Page E, Upshaw-Earley J, Goings G E
Department of Medicine, University of Chicago, Ill 60637.
Circ Res. 1994 Nov;75(5):949-54. doi: 10.1161/01.res.75.5.949.
The plasma membrane-associated non-clathrin-coated vesicles called caveolae are multifunctional organelles thought to be implicated in the sequestration and transport of small molecules (potocytosis) as well as in the binding of Ca2+ ions, signal transduction, and processing of hormonal and mechanosensitive signals. We have previously suggested that the apparent contiguity of caveolar and atrial granule membranes observed in electron micrographs of in situ mouse atrial myocytes might reflect externalization of atrial natriuretic peptide through caveolae. Using Tokuyasu's classic technique, we now show by immunoelectron microscopy of glutaraldehyde-fixed and cryosectioned mouse and rat atria that antibody against atrial natriuretic peptide prohormone is present within caveolae of in situ atrial myocytes. We confirm this intracaveolar localization by stereoimaging colloidal gold-labeled antibody to the prohormone in electron micrographs of glutaraldehyde/osmium tetroxide-fixed positively stained atrial thin sections. Because profiles of caveolae were rarely immunolabeled with antibody against atrial peptide unless there was a profile of an immunolabeled atrial granule nearby in the subjacent cytoplasm, we concluded that the intracaveolar hormone was derived predominantly from a direct interaction of atrial granules with caveolae. Perturbations that markedly increase the rate of natriuretic peptide secretion via the regulated pathway, including atrial stretch, contractions, and increased external Ca2+ concentration, failed to alter caveolar immunostaining. These results suggest that atrial peptide can pass from atrial granules into caveolae by transiently open pathways between the interiors of granules and caveolae. The results are interpreted as suggesting the presence of a second pathway for externalization of atrial natriuretic peptide through caveolae in addition to the classic pathway for regulated atrial peptide secretion at noncaveolar plasmalemma.
一种被称为小窝的与质膜相关的非网格蛋白包被小泡是多功能细胞器,被认为与小分子的隔离和运输(胞饮作用)以及钙离子的结合、信号转导、激素和机械敏感信号的处理有关。我们之前曾提出,在原位小鼠心房肌细胞的电子显微照片中观察到的小窝和心房颗粒膜的明显连续性可能反映了心房利钠肽通过小窝的外排。使用德久的经典技术,我们现在通过对戊二醛固定并冷冻切片的小鼠和大鼠心房进行免疫电子显微镜检查发现,抗心房利钠肽原激素的抗体存在于原位心房肌细胞的小窝内。我们通过对戊二醛/四氧化锇固定并阳性染色的心房薄片的电子显微照片中前激素的胶体金标记抗体进行立体成像,证实了这种小窝内定位。因为除非在相邻细胞质中有免疫标记的心房颗粒轮廓,否则小窝轮廓很少被抗心房肽抗体免疫标记,所以我们得出结论,小窝内的激素主要来自心房颗粒与小窝的直接相互作用。通过调节途径显著增加利钠肽分泌速率的扰动,包括心房牵张、收缩和细胞外钙离子浓度增加,均未能改变小窝的免疫染色。这些结果表明,心房肽可以通过颗粒内部和小窝之间短暂开放的途径从心房颗粒进入小窝。这些结果被解释为表明除了在非小窝质膜处调节心房肽分泌的经典途径外,还存在通过小窝使心房利钠肽外排的第二条途径。