Rapid insulin-induced exocytosis in white rat adipocytes

被引:9
|
作者
Chowdbury, HH
Kreft, M
Zorec, R
机构
[1] Univ Ljubljana, Sch Med, Inst Pathophysiol, Lab Neuroendocrinol Mol Cell Physiol, Ljubljana 1000, Slovenia
[2] Celica Biomed Sci Ctr, Ljubljana 1000, Slovenia
来源
关键词
confocal microscopy; FM1-43; insulin; exocytosis; white adipocytes;
D O I
10.1007/s00424-002-0938-2
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Insulin is believed to increase glucose permeability of adipocytes by regulating the incorporation of glucose transporters into the plasma membrane by exocytosis. This process involves fusion of membrane-bound cellular compartments with the plasma membrane, thus influencing the plasma membrane area. However, insulin-induced changes in plasma membrane area have not yet been demonstrated. In the present study we monitored fluorescence intensity with a confocal microscope to study the effect of insulin on adipocyte plasma membrane area. After cell isolation and adhesion to a glass cover-slip, adipocytes were stained with the dye FM1-43, a membrane area reporter. At rest, the rate of fluorescence intensity increase was initially high, but gradually stabilized at 2%/min. This steady increase in fluorescence is due to a slow rate of exocytosis coupled to endocytosis, since the removal of FM1-43 from the bath did not abolish FM1-43 fluorescence. Insulin addition caused an abrupt increase of fluorescence intensity of 4%/ min, which was significantly higher than in controls. These results suggest rapid, insulin-induced incorporation of new membrane into the plasma membrane by exocytosis.
引用
收藏
页码:352 / 356
页数:5
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