Chou Y Y, Lee Y S
Cardiovascular Department, Electron Microscopy Center, Chang Gung Memorial Hospital, Chang Gung College of Medicine and Technology, Taipei, Taiwan, China.
Chin Med J (Engl). 1998 Nov;111(11):1018-24.
To characterize ultrastructurally and biochemically catecholamine release mechanisms of cultured human pheochromocytoma cells in the basal and stimulated states.
The cultured pheochromocytoma cells were prepared from human adrenal pheochromocytoma tumors. Biochemical determinations of catecholamine secretion from the cultured cells were carried out in the basal and stimulated states. Transmission electron microscopy was used to observe the modes of catecholamine release from the cells without and with stimulation by depolarization of the cells with the administration of 50 mmol/L KCl.
Biochemical determinations consistently showed spontaneous secretion of catecholamines from the cultured cells in the basal state without stimulation. Catecholamine release in a calcium-dependent manner could be enhanced in the cells in response to high extracellular potassium concentration. A series of electron microscopic observations of the cultured cells consistently disclosed the classical exocytotic profiles on the cell surface in the basal state. In addition to abundant increase in the number of classical single exocytosis, compound exocytosis was frequently observed in the stimulated cells. Furthermore, other modes of catecholamine release mechanism involving the formation of pseudopodial and/or tubule-like structures, which were different from classical exocytosis, were often present in the intensely stimulation cells.
Based on the biochemical and electron microscopic findings, we concluded: (1) classical single exocytosis is considered to be a primary mechanism responsible for spontaneous secretion of catecholamines from the cells in the basal state; (2) compound exocytosis is an essential mechanism for extruding large amounts of catecholamines in the stimulated cells; and (3) other modes of catecholamine release mechanism may operate in the cells in response to intense stimulation. These morphological data may be helpful in explanation of biochemical variability and extreme diversity of clinical manifestations in patients with pheochromocytoma tumor.
从超微结构和生化方面对培养的人嗜铬细胞瘤细胞在基础状态和刺激状态下的儿茶酚胺释放机制进行表征。
培养的嗜铬细胞瘤细胞取自人肾上腺嗜铬细胞瘤肿瘤。对培养细胞在基础状态和刺激状态下的儿茶酚胺分泌进行生化测定。使用透射电子显微镜观察细胞在未受刺激以及通过给予50 mmol/L氯化钾使细胞去极化而受到刺激时儿茶酚胺的释放方式。
生化测定始终显示,在基础状态下未受刺激时,培养细胞会自发分泌儿茶酚胺。细胞对高细胞外钾浓度的反应中,儿茶酚胺以钙依赖方式释放可增强。对培养细胞的一系列电子显微镜观察始终揭示了基础状态下细胞表面的经典胞吐模式。除了经典的单个胞吐数量大量增加外,在受刺激的细胞中还经常观察到复合胞吐。此外,在强烈刺激的细胞中,经常存在涉及伪足和/或管状结构形成的其他儿茶酚胺释放机制模式,这与经典胞吐不同。
基于生化和电子显微镜研究结果,我们得出以下结论:(1)经典的单个胞吐被认为是基础状态下细胞自发分泌儿茶酚胺的主要机制;(2)复合胞吐是受刺激细胞中挤出大量儿茶酚胺的重要机制;(3)其他儿茶酚胺释放机制模式可能在细胞对强烈刺激的反应中起作用。这些形态学数据可能有助于解释嗜铬细胞瘤患者生化变异性和临床表现的极端多样性。