Hailstones D, Sleer L S, Parton R G, Stanley K K
The Heart Research Institute, Camperdown NSW, Sydney, Australia.
J Lipid Res. 1998 Feb;39(2):369-79.
We have examined the expression of caveolin in MDCK cells under conditions that vary cellular cholesterol concentration. Caveolin mRNA levels dropped to one-sixth of control levels after treatment with simvastatin, an inhibitor of cholesterol synthesis, or beta-trimethyl cyclodextrin (CD), a cholesterol sequestering drug. Both simvastatin and CD treatment decreased total cellular cholesterol levels to about 50% of control values. The potent activator of the sterol regulatory element, 25-hydroxycholesterol, showed no direct regulation of caveolin mRNA levels. Caveolin protein concentration was also decreased to 50% of control values in cholesterol-depleted cells, giving rise to a severe attenuation of caveolin expression detected by indirect immunofluorescence labeling. Quantitative electron microscopy showed a total loss of morphologically recognizable invaginated caveolae after these cholesterol depletion treatments. When the number of invaginated caveolae per cell was expressed as a function of the cellular cholesterol content, a threshold phenomenon was observed, suggesting that caveolae only form when the steady state cellular cholesterol is above 50% of control values. These findings indicate that caveolins, and caveolae, may play an important part in cellular cholesterol homeostasis.
我们检测了在细胞胆固醇浓度不同的条件下,MDCK细胞中小窝蛋白的表达情况。在用胆固醇合成抑制剂辛伐他汀或胆固醇螯合剂β-环糊精(CD)处理后,小窝蛋白mRNA水平降至对照水平的六分之一。辛伐他汀和CD处理均使细胞总胆固醇水平降至对照值的约50%。固醇调节元件的强效激活剂25-羟基胆固醇对小窝蛋白mRNA水平无直接调节作用。在胆固醇耗竭的细胞中,小窝蛋白的蛋白浓度也降至对照值的50%,通过间接免疫荧光标记检测到小窝蛋白表达严重减弱。定量电子显微镜显示,这些胆固醇耗竭处理后,形态上可识别的内陷小窝完全消失。当将每个细胞内陷小窝的数量表示为细胞胆固醇含量的函数时,观察到一种阈值现象,表明只有当细胞内稳态胆固醇高于对照值的50%时,小窝才会形成。这些发现表明,小窝蛋白和小窝可能在细胞胆固醇稳态中发挥重要作用。