Acetylcholinesterase Modulates Neurite Outgrowth on Fibronectin.
From: Dipartimento Biologia Cellulare e Sviluppo, Università La Sapienza, Piazzale A. Moro 5, 00185 Roma, Italy.
Biochemical and biophysical research communications
- Publish Date: May 2007
- ISSN: 0006-291X
- Volume: 356
- Issue: 2
- Pages: 398-404
- Medium: Print
- Language: English
- Citation (JAMA): Giordano C, Poiana G, Augusti-Tocco G, et al. Acetylcholinesterase Modulates Neurite Outgrowth on Fibronectin.. Biochem. Biophys. Res. Commun. May 2007;356:398-404
Abstract
Acetylcholinesterase (AChE) has been reported to be involved in the modulation of neurite outgrowth. To understand the role played by different domains, we transfected neuroblastoma cells with three constructs containing the invariant region of AChE, differing in the exon encoding the C-terminus and therefore in AChE cellular fate and localization. All isoforms increased neurite extension, suggesting the involvement of the invariant domain [A. De Jaco, G. Augusti-Tocco, S. Biagioni, Alternative AChE molecular forms exhibit similar ability to induce neurite outgrowth, J. Neurosci. Res. 70 (2002) 756-765]. The peripheral anionic site (PAS) is encoded by invariant exons and represents the domain involved in non-cholinergic functions of AChE. Masking of PAS with fasciculin results in a significant decrease of neurite outgrowth in all clones overexpressing AChE. A strong reduction was also observed when clones were cultured on fibronectin. Treatment of clones with fasciculin, therefore masking PAS, abolished the fibronectin-induced reduction. The inhibition of the catalytic site cannot revert the fibronectin effect. Finally, when clones were cultured on fibronectin in the presence of heparin, a ligand of fibronectin, the inhibitory effect was completely reversed. Our results indicate that PAS could directly or indirectly mediate AChE/fibronectin interactions.
Mesh Headings (Keywords): Acetylcholinesterase, Animals, Cholinesterase Inhibitors, Fibronectins, Mice, Neurites, Tumor Cells, Cultured
Check for Full Text / PubMed Unique Identifier (PMID): 17359933
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