this system and we find a high correlation between their invasiveness in vitro and their malignant behavior as exhibited in vivo. We have used this in vitro invasion assay to test for factors which might inhibit tumor cell invasion. Collagenase IV is produced by malignant cells and is thought to be required for invasion. Indeed, inhibitors of this enzyme have demonstrated reduced tumor cell invasiveness. One site of five amino acids, on the B1 chain, which has been shown to promote cell adhesion, migration and binding to laminin receptor, was found to inhibit the invasion of tumor cells. In addition, factors which elevated cAMP levels were also able to suppress the invasiveness of tumor cells. These data suggest that the assay system described herein can be successfully utilized to study the invasive activity of tumor cells and those factors that may inhibit the spread of malignant cells.
我们使用了一种基底膜提取物,它可以被重构成一种主要由IV型胶原蛋白、层粘连蛋白、巢蛋白和硫酸乙酰肝素蛋白聚糖组成的生物活性凝胶基质,以研究肿瘤细胞侵袭所涉及的机制。当将该凝胶铺在博伊登小室的多孔滤膜上时,它会形成一道阻止正常细胞通过的屏障。当使用NIH 3T3细胞的条件培养基作为趋化剂来刺激细胞迁移时,恶性细胞能够穿过这一层。因此,在这个系统中对多种人类肿瘤细胞进行了研究,我们发现它们在体外的侵袭性与其在体内表现出的恶性行为之间存在高度相关性。我们利用这种体外侵袭试验来检测可能抑制肿瘤细胞侵袭的因素。IV型胶原酶由恶性细胞产生,被认为是侵袭所必需的。事实上,这种酶的抑制剂已证明可降低肿瘤细胞的侵袭性。在B1链上有一个由五个氨基酸组成的位点,已被证明可促进细胞黏附、迁移以及与层粘连蛋白受体的结合,发现该位点能抑制肿瘤细胞的侵袭。此外,提高cAMP水平的因素也能够抑制肿瘤细胞的侵袭性。这些数据表明,本文所述的试验系统可成功用于研究肿瘤细胞的侵袭活性以及那些可能抑制恶性细胞扩散的因素。