Disruption of a receptor-mediated mechanism for intracellular sorting of proinsulin in familial hyperproinsulinemia

被引:35
作者
Dhanvantari, S
Shen, FS
Adams, T
Snell, CR
Zhang, CF
Mackin, RB
Morris, SJ
Loh, YP
机构
[1] NICHHD, Cellular Neurobiol Sect, Dev Neurobiol Lab, NIH, Bethesda, MD 20892 USA
[2] Medivir UK Ltd, Cambridge CB1 9PT, England
[3] Creighton Univ, Sch Med, Omaha, NE 68178 USA
[4] McGill Univ, Montreal Neurol Inst, Montreal, PQ H3A 2B4, Canada
关键词
D O I
10.1210/me.2002-0380
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In familial hyperproinsulinemia, specific mutations in the proinsulin gene are linked with a profound increase in circulating plasma proinsulin levels. However, the molecular and cellular basis for this disease remains uncharacterized. Here we investigated how these mutations may disrupt the sorting signal required to target proinsulin to the secretory granules of the regulated secretory pathway, resulting in the unregulated release of proinsulin. Using a combination of molecular modeling and site-directed mutagenesis, we have identified structural molecular motifs in proinsulin that are necessary for correct sorting into secretory granules of endocrine cells. We show that membrane carboxypeptidase E (CPE), previously identified as a prohormone-sorting receptor, is essential for proinsulin sorting. This was demonstrated through short interfering RNA-mediated depletion of CPE and transfection with a dominant negative mutant of CPE in a beta-cell line. Mutant proinsulins found in familial hyperproinsulinemia failed to bind to CPE and were not sorted efficiently. These findings provide evidence that the elevation of plasma proinsulin levels found in patients with familial hyperproinsulinemia is caused by the disruption of CPE-mediated sorting of mutant proinsulins to the regulated secretory pathway.
引用
收藏
页码:1856 / 1867
页数:12
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