Abstract
We investigated the regulation of primary neurite growth and expression of specific growth-associated genes by lens epithelium-derived growth factor (LEDGF) in rat retinal ganglion cells (RGCs). A pAd-LEDGFp52 adenovirus vector and a siRNA-LEDGFp52 eucaryotic expression vector were transfected into cultured RGCs. Iransfection with pAd-LEDGFp52 significantly increased the number of neurites and their lengths compared with untransfected control RGCs. The expression of growth associated protein 43 (GAP43), microtubule-associated protein 2 (MAP2), and low-molecular-weight neurofilament (NF-L) genes and proteins were also significantly up-regulated. In contrast, the introduction of siRNA-LEDGFp52 significantly decreased the number and length of neurites, and significantly down-regulated the expression GAP43, NF-L and MAP2 genes and proteins compared with controls. Our findings suggest that LEDGFp52 might act as a dendritic arborization gene as well as an axonal elongation gene in RGCs and that it might be beneficial to the functional recovery of regenerating RGCs.
Original language | English |
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Pages (from-to) | 815-829 |
Number of pages | 15 |
Journal | Journal of International Medical Research |
Volume | 36 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2008 |
Externally published | Yes |
Keywords
- Gene regulation
- Growth associated protein 43 (GAP43)
- Lens epithelium-derived growth factor (LEDGF)
- Low-molecular-weight neurofilament (NF-L)
- Microtubule-associated protein 2 (MAP2)
- Neuronal growth
- Protein regulation
- Retinal ganglion cells (RGCS)