Increased levels of fucosyltransferase IX and carbohydrate Lewisx adhesion determinant in human NT2N neurons
✍ Scribed by Catarina Brito; Cristina Escrevente; Celso A. Reis; Virginia M.-Y. Lee; John Q. Trojanowski; Júlia Costa
- Book ID
- 102907463
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 778 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
The expression of the fucosylated carbohydrate Lewis^x^ (Le^x^) determinant (Gal(β1–4)[Fuc(α1–3)]GlcNAc‐R) has been found in glycoproteins, proteoglycans, and glycolipids from the nervous system. Evidence suggests its association with cell–cell recognition, neurite outgrowth, and neuronal migration during central nervous system development. In the present work, we detected increased levels of Le^x^ in differentiated human NT2N neurons cultured in vitro. To identify which fucosyltransferase (FUT) synthesized the Le^x^ in NT2N neurons, RT‐PCR, FUT substrate specificity and Western blot analysis were carried out. Strong activity toward acceptors Galβ4GlcNAc‐O‐R and Fucα2Galβ4GlcNAc‐O‐R [R = ‐(CH~2~)~3~NHCO(CH~2~)~5~NH‐biotin], together with strong FUT9 detection by Western blot and presence of transcripts showed that FUT9 was the enzyme associated with Le^x^ biosynthesis in NT2N neurons. Le^x^ was detected at the plasma membrane of NT2N neurons, in lysosomes marked with lysosomal‐associated membrane protein 1 (LAMP‐1), and it was found for the first time to colocalize with the tetanus neurotoxin‐insensitive vesicle‐associated membrane protein (TI‐VAMP) that defines the TI‐VAMP exocytic compartment that is involved in neurite outgrowth. Furthermore, incubation with anti‐Le^x^ monoclonal antibody L5 led to impaired adhesion of NT2N neurons to the surface matrix and inhibited neurite initiation. In conclusion, FUT9 and its product Le^x^ are detected specifically in human NT2N neurons and our results indicate that they underlie cell differentiation, cell adhesion, and initiation of neurite outgrowth in those neurons. © 2007 Wiley‐Liss, Inc.