Abstract
To determine the effect of the tolerogenic peptide hCDR1 on hippocampal neurogenesis, we treated SLE-afflicted (NZBxNZW)F1 mice with hCDR1 (once a week for 10. weeks). The treatment resulted in the up-regulation of neurogenesis in the dentate gyrus and restored the NeuN immunoreactivity in brain hippocampi of the mice in association with increased gene expression of IGF-1, NGF and BDNF. Furthermore, hCDR1 treatment significantly up-regulated p-ERK and p-Akt that are suggested to be key components in mediating growth factor-induced neurogenesis. The observed effects of hCDR1 on hippocampal-neurogenesis and on associated signaling pathways suggest a potential role for hCDR1 in CNS lupus.
| Original language | English |
|---|---|
| Pages (from-to) | 151-157 |
| Number of pages | 7 |
| Journal | Journal of Neuroimmunology |
| Volume | 232 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - Mar 2011 |
| Externally published | Yes |
Keywords
- A model of systemic lupus erythematosus
- A tolerogenic peptide
- ERK and Akt pathways
- Growth and neurotrophic factors
- Hippocampal neurogenesis
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