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Imaging specific cellular glycan structures using glycosyltransferases via click chemistry
Heparan sulfate (HS) is a polysaccharide fundamentally important for biologically activities. T/Tn antigens are universal carbohydrate cancer markers. Here, we report the specific imaging of these carbohydrates using a mesenchymal stem cell line and human umbilical vein endothelial cells (HUVEC). Th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993098/ https://www.ncbi.nlm.nih.gov/pubmed/29186441 http://dx.doi.org/10.1093/glycob/cwx095 |
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author | Wu, Zhengliang L Person, Anthony D Anderson, Matthew Burroughs, Barbara Tatge, Timothy Khatri, Kshitij Zou, Yonglong Wang, Lianchun Geders, Todd Zaia, Joseph Sackstein, Robert |
author_facet | Wu, Zhengliang L Person, Anthony D Anderson, Matthew Burroughs, Barbara Tatge, Timothy Khatri, Kshitij Zou, Yonglong Wang, Lianchun Geders, Todd Zaia, Joseph Sackstein, Robert |
author_sort | Wu, Zhengliang L |
collection | PubMed |
description | Heparan sulfate (HS) is a polysaccharide fundamentally important for biologically activities. T/Tn antigens are universal carbohydrate cancer markers. Here, we report the specific imaging of these carbohydrates using a mesenchymal stem cell line and human umbilical vein endothelial cells (HUVEC). The staining specificities were demonstrated by comparing imaging of different glycans and validated by either removal of target glycans, which results in loss of signal, or installation of target glycans, which results in gain of signal. As controls, representative key glycans including O-GlcNAc, lactosaminyl glycans and hyaluronan were also imaged. HS staining revealed novel architectural features of the extracellular matrix (ECM) of HUVEC cells. Results from T/Tn antigen staining suggest that O-GalNAcylation is a rate-limiting step for O-glycan synthesis. Overall, these highly specific approaches for HS and T/Tn antigen imaging should greatly facilitate the detection and functional characterization of these biologically important glycans. |
format | Online Article Text |
id | pubmed-5993098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59930982018-06-13 Imaging specific cellular glycan structures using glycosyltransferases via click chemistry Wu, Zhengliang L Person, Anthony D Anderson, Matthew Burroughs, Barbara Tatge, Timothy Khatri, Kshitij Zou, Yonglong Wang, Lianchun Geders, Todd Zaia, Joseph Sackstein, Robert Glycobiology Regular Manuscripts Heparan sulfate (HS) is a polysaccharide fundamentally important for biologically activities. T/Tn antigens are universal carbohydrate cancer markers. Here, we report the specific imaging of these carbohydrates using a mesenchymal stem cell line and human umbilical vein endothelial cells (HUVEC). The staining specificities were demonstrated by comparing imaging of different glycans and validated by either removal of target glycans, which results in loss of signal, or installation of target glycans, which results in gain of signal. As controls, representative key glycans including O-GlcNAc, lactosaminyl glycans and hyaluronan were also imaged. HS staining revealed novel architectural features of the extracellular matrix (ECM) of HUVEC cells. Results from T/Tn antigen staining suggest that O-GalNAcylation is a rate-limiting step for O-glycan synthesis. Overall, these highly specific approaches for HS and T/Tn antigen imaging should greatly facilitate the detection and functional characterization of these biologically important glycans. Oxford University Press 2017-12-22 /pmc/articles/PMC5993098/ /pubmed/29186441 http://dx.doi.org/10.1093/glycob/cwx095 Text en © The Author(s) 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Regular Manuscripts Wu, Zhengliang L Person, Anthony D Anderson, Matthew Burroughs, Barbara Tatge, Timothy Khatri, Kshitij Zou, Yonglong Wang, Lianchun Geders, Todd Zaia, Joseph Sackstein, Robert Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title | Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title_full | Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title_fullStr | Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title_full_unstemmed | Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title_short | Imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
title_sort | imaging specific cellular glycan structures using glycosyltransferases via click chemistry |
topic | Regular Manuscripts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993098/ https://www.ncbi.nlm.nih.gov/pubmed/29186441 http://dx.doi.org/10.1093/glycob/cwx095 |
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