Two pathways for insulin metabolism in adipocytes

被引:7
作者
Duckworth, WC
Hamel, FG
Peavy, DE
机构
[1] DEPT VET AFFAIRS MED CTR,MED RES SERV,OMAHA,NE
[2] INDIANA UNIV,SCH MED,DEPT MED,INDIANAPOLIS,IN
[3] DEPT VET AFFAIRS MED CTR,MED SERV,INDIANAPOLIS,IN
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 1997年 / 1358卷 / 02期
关键词
insulin degradation; adipocyte; inhibitor;
D O I
10.1016/S0167-4889(97)00066-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using selected conditions, the appropriate collagenase, albumin and cell treatment, a preparation of isolated adipocytes was developed with no extracellular insulin degrading activity. Cell mediated insulin degradation rates were 0.68% +/- 0.05%/100000 cell/h using trichloracetic acid precipitability as a measure. Chloroquine (CQ) increased cell-associated radioactivity and decreased degradation while dansylcadaverine (DC), PCMBS and bacitracin (BAC) decreased degradation with no effect on binding. Extraction and chromatography of the cell-associated radioactivity showed 3 peaks, a large molecular weight peak, a small molecular weight peak and an insulin-sized peak. CQ, DC and BAC all decreased the small molecular weight peak while CQ and DC also increased the peak of large molecular weight radioactivity. Cell mediated inhibitors of the insulin degrading enzyme (IDE) (bacitracin and PCMBS) and the other altered by cell processing inhibitors (DC, CQ and phenylarsenoxide), Chloroquine altered the pattern of the insulin-sized cell-associated HPLC assayed degradation products, further supporting two pathways of degradation; one a chloroquine-sensitive and one a chloroquine-insensitive pathway. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:163 / 171
页数:9
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