LEDGFp52 controls rat retinal ganglion cell neurite growth in culture and regulates specific neuronal growth-associated genes and protein production

H. S. Zhao, S. J. Chen, N. Wu, X. Q. Wang, Z. Q. Yin, Y. Wang*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

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 languageEnglish
Pages (from-to)815-829
Number of pages15
JournalJournal of International Medical Research
Volume36
Issue number4
DOIs
Publication statusPublished - 2008
Externally publishedYes

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)

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