Journal
CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 34, Issue 3, Pages 409-417Publisher
SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-014-0026-0
Keywords
Neural stem/progenitor cells; RhoC; A beta(42); Migration
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Funding
- National Natural Science Fund [81270432]
- Polytechnic crossover Foundation of Shanghai Jiao Tong University [AE1700003]
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Alzheimer's disease (AD) is characterized by deposition of beta-amyloid peptides (A beta) and progressive loss of neurons. Neural stem/progenitor cells (NSPCs) can proliferate and produce immature neurons even in the brain of AD patients. However, A beta(42) significantly decreased the expression of RhoC in NSPCs during the co-incubation (P < 0.01). Treating with RhoC siRNA prevented membrane from protrusion and led to a significant reduction in cell migration in responses to SDF-1. Compared with wild-type mice, the numbers of RhoC-immunoreactive cells in hippocampus and cortex were significantly down-regulated in APP/PS1 mice aged 9 months. The results suggest that A beta(42) down-regulates the expression of RhoC in NSPCs in vitro and in vivo; down-regulated RhoC expression results in decreased migration of NSPCs.
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