Koba S, Pakala R, Katagiri T, Benedict C R
Department of Internal Medicine, Division of Cardiology, University of Texas Health Science Center at Houston, 6431 Fannin, MSB 6.039, Houston, TX 77030, USA.
Atherosclerosis. 2000 Mar;149(1):61-7. doi: 10.1016/s0021-9150(99)00298-1.
Previous studies have shown that very low density lipoprotein (VLDL), intermediate density lipoprotein (IDL) and low density lipoprotein (LDL) from hyperlipidemic plasma are more atherogenic than those from normal plasma. Since platelet aggregation at sites of atherosclerotic injury exposes the cells to high concentrations of serotonin (5HT), a known mitogen for vascular smooth muscle cells (VSMCs), it was examined whether VLDL, IDL or LDL from plasma of 1% cholesterol-fed rabbits can potentiate the mitogenic effect of 5HT on VSMC.
Growth arrested primary aortic VSMC in 1st or 2nd passage were incubated with different concentrations of VLDL, IDL or LDL in the presence or absence of pertusis toxin (PTX) for 24 h followed by incubation with 5HT for 24 h. The amount of [3H]thymidine incorporated into the DNA as well as the increase in cell number was measured.
Either VLDL, IDL or LDL at a concentration of 60 microg/ml induced proliferation of VSMC by themselves (196, 137 or 122% increase in [3H]thymidine incorporation, or 122, 119 or 122% increase in cell number, respectively when compared to the control, P<0.05). This effect on DNA synthesis was markedly potentiated by 50 microM 5HT to 465, 714 and 1369%, respectively. PTX reversed the mitogenic effect of 5HT, but not that of VLDL, IDL or LDL.
These results suggest that even low concentration of VLDL, IDL or LDL from hypercholesterolemic plasma may significantly potentiate the mitogenic effect of 5HT, that is released by aggregating platelets at sites of vascular damage.
先前的研究表明,高脂血症血浆中的极低密度脂蛋白(VLDL)、中间密度脂蛋白(IDL)和低密度脂蛋白(LDL)比正常血浆中的更具致动脉粥样硬化性。由于动脉粥样硬化损伤部位的血小板聚集使细胞暴露于高浓度的血清素(5HT),而5HT是血管平滑肌细胞(VSMC)已知的促有丝分裂原,因此研究了1%胆固醇喂养兔血浆中的VLDL、IDL或LDL是否能增强5HT对VSMC的促有丝分裂作用。
将第1代或第2代生长停滞的原代主动脉VSMC在有或无百日咳毒素(PTX)的情况下,与不同浓度的VLDL、IDL或LDL孵育24小时,然后与5HT孵育24小时。测量掺入DNA中的[3H]胸腺嘧啶核苷的量以及细胞数量的增加。
浓度为60微克/毫升的VLDL、IDL或LDL自身均可诱导VSMC增殖(与对照组相比,[3H]胸腺嘧啶核苷掺入量分别增加196%、137%或122%,细胞数量分别增加122%、119%或122%,P<0.05)。50微摩尔5HT可将这种对DNA合成的作用显著增强至分别为465%、714%和1369%。PTX可逆转5HT的促有丝分裂作用,但不能逆转VLDL、IDL或LDL的促有丝分裂作用。
这些结果表明,即使是高胆固醇血症血浆中低浓度的VLDL、IDL或LDL也可能显著增强5HT的促有丝分裂作用,5HT是由血管损伤部位聚集的血小板释放的。