Gavrilovic J, Murphy G
Cell Physiology Department, Strangeways Research Laboratory, Cambridge, U.K.
Cell Biol Int Rep. 1989 Apr;13(4):367-75. doi: 10.1016/0309-1651(89)90163-x.
The ability of VX2 tumour cells and chondrocytes to degrade radiolabelled collagen films was shown to be dependent on the presence of the serum proteinase plasminogen. Degradation of collagen films in the presence of plasminogen was inhibited by addition of exogenous TIMP indicating that such lysis was mediated by collagenase. VX2 cells required ten times less plasminogen than chondrocytes to effect comparable degradation; this result was probably related to the observation that VX2 cells did not synthesize the specific tissue inhibitor of metalloproteinases, TIMP.
VX2肿瘤细胞和软骨细胞降解放射性标记胶原膜的能力被证明取决于血清蛋白酶纤溶酶原的存在。在外源性组织金属蛋白酶抑制剂(TIMP)存在的情况下,纤溶酶原存在时胶原膜的降解受到抑制,这表明这种溶解是由胶原酶介导的。VX2细胞所需的纤溶酶原比软骨细胞少十倍就能产生相当程度的降解;这一结果可能与观察到VX2细胞不合成金属蛋白酶特异性组织抑制剂TIMP有关。