Pavelka M, Ellinger A
J Cell Biol. 1983 Sep;97(3):737-48. doi: 10.1083/jcb.97.3.737.
Colchicine administered to adult rats at a dosage of 0.5 mg/100 g of body weight effected a disorganization of the Golgi apparatus in pancreatic acinar cells. The results obtained after various periods of treatment (10 min to 6 h) showed (a) changes in all components of the Golgi complex, and (b) occurrence of large vacuoles that predominated in cytoplasmic areas outside the Golgi region. The alterations in Golgi stacks concerned elements of the proximal and distal side: (a) accumulation of transport vesicles, (b) formation of small, polymorphic secretion granules, and (c) alterations in the cytochemical localization of enzymes and reaction product after osmification. Transport vesicles accumulated and accompanied short, dilated cisternae, which lack mostly the reaction products of thiamine pyrophosphatase, inosine diphosphatase, and acid phosphatase, and osmium deposits after prolonged osmification. After 4 to 6 h of treatment, accumulated transport vesicles occupied extensive cellular areas; stacked cisternae were not demonstrable in these regions. The changes on the distal Golgi side included GERL elements: condensing vacuoles were diminished; they were substituted by small, polymorphic zymogen granules, which appeared to be formed by distal Golgi cisternae and by rigid lamellae. Unusually extended coated regions covered condensing vacuoles, rigid lamellae, and polymorphic secretion granules. A cytochemical distinction between Golgi components and GERL was possible neither in controls nor after colchicine treatment. The cytochemical alterations in Golgi components were demonstrable 20-30 min following administration of colchicine; at 45 min, initial morphological changes--augmentation of transport vesicles and formation of polymorphic zymogen granules--became apparent. 20 min after administration of colchicine, conspicuous groups of large vacuoles occurred. They were located mostly in distinct fields between cisternae of the endoplasmic reticulum, and were accompanied by small osmium--reactive vesicles. Stacked cisternae were not demonstrable in these fields. Vacuoles and vesicles were devoid of reaction products of thiamine pyrophosphatase, inosine diphosphatase, and acid phosphatase. The results provide evidence that formation of stacked Golgi cisternae is impaired after colchicine treatment. The colchicine--induced disintegration of the Golgi complex suggests a regulatory function of microtubules in the organization of the Golgi apparatus.
给成年大鼠按0.5毫克/100克体重的剂量注射秋水仙碱,会导致胰腺腺泡细胞中高尔基体的结构紊乱。在不同治疗时间段(10分钟至6小时)后获得的结果显示:(a)高尔基体复合体的所有成分发生变化;(b)出现大液泡,主要集中在高尔基体区域外的细胞质区域。高尔基体堆叠的改变涉及近端和远端的成分:(a)运输小泡的积累;(b)形成小的、多形性的分泌颗粒;(c)在锇化后,酶和反应产物的细胞化学定位发生改变。运输小泡积累并伴随着短而扩张的扁平囊,这些扁平囊大多缺乏硫胺素焦磷酸酶、肌苷二磷酸酶和酸性磷酸酶的反应产物,并且在长时间锇化后缺乏锇沉积。治疗4至6小时后,积累的运输小泡占据了广泛的细胞区域;在这些区域中无法观察到堆叠的扁平囊。高尔基体远端的变化包括GERL成分:浓缩泡减少;它们被小的、多形性的酶原颗粒取代,这些酶原颗粒似乎是由高尔基体远端扁平囊和刚性薄片形成的。异常延伸的被膜区域覆盖着浓缩泡、刚性薄片和多形性分泌颗粒。在对照组和秋水仙碱治疗后,都无法在细胞化学上区分高尔基体成分和GERL。在注射秋水仙碱后20 - 30分钟,高尔基体成分的细胞化学改变就可以显现出来;在45分钟时,最初的形态学变化——运输小泡增加和多形性酶原颗粒形成——变得明显。注射秋水仙碱20分钟后,出现明显的大液泡群。它们大多位于内质网扁平囊之间的不同区域,并伴有小的锇反应性小泡。在这些区域中无法观察到堆叠的扁平囊。液泡和小泡缺乏硫胺素焦磷酸酶、肌苷二磷酸酶和酸性磷酸酶的反应产物。这些结果证明,秋水仙碱治疗后高尔基体堆叠扁平囊的形成受到损害。秋水仙碱诱导的高尔基体复合体解体表明微管在高尔基体的组织中具有调节功能。