Koo E W, Gotlieb A I
Department of Pathology, Banting and Best Diabetes Centre, University of Toronto, Toronto Hospital, Ontario, Canada.
Lab Invest. 1991 Jun;64(6):743-53.
Since intimal smooth muscle cells (SMC) are an important feature of atherosclerotic fibrofatty plaques, we tested the hypothesis that endothelial cells (EC) regulate SMC proliferation in the process of neointimal formation. Using a porcine thoracic aortic organ culture (OC) system, we previously showed in a preliminary study that short-term porcine aortic explants incubated in 5% fetal bovine serum for 7 days promote neointimal formation only in the presence of endothelium or in conditioned media collected from proliferating OC with endothelium present. We now report that these organ cultures can be maintained in culture for up to 4 weeks. The surface cells stained positively for dil-acetylated-low-density lipoprotein throughout the 4-week period indicating the continued presence of EC while the neointimal cells stained positively for the smooth muscle actin-specific monoclonal antibodies alpha-SM1 and HHF-35 indicating their smooth muscle nature. The number of EC did not change during the 4-week incubation period, however, EC turnover peaked at 5 days and remained elevated but constant throughout. The number of intimal SMC doubled between day 0 (18.4 +/- 0.2 cells/field) and day 7 (41.5 +/- 0.9) and between day 7 and day 14 (75.8 +/- 10.1). The intimal SMC number then stabilized thereafter (day 21: 79.5 +/- 7.8, day 28: 73.8 +/- 12.1). Cell proliferation played a large part since autoradiography studies using nondenuded OC showed that intimal SMC thymidine index on day 0 was 1.4% +/- 0.4, peaked at the end of day 5 (25.7% +/- 4.1) and gradually decreased thereafter. The peak in the intimal SMC thymidine index occurred during a period of high EC turnover (maximum EC thymidine index on day 5: 21.8% +/- 2.1), and the stabilization of intimal SMC number observed beyond 2 weeks of incubation occurred when EC replication was reduced (day 14: 6.7% +/- 0.21). Incubation of organ cultures denuded of their endothelium in 5% fetal bovine serum showed a marked decrease in neointimal formation. However, denuded OC when incubated in conditioned medium collected from 4-day-old nondenuded OC (4DCM) enhanced neointimal formation of denuded OC. In contrast, the neointima of denuded OC incubated in 24-day-old nondenuded OC conditioned medium was similar to that of controls. The thymidine index of intimal SMC of denuded OC treated with 4DCM was markedly higher than that found with the control treatment at all time points.(ABSTRACT TRUNCATED AT 400 WORDS)
由于内膜平滑肌细胞(SMC)是动脉粥样硬化纤维脂肪斑块的一个重要特征,我们验证了如下假说:在内膜形成过程中,内皮细胞(EC)调节SMC增殖。利用猪胸主动脉器官培养(OC)系统,我们在之前的一项初步研究中表明,在5%胎牛血清中孵育7天的短期猪主动脉外植体,仅在内皮存在时或存在内皮的增殖性OC收集的条件培养基中,才会促进内膜形成。我们现在报告,这些器官培养物可在培养中维持长达4周。在整个4周期间,表面细胞对dil-乙酰化低密度脂蛋白染色呈阳性,表明EC持续存在,而内膜细胞对平滑肌肌动蛋白特异性单克隆抗体α-SM1和HHF-35染色呈阳性,表明其平滑肌性质。在4周的孵育期内,EC数量没有变化,然而,EC更新在第5天达到峰值,并在整个过程中保持升高但恒定。内膜SMC数量在第0天(每视野18.4±0.2个细胞)和第7天(41.5±0.9)之间以及第7天和第14天(75.8±10.1)之间翻倍。此后内膜SMC数量稳定下来(第21天:79.5±7.8,第28天:73.8±12.1)。细胞增殖起了很大作用,因为使用未剥脱OC的放射自显影研究表明,第0天内膜SMC的胸苷指数为1.4%±0.4,在第5天结束时达到峰值(25.7%±4.1),此后逐渐下降。内膜SMC胸苷指数的峰值出现在EC高更新期(第5天EC胸苷指数最高:21.8%±2.1),并且在孵育2周后观察到的内膜SMC数量稳定发生在EC复制减少时(第14天:6.7%±0.21)。在5%胎牛血清中孵育去除内皮的器官培养物,内膜形成明显减少。然而,去除内皮的OC在从4天龄未剥脱OC收集的条件培养基(4DCM)中孵育时,增强了去除内皮的OC的内膜形成。相比之下,在24天龄未剥脱OC条件培养基中孵育的去除内皮的OC的内膜与对照相似。在所有时间点,用4DCM处理的去除内皮的OC的内膜SMC胸苷指数明显高于对照处理。(摘要截短于400字)