Guanosine protects SH-SYSY cells against β-amyloid-induced apoptosis

被引:43
作者
Pettifer, KM
Kleywegt, S
Bau, CJ
Ramsbottom, JD
Vertes, E
Ciccarelli, R
Caciagli, F
Werstiuk, ES
Rathbone, MP
机构
[1] McMaster Univ, Hlth Sci Ctr, Dept Med, Hamilton, ON L8N 3Z5, Canada
[2] Univ G dAnnunzio, Sch Med, Dept Biomed Sci, I-66013 Chieti, Italy
[3] Univ Trieste, Dept Biomed Sci, I-34127 Trieste, Italy
关键词
apoptosis; Alzheimer's disease; beta-amyloid; cell survival; guanosine; SH-SY5Y neuroblastoma cells PI3K/Akt/PKB; MAPK;
D O I
10.1097/00001756-200404090-00019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Apoptosis is implicated in the pathophysiology of Alzheimer's disease. Extracellular guanosine inhibits staurosporine-induced apoptosis in astrocytes. We examined whether guanosine protects SH-SY5Y human neuroblastoma cells against beta-amyloid (betaA)-induced apoptosis. Addition of betaA (fragment 25-35, 5 muM for 24 h) to SH-SY5Y cells increased the number of apoptotic cells, as evaluated by oligonucleosome ELISA. Guanosine pre-treatment decreased betaA-induced apoptosis (maximal effect after 24 h, 300 muM, p < 0.05). The anti-apoptotic effect of guanosine was reduced by LY294002 (PI3K inhibitor) or PD98059 (MEK inhibitor) (p < 0.05). Guanosine increased phosphorylation of Akt/PKB, and this was abolished by inhibiting PI3K or MEK, (p < 0.001, 5 min). Thus, the protective effect of guanosine against beta A-induced apoptosis of SH-SY5Y cells is mediated via activation of the PI3K/Akt/PKB and MAPK pathways.
引用
收藏
页码:833 / 836
页数:4
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