Cation selective channels formed by a C-terminal fragment of β-amyloid precursor protein

被引:21
作者
Kim, HJ
Suh, YH
Lee, MH
Ryu, PD
机构
[1] Seoul Natl Univ, Coll Vet Med, Dept Pharmacol, Suwon 441744, South Korea
[2] Seoul Natl Univ, Coll Vet Med, Dept Biochem, Suwon 441744, South Korea
[3] Seoul Natl Univ, Neurosci Res Inst MRC, Suwon 441744, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
[5] Seoul Natl Univ, Neurosci Res Inst MRC, Seoul 110799, South Korea
关键词
Alzheimer's disease; amyloid beta-precursor protein; C-terminal fragment; cation selective; ion channels; planar lipid bilayer;
D O I
10.1097/00001756-199905140-00008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE C-terminal 105 amino acid fragment of beta-amyloid precursor protein (CT105) is highly neurotoxic. To obtain insights into its cytotoxic effect, we examined the ionophoric effects of CT105 (10-1000 nM) on artificial lipid membranes. Macroscopic membrane conductance increased with CT105 concentration and its ionophoric effect Tvas comparable to that of amyloid beta protein. The mean unitary conductance of CT105-induced channels was 120 pS and open-state probability was close to 1 at voltages from -80 to +80 mV. CT105-induced channels were selective to cations (P-K/ P-Cl = 10.2), being most selective to Ca2+. These findings suggest that CT105 can cause direct neurotoxic effects by forming Ca2+ permeable cation channels on neuronal membranes. NeuroReport 10:1427-1431 (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:1427 / 1431
页数:5
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