4.7 Article

RanBP9 aggravates synaptic damage in the mouse brain and is inversely correlated to spinophilin levels in Alzheimer's brain synaptosomes

期刊

CELL DEATH & DISEASE
卷 4, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/cddis.2013.183

关键词

RanBP9; spinophilin; transgenic mice; synaptosomes; spines; mitochondrial activity

资金

  1. National Institute of Aging (NIA)/NIH [1R03AG032064-01, 1R01AG036859-01]
  2. PHS at the McLean Hospital [R24MH068855]
  3. Harvard Brain Tissue Resource Center

向作者/读者索取更多资源

We previously demonstrated that overexpression of RanBP9 led to enhanced A beta generation in a variety of cell lines and primary neuronal cultures, and subsequently, we confirmed increased amyloid plaque burden in a mouse model of Alzheimer's disease (AD). In the present study, we found striking reduction of spinophilin protein levels when RanBP9 is overexpressed. At 12 months of age, we found spinophilin levels reduced by 70% (P<0.001) in the cortex of AP Delta E9/RanBP9 mice compared with that in wild-type (WT) controls. In the hippocampus, the spinophilin levels were reduced by 45% (P<0.01) in the APDE9/RanBP9 mice. Spinophilin immunoreactivity was also reduced by 22% (P<0.01) and 12% (P<0.05) in the cortex of AP Delta E9/RanBP9 and AP Delta E9 mice, respectively. In the hippocampus, the reductions were 27% (P<0.001) and 14% (P<0.001) in the AP Delta E9/RanBP9 and AP Delta E9 mice, respectively. However, in the cerebellum, spinophilin levels were not altered in either AP Delta E9 or AP Delta E9/RanBP9 mice. Additionally, synaptosomal functional integrity was reduced under basal conditions by 39% (P<0.001) in the AP Delta E9/RanBP9 mice and similar to 23% (P<0.001) in the AP Delta E9 mice compared with that in WT controls. Under ATP- and KCl-stimulated conditions, we observed higher mitochondrial activity in the WT and AP Delta E9 mice, but lower in the AP Delta E9/RanBP9 mice. Significantly, we confirmed the inverse relationship between RanBP9-N60 and spinophilin in the synaptosomes of Alzheimer's brains. More importantly, both AP Delta E9 and AP Delta E9/RanBP9 mice showed impaired learning and memory skills compared to WT controls. These data suggest that RanBP9 might play a crucial role in the loss of spines and synapses in AD.

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