Thomopoulos G N, Garrett J R, Proctor G B, Hartley R, Zhang X S
Aristotle University of Thessaloniki, School of Sciences, Department of Biology, Greece.
Microsc Res Tech. 1996 Dec 1;35(5):365-76. doi: 10.1002/(SICI)1097-0029(19961201)35:5<365::AID-JEMT1>3.0.CO;2-K.
Sequential secretory changes in granular tubule cells caused by the secretagogue cyclocytidine (75 mg/kg i.p.) were studied at the ultrastructural level, in perfusion (n = 5 animals) and immersion (n = 8 animals) fixed rat submandibular glands, using the periodic acid-thiocarbohydrazide-silver proteinate technique (PA-TCH-SP). The onset of secretion varied from 45 to 75 minutes after administering the cyclocytidine. During the initial stages of overt secretion, structural changes occurred irregularly in a progressive fashion with: (1) an increase in granule membrane staining with PA-TCH-SP and a parallel alignment of the secretory granules with the adjacent apical plasma membrane, which developed a honeycomb-like appearance; (2) docking of these secretory granules to the apical plasma membrane; (3) early secretion of some secretory granules in a semiclassical exocytotic fashion (but this was rarely witnessed). During stages (1) and (2), the cytochemical characteristics of the membrane of the secretory granules, as well as of the plasma membrane, suggest a priming process is occurring. After these initial preparatory phases, further structural changes occurred in the granule membranes with a gradually progressive formation of microvesicles and granule fusions; secretion continued in an explosive manner with proteinaceous material being transferred to lumina in at least three different ways: (1) by typical exocytosis (but it was infrequent); (2) from granules fused intracellularly into aggregates (compound exocytosis); and (3) some apocrine-type of secretion through bleb formation. The formation of these intracellular aggregations was associated with the microvesicles in the granule membranes and some aggregates became very large. Secretion of their contents into lumina occurred through elongated membrane channels. The material secreted included microvesicular forms that had become interiorised in the granular aggregates, and any cytoplasm that may also have been entrapped.
采用高碘酸 - 硫代碳酰肼 - 银蛋白技术(PA - TCH - SP),在超微结构水平上研究了促分泌剂环胞苷(腹腔注射75mg/kg)引起的大鼠颌下腺颗粒小管细胞的顺序性分泌变化,实验采用灌注固定(n = 5只动物)和浸入固定(n = 8只动物)的大鼠颌下腺。环胞苷给药后45至75分钟开始分泌。在明显分泌的初始阶段,结构变化以渐进方式不规则发生,表现为:(1)PA - TCH - SP对颗粒膜的染色增加,分泌颗粒与相邻顶端质膜平行排列,顶端质膜呈现蜂窝状外观;(2)这些分泌颗粒与顶端质膜对接;(3)一些分泌颗粒以半经典的胞吐方式早期分泌(但很少见到)。在(1)和(2)阶段,分泌颗粒膜以及质膜的细胞化学特征表明正在发生引发过程。在这些初始准备阶段之后,颗粒膜发生进一步的结构变化,微泡逐渐形成且颗粒融合;分泌以爆发方式持续,蛋白质物质至少通过三种不同方式转移到管腔中:(1)通过典型的胞吐作用(但不常见);(2)颗粒在细胞内融合形成聚集体(复合胞吐作用);(3)通过形成泡状突起进行一些顶浆分泌型分泌。这些细胞内聚集体的形成与颗粒膜中的微泡有关,一些聚集体变得非常大。它们的内容物通过细长的膜通道分泌到管腔中。分泌的物质包括已内化到颗粒聚集体中的微泡形式,以及可能也被截留的任何细胞质。