Durand P, Cathiard A M, Naaman E, Brieu V, Saez J M
J Steroid Biochem. 1987 Apr;26(4):425-31. doi: 10.1016/0022-4731(87)90051-3.
The present study examined the effects of serum and lipoproteins on the function of cultured adrenal cells from 115-127-day-old ovine fetuses and from newborn lambs. On day 1 of culture, corticosteroid output was similar in medium containing 2% horse serum or in serum-free medium, both for fetal and neonatal cells. However, on day 5, cells cultured in the absence of serum produced smaller amounts of these steroids than cells maintained in medium containing serum; the difference was more marked under ACTH1-24 stimulation. Conversely, cAMP production was never lower in the absence than in the presence of serum. When stimulated by ACTH1-24 on day 2 of culture, fetal or neonatal adrenal cells incubated in the presence of a saturating concentration of ovine LDL produced more corticosteroids than cells incubated in serum-free medium; HDL also enhanced ACTH1-24-induced steroidogenesis, but to a lesser extent. VLDL was effective only with neonatal cells. In fetal and neonatal cells cultured for 6 days in ACTH-free medium, VLDL and LDL increased ACTH-induced steroidogenesis, but HDL did not. On the other hand, when cells were cultured in the presence of ACTH1-24, LDL and HDL were equipotent in supporting ACTH1-24-induced steroid output. Three major lipoprotein fractions were observed in serum of fetal and newborn lambs. The concentration of cholesterol was very low in the VLDL fraction of fetuses, but it was similar to that of newborns in LDL. Conversely, 4 times more cholesterol was present in HDL of newborns than in HDL of fetuses. These results suggest that: (i) after several days of cell culture, cholesterol availability is an important limiting factor for the steroidogenesis of cells maintained under serum-free conditions; (ii) both an "LDL pathway" and an "HDL pathway" are operating in adrenal cells from fetal as well as newborn sheep; (iii) LDL and HDL are important physiological sources of cholesterol to support steroidogenesis by fetal and neonatal adrenal cells.
本研究检测了血清和脂蛋白对115 - 127日龄绵羊胎儿及新生羔羊培养肾上腺细胞功能的影响。在培养第1天,无论是含2%马血清的培养基还是无血清培养基,胎儿和新生细胞的皮质类固醇产量相似。然而,在第5天,无血清培养的细胞产生的这些类固醇量比含血清培养基中培养的细胞少;在促肾上腺皮质激素1 - 24刺激下,这种差异更为明显。相反,无血清时cAMP的产生从未低于有血清时。在培养第2天用促肾上腺皮质激素1 - 24刺激时,在饱和浓度的绵羊低密度脂蛋白存在下孵育的胎儿或新生肾上腺细胞比在无血清培养基中孵育的细胞产生更多的皮质类固醇;高密度脂蛋白也增强了促肾上腺皮质激素1 - 24诱导的类固醇生成,但程度较小。极低密度脂蛋白仅对新生细胞有效。在无促肾上腺皮质激素培养基中培养6天的胎儿和新生细胞中,极低密度脂蛋白和低密度脂蛋白增加了促肾上腺皮质激素诱导的类固醇生成,但高密度脂蛋白没有。另一方面,当细胞在促肾上腺皮质激素1 - 24存在下培养时,低密度脂蛋白和高密度脂蛋白在支持促肾上腺皮质激素1 - 24诱导的类固醇产量方面效力相当。在胎儿和新生羔羊的血清中观察到三种主要的脂蛋白组分。胎儿极低密度脂蛋白组分中的胆固醇浓度非常低,但与新生羔羊低密度脂蛋白中的胆固醇浓度相似。相反,新生羔羊高密度脂蛋白中的胆固醇含量是胎儿高密度脂蛋白中的4倍。这些结果表明:(i)细胞培养几天后,胆固醇的可利用性是无血清条件下培养细胞类固醇生成的重要限制因素;(ii)“低密度脂蛋白途径”和“高密度脂蛋白途径”在胎儿和新生绵羊的肾上腺细胞中均起作用;(iii)低密度脂蛋白和高密度脂蛋白是胎儿和新生肾上腺细胞支持类固醇生成的重要胆固醇生理来源。