Andreis P G, Rebuffat P, Belloni A S, Neri G, Cavallini L, Gottardo G, Mazzocchi G, Coi A, Malendowicz L K, Nussdorfer G G
Department of Anatomy, University of Padua, Italy.
Cell Tissue Res. 1989 Oct;258(1):43-51. doi: 10.1007/BF00223143.
The morphology and function of isolated inner (zona fasciculata/reticularis) adrenocortical cells of rats pretreated with ACTH for 3, 6, 9 or 12 days were investigated. ACTH treatment induced a notable time-dependent enhancement in the steroidogenic capacity (corticosterone production) and growth of inner cells. The volumes of cells, mitochondrial compartment, membrane space [the cellular space occupied by smooth endoplasmic reticulum (SER) membranes] and lipid-droplet compartment, as well as the surface area of mitochondrial cristae and SER tubules, were increased in relation to the duration of ACTH pretreatment, and showed a highly significant positive linear correlation with both basal and stimulated corticosterone production. The acute exposure of isolated cells to ACTH provoked a striking lipid-droplet depletion, the extent of which was linearly and positively correlated with stimulated corticosterone secretion. The hypertrophy of the mitochondrial compartment and SER are interpreted as the morphological counterpart of the enhanced steroidogenic capacity of inner adrenocortical cells, inasmuch as the enzymes of steroid synthesis are located in these two organelles, and it is well known that chronic ACTH exposure stimulates the de novo synthesis of many of them in vivo. The rise in the number of lipid droplets, in which cholesterol is stored, is interpreted as being due to the fact that, under chronic ACTH treatment, the processes leading to cholesterol accumulation in adrenocortical cells (exogenous uptake and endogenous synthesis) exceed those of its utilization in basal steroid secretion. Cholesterol accumulated in lipid droplets as a reserve material may be rapidly utilized after acute ACTH exposure to meet the needs of the enhanced steroidogenic capacity of adrenocortical cells.
对用促肾上腺皮质激素(ACTH)预处理3、6、9或12天的大鼠分离的肾上腺皮质内层(束状带/网状带)细胞的形态和功能进行了研究。ACTH处理导致内层细胞的类固醇生成能力(皮质酮产生)和生长出现显著的时间依赖性增强。细胞、线粒体区室、膜空间[由滑面内质网(SER)膜占据的细胞空间]和脂滴区室的体积,以及线粒体嵴和SER小管的表面积,均随着ACTH预处理时间的延长而增加,并且与基础和刺激状态下的皮质酮产生均呈现高度显著的正线性相关。分离的细胞急性暴露于ACTH会引发显著的脂滴消耗,其程度与刺激后的皮质酮分泌呈线性正相关。线粒体区室和SER的肥大被解释为肾上腺皮质内层细胞类固醇生成能力增强的形态学对应物,因为类固醇合成酶位于这两个细胞器中,并且众所周知,长期暴露于ACTH会在体内刺激其中许多酶的从头合成。储存胆固醇的脂滴数量增加被解释为是由于在长期ACTH治疗下,肾上腺皮质细胞中导致胆固醇积累的过程(外源性摄取和内源性合成)超过了其在基础类固醇分泌中的利用过程。急性暴露于ACTH后,脂滴中积累的作为储备物质的胆固醇可被迅速利用,以满足肾上腺皮质细胞增强的类固醇生成能力的需求。