Expression of glycogenes in differentiating human NT2N neurons. Downregulation of fucosyltransferase 9 leads to decreased Lewisx levels and impaired neurite outgrowth

Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the central nervous system. Here we have analysed the glycogene expression and glycosylation patterns during human NT2N neuron differentiation. We have further stu...

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Published inBiochimica et biophysica acta. General subjects Vol. 1820; no. 12; pp. 2007 - 2019
Main Authors Gouveia, Ricardo, Schaffer, Lana, Papp, Suzanne, Grammel, Nicolas, Kandzia, Sebastian, Head, Steven R., Kleene, Ralf, Schachner, Melitta, Conradt, Harald S., Costa, Júlia
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.12.2012
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Abstract Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the central nervous system. Here we have analysed the glycogene expression and glycosylation patterns during human NT2N neuron differentiation. We have further studied the impact of downregulating fucosyltransferase 9 (FUT9) on neurite outgrowth. The expression of glycogenes in human NT2N neurons differentiating from teratocarcinoma NTERA-2/cl.D1 cells has been analysed using the GlycoV4 GeneChip expression microarray. Changes in glycosylation have been monitored by immunoblot, immunofluorescence microscopy, HPLC and MALDI-TOF MS. Peptide mass fingerprinting and immunoprecipitation have been used for protein identification. FUT9 was downregulated using silencing RNA. One hundred twelve mRNA transcripts showed statistically significant up-regulation, including the genes coding for proteins involved in the synthesis of the Lewisx motif (FUT9), polysialic acid (ST8SIA2 and ST8SIA4) and HNK-1 (B3GAT2). Accordingly, increased levels of the corresponding carbohydrate epitopes have been observed. The Lewisx structure was found in a carrier glycoprotein that was identified as the CRA-a isoform of human neural cell adhesion molecule 1. Downregulation of FUT9 caused significant decreases in the levels of Lewisx, as well as GAP-43, a marker of neurite outgrowth. Concomitantly, a reduction in neurite formation and outgrowth has been observed that was reversed by FUT9 overexpression. These results provided information about the regulation of glycogenes during neuron differentiation and they showed that the Lewisx motif plays a functional role in neurite outgrowth from human neurons. ► Changes in glycogene expression were found during NT2N neuron differentiation. ► Increase in FUT9 expression that encodes the enzyme synthesizing Lewisx was observed. ► NCAM is the predominant glycoprotein carrier of Lewisx in NT2N neurons. ► Downregulation of FUT9 caused decreased Lewisx levels and impaired neurite outgrowth.
AbstractList Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the central nervous system. Here we have analysed the glycogene expression and glycosylation patterns during human NT2N neuron differentiation. We have further studied the impact of downregulating fucosyltransferase 9 (FUT9) on neurite outgrowth. The expression of glycogenes in human NT2N neurons differentiating from teratocarcinoma NTERA-2/cl.D1 cells has been analysed using the GlycoV4 GeneChip expression microarray. Changes in glycosylation have been monitored by immunoblot, immunofluorescence microscopy, HPLC and MALDI-TOF MS. Peptide mass fingerprinting and immunoprecipitation have been used for protein identification. FUT9 was downregulated using silencing RNA. One hundred twelve mRNA transcripts showed statistically significant up-regulation, including the genes coding for proteins involved in the synthesis of the Lewisx motif (FUT9), polysialic acid (ST8SIA2 and ST8SIA4) and HNK-1 (B3GAT2). Accordingly, increased levels of the corresponding carbohydrate epitopes have been observed. The Lewisx structure was found in a carrier glycoprotein that was identified as the CRA-a isoform of human neural cell adhesion molecule 1. Downregulation of FUT9 caused significant decreases in the levels of Lewisx, as well as GAP-43, a marker of neurite outgrowth. Concomitantly, a reduction in neurite formation and outgrowth has been observed that was reversed by FUT9 overexpression. These results provided information about the regulation of glycogenes during neuron differentiation and they showed that the Lewisx motif plays a functional role in neurite outgrowth from human neurons. ► Changes in glycogene expression were found during NT2N neuron differentiation. ► Increase in FUT9 expression that encodes the enzyme synthesizing Lewisx was observed. ► NCAM is the predominant glycoprotein carrier of Lewisx in NT2N neurons. ► Downregulation of FUT9 caused decreased Lewisx levels and impaired neurite outgrowth.
BACKGROUND: Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the central nervous system. Here we have analysed the glycogene expression and glycosylation patterns during human NT2N neuron differentiation. We have further studied the impact of downregulating fucosyltransferase 9 (FUT9) on neurite outgrowth. METHODS: The expression of glycogenes in human NT2N neurons differentiating from teratocarcinoma NTERA-2/cl.D1 cells has been analysed using the GlycoV4 GeneChip expression microarray. Changes in glycosylation have been monitored by immunoblot, immunofluorescence microscopy, HPLC and MALDI-TOF MS. Peptide mass fingerprinting and immunoprecipitation have been used for protein identification. FUT9 was downregulated using silencing RNA. RESULTS AND CONCLUSIONS: One hundred twelve mRNA transcripts showed statistically significant up-regulation, including the genes coding for proteins involved in the synthesis of the Lewisˣ motif (FUT9), polysialic acid (ST8SIA2 and ST8SIA4) and HNK-1 (B3GAT2). Accordingly, increased levels of the corresponding carbohydrate epitopes have been observed. The Lewisˣ structure was found in a carrier glycoprotein that was identified as the CRA-a isoform of human neural cell adhesion molecule 1. Downregulation of FUT9 caused significant decreases in the levels of Lewisˣ, as well as GAP-43, a marker of neurite outgrowth. Concomitantly, a reduction in neurite formation and outgrowth has been observed that was reversed by FUT9 overexpression. GENERAL SIGNIFICANCE: These results provided information about the regulation of glycogenes during neuron differentiation and they showed that the Lewisˣ motif plays a functional role in neurite outgrowth from human neurons.
Author Kleene, Ralf
Schachner, Melitta
Costa, Júlia
Schaffer, Lana
Head, Steven R.
Gouveia, Ricardo
Kandzia, Sebastian
Papp, Suzanne
Grammel, Nicolas
Conradt, Harald S.
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  givenname: Melitta
  surname: Schachner
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  givenname: Harald S.
  surname: Conradt
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  givenname: Júlia
  surname: Costa
  fullname: Costa, Júlia
  email: jcosta@itqb.unl.pt
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Keywords PBS
TBS
HRP
Lewisx
PNGase F
HPAEC-PAD
EDTA
EGTA
BSA
MALDI-TOF MS
SDS-PAGE
HNK-1
Gal
Fuc
HexNAc
Neuronal differentiation
dHex
Fucosyltransferase 9
GlcNAc
Hex
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Neuron glycosylation
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Snippet Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the central nervous...
BACKGROUND: Several glycan structures are functionally relevant in biological events associated with differentiation and regeneration which occur in the...
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SubjectTerms carbohydrates
cell adhesion
cells
Central nervous system
epitopes
fluorescence microscopy
Fucosyltransferase 9
genes
glycoproteins
glycosylation
high performance liquid chromatography
HPLC
humans
immunofluorescence
Lewisx
messenger RNA
microarray technology
microscopy
Neurite outgrowth
Neuron glycosylation
Neuronal differentiation
neurons
peptides
precipitin tests
proteins
regulations
RNA interference
Title Expression of glycogenes in differentiating human NT2N neurons. Downregulation of fucosyltransferase 9 leads to decreased Lewisx levels and impaired neurite outgrowth
URI https://dx.doi.org/10.1016/j.bbagen.2012.09.004
https://www.proquest.com/docview/2000032658
Volume 1820
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