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刺激牛肾上腺嗜铬细胞中的颗粒肿胀:受颗粒内部pH值调节

Granule swelling in stimulated bovine adrenal chromaffin cells: regulation by internal granule pH.

作者信息

Ornberg R L, Furuya S, Goping G, Kuijpers G A

机构信息

Laboratory of Cell Biology and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.

出版信息

Cell Tissue Res. 1995 Jan;279(1):85-92. doi: 10.1007/BF00300694.

Abstract

Adrenal medullary chromaffin cells secrete catecholamines through exocytosis of their intracellular chromaffin granules. Osmotic granule swelling has been implicated to play a role in the generation of membrane stress associated with the fusion of the granule membrane. However, controversy exists as to whether swelling occurs before or after the actual fusion event. Using morphometric methods we have determined the granule diameter distributions in rapidly frozen, freeze-substituted chromaffin cells. Our measurements show that intracellular chromaffin granules increase in size from an average of 234 nm to 274 nm or 277 nm in cells stimulated to secrete with nicotine or high external K+, respectively. Granule swelling occurs before the formation of membrane contact. Ammonium chloride, an agent which inhibits stimulated catecholamine secretion by approximately 50% by altering the intragranular pH, also inhibits granule swelling. In addition, ammonium chloride-treated secreting cells show more granule-plasma membrane contacts than untreated secreting cells. Sodium propionate induces granule swelling in the absence of secretagogue and has been shown to enhance nicotine- and high K(+)- induced catecholamine release. These results indicate that in adrenal chromaffin cells granule swelling is an essential step in exocytosis before fusion pore formation, and is related to the pH of the granule environment.

摘要

肾上腺髓质嗜铬细胞通过其细胞内嗜铬颗粒的胞吐作用分泌儿茶酚胺。渗透压导致的颗粒肿胀被认为在与颗粒膜融合相关的膜应激产生中起作用。然而,关于肿胀是在实际融合事件之前还是之后发生存在争议。我们使用形态测量方法确定了快速冷冻、冷冻替代的嗜铬细胞中颗粒直径分布。我们的测量结果表明,在用尼古丁或高细胞外钾离子刺激分泌的细胞中,细胞内嗜铬颗粒的大小分别从平均234纳米增加到274纳米或277纳米。颗粒肿胀发生在膜接触形成之前。氯化铵通过改变颗粒内pH值抑制约50%的刺激儿茶酚胺分泌,也抑制颗粒肿胀。此外,经氯化铵处理的分泌细胞比未处理的分泌细胞显示出更多的颗粒-质膜接触。丙酸钠在没有促分泌剂的情况下诱导颗粒肿胀,并已被证明能增强尼古丁和高钾诱导的儿茶酚胺释放。这些结果表明,在肾上腺嗜铬细胞中,颗粒肿胀是融合孔形成之前胞吐作用的一个必要步骤,并且与颗粒环境的pH值有关。

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