Wick P F, Trenkle J M, Holz R W
Department of Pharmacology, University of Michigan Medical School, Ann Arbor 48109-0632, U.S.A.
Neuroscience. 1997 Oct;80(3):847-60. doi: 10.1016/s0306-4522(97)00062-6.
A secretion from cultured bovine chromaffin cells was stimulated to examine the pattern of exocytotic fusion on the plasma membrane. Confocal microscopy revealed that dopamine-beta-hydroxylase immunofluorescence in intact cells stimulated for 20s with the nicotinic agonist 1,1-dimethyl-4-phenylpiperazinium was almost entirely punctate and evenly distributed on the cell surface. The basis for the fine, punctate appearance of dopamine-beta-hydroxylase was investigated. Dopamine-beta-hydroxylase presentation on the surface of permeabilized cells stimulated with 1-30 microM Ca2+ was punctate and similar to that on the plasma membrane of intact cells. The fluorescence intensities of both surface dopamine-beta-hydroxylase sites and internal chromaffin granules were estimated by computerized digital image analysis. The surface area of punctate surface dopamine-beta-hydroxylase (0.218 +/- 0.013 microm2, mean +/- S.E.M.) is similar to the surface area of a 0.28 microm diameter chromaffin granule (0.25 microm2). The average fluorescence intensity integrated over the area of the surface spots was 25-30% of the average chromaffin granule intensity, a fraction that is similar to the published values of 40-50% of the dopamine-beta-hydroxylase in the chromaffin granule being membrane bound. The surface density of the spots is consistent with the number of granules undergoing exocytosis. The spots do not tend to be clumped. The key conclusions from this work are that each individual punctate site of dopamine-beta-hydroxylase represents the fusion of a single chromaffin granule and that the distribution of dopamine-beta-hydroxylase spots over the cell surface is extensive and random, suggesting that each individual granule associates with its own release site.
为了研究质膜上胞吐融合的模式,对培养的牛嗜铬细胞的分泌物进行了刺激。共聚焦显微镜显示,用烟碱激动剂1,1 - 二甲基 - 4 - 苯基哌嗪刺激完整细胞20秒后,多巴胺β - 羟化酶免疫荧光几乎完全呈点状,且均匀分布在细胞表面。对多巴胺β - 羟化酶精细点状外观的基础进行了研究。用1 - 30 microM Ca2 +刺激的通透细胞表面的多巴胺β - 羟化酶呈现点状,与完整细胞质膜上的相似。通过计算机数字图像分析估算了表面多巴胺β - 羟化酶位点和内部嗜铬颗粒的荧光强度。点状表面多巴胺β - 羟化酶的表面积(0.218±0.013平方微米,平均值±标准误)与直径0.28微米的嗜铬颗粒的表面积(0.25平方微米)相似。在表面斑点区域积分的平均荧光强度是嗜铬颗粒平均强度的25 - 30%,这一比例与已发表的嗜铬颗粒中40 - 50%的多巴胺β - 羟化酶与膜结合的值相似。斑点的表面密度与正在进行胞吐作用的颗粒数量一致。斑点没有聚集的趋势。这项工作的关键结论是,多巴胺β - 羟化酶的每个单独点状位点代表单个嗜铬颗粒的融合,并且多巴胺β - 羟化酶斑点在细胞表面的分布广泛且随机,这表明每个单独的颗粒与其自身的释放位点相关联。