Protein kinase C-dependent α-secretase competes with β-secretase for cleavage of amyloid-β precursor protein in the trans-Golgi network

被引：287
作者：
Skovronsky, DM [1 ]
Moore, DB [1 ]
Milla, ME [1 ]
Doms, RW [1 ]
Lee, VMY [1 ]
机构：
[1] Univ Penn, Sch Med, Ctr Neurodegenerat Dis Res, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
来源：
JOURNAL OF BIOLOGICAL CHEMISTRY | 2000年 / 275卷 / 04期
关键词：
D O I：
10.1074/jbc.275.4.2568
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：
The release of amyloidogenic amyloid-beta peptide (A beta) from amgloid-beta precursor protein (APP) requires cleavage by beta- and gamma-secretases. in contrast, alpha-secretase cleaves APP within the A beta sequence and precludes amyloidogenesis. Regulated and unregulated alpha-secretase activities have been reported, and the fraction of cellular alpha-secretase activity regulated by protein kinase C (PKC) has been attributed to the ADAM (a disintegrin and metalloproaease) family members TACE and ADAM-10. Although unregulated alpha-secretase cleavage of APP has been shown to occur at the cell surface, we sought to identify the intracellular site of PEG-regulated alpha-secretase APP cleavage. To accomplish this, we measured levels of secreted ectodomains and C-terminal fragments of APP generated by alpha-secretase (sAPP alpha) (C83) versus beta-secretase (sAPP beta) (C99) and secreted A beta in cultured cells treated with PEC and inhibitors of TACE/ ADAM-10. We found that PKC stimulation increased sAPP alpha but decreased sAPP beta levels by altering the competition between alpha- versus beta-secretase for APP within the same organelle rather than by perturbing APP trafficking. Moreover, data implicating the trans-Golgi network (TGN) as a major site for beta-secretase activity prompted us to hypothesize that PEG-regulated alpha-secretase(s) also reside in this organelle, To test this hypothesis, we performed studies demonstrating proteolytically mature TACE intracellularly, and we also showed that regulated alpha-secretase APP cleavage occurs in the TGN using an APP mutant construct targeted specifically to the TGN, By detecting regulated alpha-secretase APP cleavage in the TGN by TACE/ADAM-10, we reveal ADAM activity in a novel location. Finally, the competition between TACE/ADAM-10 and beta-secretase for intracellular APP cleavage may represent a novel target for the discovery of new therapeutic agents to treat Alzheimer's disease.
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页码：2568 / 2575
页数：8
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