Effect of Truncated-ApoE4 Overexpression on tau Phosphorylation in Cultured N2a Cells
- Author:
Jie ZHOU
1
;
Juan CHEN
;
Youmei FENG
Author Information
1. 华中科技大学同济医学院
- Keywords:
truncated-ApoE4;
tau;
glycogen synthase kinase-3;
Alzheimer disease
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2006;26(3):272-274
- CountryChina
- Language:Chinese
-
Abstract:
The carboxyl-terminal amino acids 272-299-truncated apoE4 (△272-299) is the main fragments of apoE4 hydrolysate in neurons. The effects of truncated-ApoE4 (△272-299) overexpression on tau phosphorylation in cultured N2a cells were investigated. The truncated-apoE4 (△272-299)cDNA was subcloned into pEGFP-c3 to form recombinant pEGFP-T-apoE4. pEGFP-c3, pEGFP-TapoE4 and pEGFP-apoE4 were transfected into N2a cells respectively by lipofectamine 2000 method. After 24-48 h, tau phosphorylation was detected by Western blot assay and glycogen synthase kinase-3 (GSK-3) activity by using GSK-3 activity assay. The results showed that the overexpression of both full length-apoE4 and truncated apoE4 fragments in N2a cells induced a dramatic increase in phosphorylation of tau at Ser202 sites and the activation of GSK-3 as compared with untransfected cells, most significantly in the cells transfected with pEGFP-T-apoE4 (P＜0.05). It was concluded that in vitro overexpression of truncated-ApoE4 (△272-299) can result in tau hyperphosphorylation in N2a cells by activating GSK-3, suggesting truncated-ApoE4 (△272-299) might contribute the pathogenesis of Alzheimer disease.
