Bendeck M P, Irvin C, Reidy M A
Department of Pathology, University of Washington, Seattle, USA.
Circ Res. 1996 Jan;78(1):38-43. doi: 10.1161/01.res.78.1.38.
Smooth muscle cell (SMC) migration and replication are important for neointimal formation after arterial injury. Migration of SMCs requires degradation of basement membrane and extracellular matrix surrounding the cell, and our previous work has shown a correlation between expression of two matrix-degrading metalloproteinases (MMPs), MMP-2 and MMP-9, and smooth muscle migration into the intima in the balloon catheter-injured rat carotid artery. In the present study, an MMP inhibitor, GM 6001, was administered to rats for various times after balloon injury of the carotid artery. Inhibition of MMP activity resulted in a 97% decrease in the number of SMCs that migrated into the intima by 4 days after injury, and lesions growth was retarded by continuous treatment with GM 6001-treated rats was 0.035 +/- 0.008 mm2 compared with 0.095 +/- mm2 in the control group. Neither intimal nor medical SMC replication rates were decreased by GM 6001 treatment, supporting our hypothesis that the decrease in lesion size was due to inhibition of MMP-mediated migration and not inhibition of replication. By 14 days after injury, however, intimal area and SMC number were the same control and inhibitor-treated rats. An increased rate of SMC replication in the GM 6001 rats (replication rates at 10 days were 56.7 +/- 10.0% in the GM 6001 group and 16.97 +/- 1.73% in the control group) contributed to "catch-up" growth of the neointima. Thus, it appears that inhibiting SMC migration with MMP inhibitors is not sufficient to inhibit lesion growth, and lesion size eventually catches up to control via increased SMC replication.
平滑肌细胞(SMC)的迁移和增殖对于动脉损伤后的新生内膜形成至关重要。SMC的迁移需要降解细胞周围的基底膜和细胞外基质,我们之前的研究表明,两种基质降解金属蛋白酶(MMPs),即MMP-2和MMP-9的表达与平滑肌细胞向球囊导管损伤的大鼠颈动脉内膜的迁移之间存在相关性。在本研究中,在大鼠颈动脉球囊损伤后的不同时间给予MMP抑制剂GM 6001。抑制MMP活性导致损伤后4天迁移到内膜的SMC数量减少97%,并且连续用GM 6001治疗可延缓病变生长,GM 6001治疗组大鼠的病变面积为0.035±0.008mm²,而对照组为0.095±mm²。GM 6001治疗并未降低内膜或中膜SMC的增殖率,这支持了我们的假设,即病变大小的减小是由于抑制了MMP介导的迁移而不是抑制增殖。然而,损伤后14天,对照组和抑制剂治疗组的内膜面积和SMC数量相同。GM 6001组大鼠中SMC增殖率增加(GM 6001组10天时的增殖率为56.7±10.0%,对照组为16.97±1.73%)促成了新生内膜的“追赶”生长。因此,似乎用MMP抑制剂抑制SMC迁移不足以抑制病变生长,并且病变大小最终通过增加SMC增殖赶上对照组。