Upregulation of neuronal astrocyte elevated gene-1 protects nigral dopaminergic neurons in vivo
- Authors
- Leem, Eunju; Kim, Hyung-Jun; Choi, Minji; Kim, Sehwan; Oh, Yong-Seok; Lee, Kea Joo; Choe, Young-Shik; Um, Jae-Young; Shin, Won-Ho; Jeong, Jae Yeong; Jin, Byung Kwan; Kim, Dong Woon; McLean, Catriona; Fisher, Paul B.; Kholodilov, Nikolai; Ahn, Kwang Seok; Lee, Jae Man; Jung, Un Ju; Lee, Seok-Geun; Kim, Sang Ryong
- Issue Date
- Apr-2018
- Publisher
- NATURE PUBLISHING GROUP
- Citation
- CELL DEATH & DISEASE, v.9
- Journal Title
- CELL DEATH & DISEASE
- Volume
- 9
- URI
- http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/743
- DOI
- 10.1038/s41419-018-0491-3
- ISSN
- 2041-4889
- Abstract
- The role of astrocyte elevated gene-1 (AEG-1) in nigral dopaminergic (DA) neurons has not been studied. Here we report that the expression of AEG-1 was significantly lower in DA neurons in the postmortem substantia nigra of patients with Parkinson's disease (PD) compared to age-matched controls. Similarly, decreased AEG-1 levels were found in the 6-hydroxydopamine (6-OHDA) mouse model of PD. An adeno-associated virus-induced increase in the expression of AEG-1 attenuated the 6-OHDA-triggered apoptotic death of nigral DA neurons. Moreover, the neuroprotection conferred by the AEG-1 upregulation significantly intensified the neurorestorative effects of the constitutively active ras homolog enriched in the brain [Rheb(S16H)]. Collectively, these results demonstrated that the sustained level of AEG-1 as an important anti-apoptotic factor in nigral DA neurons might potentiate the therapeutic effects of treatments, such as Rheb(S16H) administration, on the degeneration of the DA pathway that characterizes PD.
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