4.3 Article

Downregulated AEG-1 together with inhibited PI3K/Akt pathway is associated with reduced viability of motor neurons in an ALS model

期刊

MOLECULAR AND CELLULAR NEUROSCIENCE
卷 68, 期 -, 页码 303-313

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2015.08.009

关键词

Amyotrophic lateral sclerosis (ALS); Astrocyte elevated gene-1 (AEG-1); CREB; PI3K/Akt pathway

资金

  1. Natural Science Foundation of China [81171186]
  2. Major Program of Natural Science Foundation of Heilongjiang Province of China [ZD201417]
  3. Health Department Project of Heilongjiang Province [2013017]
  4. Intramural Research Program of the National Institute of Mental Health National Institutes of Health (IRP-NIMH-NIH) of the USA

向作者/读者索取更多资源

Astrocyte elevated gene-1 (AEG-1) has been reported to regulate the phosphatidylinositol 3-kinase (PI3K)/Akt pathway and is also regulated by it. This study investigated how AEG-1 participates in the survival pathway of motor neurons in amyotrophic lateral sclerosis (ALS). We found reduced levels of AEG-1 in ALS motor neurons, both in vivo and in vitro, compared to wild type controls. Moreover, AEG-1 silencing demonstrated inhibition of the PI3K/Akt pathway and increased cell apoptosis. Additionally, the PI3K/Akt pathway in mSOD1 cells was unresponsive under serum deprivation conditions compared to wtSOD1 cells. These results suggest that AEG-1 deficiency, together with the inhibited PI3K/Akt pathway was associated with decreased viability of ALS motor neurons. However, the mRNA levels of AEG-1 were still lower in mSOD1 cells compared to the control groups, though the signaling pathway was activated by application of a PI3-K activator. This suggests that in ALS motor neurons, some unknown interruption exists in the PI3K/Akt/CREB/AEG-1 feedback loop, thus attenuating the protection by this signaling pathway. Together, these findings support that AEG-1 is a critical factor for cell survival, and the disrupted PI3K/Akt/CREB/AEG-1 cycle is involved in the death of injured motor neurons and pathogenesis of ALS. (C) 2015 Elsevier Inc. All rights reserved.

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