| First Author | Segev Y | Year | 2013 |
| Journal | Neurobiol Aging | Volume | 34 |
| Issue | 3 | Pages | 863-72 |
| PubMed ID | 22883908 | Mgi Jnum | J:194428 |
| Mgi Id | MGI:5473757 | Doi | 10.1016/j.neurobiolaging.2012.06.020 |
| Citation | Segev Y, et al. (2013) ApoE epsilon4 is associated with eIF2alpha phosphorylation and impaired learning in young mice. Neurobiol Aging 34(3):863-72 |
| abstractText | Protein translation is regulated during both initiation and elongation phases to enable cells to accommodate for ever-changing environmental and internal states. Eukaryotic initiation factor-2 (eIF2)alpha, a major signaling pathway for responses to metabolic stress, controls translation initiation in various cells, including neurons, and affects cognitive functions. The main risk factor for sporadic Alzheimer's disease (SAD) is aging, and the main genetic risk factor reducing the age of SAD onset is the expression of apolipoprotein E (ApoE)4. We tested the hypothesis that both genetic and aging risk factors converge on the eIF2alpha pathway. Aged rodents showed increased eIF2alpha phosphorylation in the brain, indicating a shift in the rate of translation initiation with increasing age. Interestingly, mice overexpressing human ApoE4 already, at an early age, exhibited increased eIF2alpha phosphorylation together with mild impairment in cognitive tasks, compared with ApoE3 mice. These results suggest that the eIF2alpha pathway is linked to SAD, possibly via genetic as well as prolonged metabolic stress, and these findings position it as a new and important target for treatment of the currently incurable Alzheimer's disease. |
