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A novel cytoskeletal action of xylosides

Proteoglycan glycosaminoglycan (GAG) chains are attached to a serine residue in the protein through a linkage series of sugars, the first of which is xylose. Xylosides are chemicals which compete with the xylose at the enzyme xylosyl transferase to prevent the attachment of GAG chains to proteins. T...

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Autores principales: Mencio, Caitlin P., Tilve, Sharada M., Suzuki, Masato, Higashi, Kohei, Katagiri, Yasuhiro, Geller, Herbert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239447/
https://www.ncbi.nlm.nih.gov/pubmed/35763520
http://dx.doi.org/10.1371/journal.pone.0269972
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author Mencio, Caitlin P.
Tilve, Sharada M.
Suzuki, Masato
Higashi, Kohei
Katagiri, Yasuhiro
Geller, Herbert M.
author_facet Mencio, Caitlin P.
Tilve, Sharada M.
Suzuki, Masato
Higashi, Kohei
Katagiri, Yasuhiro
Geller, Herbert M.
author_sort Mencio, Caitlin P.
collection PubMed
description Proteoglycan glycosaminoglycan (GAG) chains are attached to a serine residue in the protein through a linkage series of sugars, the first of which is xylose. Xylosides are chemicals which compete with the xylose at the enzyme xylosyl transferase to prevent the attachment of GAG chains to proteins. These compounds have been employed at concentrations in the millimolar range as tools to study the role of GAG chains in proteoglycan function. In the course of our studies with xylosides, we conducted a dose-response curve for xyloside actions on neural cells. To our surprise, we found that concentrations of xylosides in the nanomolar to micromolar range had major effects on cell morphology of hippocampal neurons as well as of Neuro2a cells, affecting both actin and tubulin cytoskeletal dynamics. Such effects/morphological changes were not observed with higher xyloside concentrations. We found a dose-dependent alteration of GAG secretion by Neuro2a cells; however, concentrations of xylosides which were effective in altering neuronal morphology did not cause a large change in the rate of GAG chain secretion. In contrast, both low and high concentrations of xylosides altered HS and CS composition. RNAseq of treated cells demonstrated alterations in gene expression only after treatment with millimolar concentration of xylosides that had no effect on cell morphology. These observations support a novel action of xylosides on neuronal cells.
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spelling pubmed-92394472022-06-29 A novel cytoskeletal action of xylosides Mencio, Caitlin P. Tilve, Sharada M. Suzuki, Masato Higashi, Kohei Katagiri, Yasuhiro Geller, Herbert M. PLoS One Research Article Proteoglycan glycosaminoglycan (GAG) chains are attached to a serine residue in the protein through a linkage series of sugars, the first of which is xylose. Xylosides are chemicals which compete with the xylose at the enzyme xylosyl transferase to prevent the attachment of GAG chains to proteins. These compounds have been employed at concentrations in the millimolar range as tools to study the role of GAG chains in proteoglycan function. In the course of our studies with xylosides, we conducted a dose-response curve for xyloside actions on neural cells. To our surprise, we found that concentrations of xylosides in the nanomolar to micromolar range had major effects on cell morphology of hippocampal neurons as well as of Neuro2a cells, affecting both actin and tubulin cytoskeletal dynamics. Such effects/morphological changes were not observed with higher xyloside concentrations. We found a dose-dependent alteration of GAG secretion by Neuro2a cells; however, concentrations of xylosides which were effective in altering neuronal morphology did not cause a large change in the rate of GAG chain secretion. In contrast, both low and high concentrations of xylosides altered HS and CS composition. RNAseq of treated cells demonstrated alterations in gene expression only after treatment with millimolar concentration of xylosides that had no effect on cell morphology. These observations support a novel action of xylosides on neuronal cells. Public Library of Science 2022-06-28 /pmc/articles/PMC9239447/ /pubmed/35763520 http://dx.doi.org/10.1371/journal.pone.0269972 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Mencio, Caitlin P.
Tilve, Sharada M.
Suzuki, Masato
Higashi, Kohei
Katagiri, Yasuhiro
Geller, Herbert M.
A novel cytoskeletal action of xylosides
title A novel cytoskeletal action of xylosides
title_full A novel cytoskeletal action of xylosides
title_fullStr A novel cytoskeletal action of xylosides
title_full_unstemmed A novel cytoskeletal action of xylosides
title_short A novel cytoskeletal action of xylosides
title_sort novel cytoskeletal action of xylosides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239447/
https://www.ncbi.nlm.nih.gov/pubmed/35763520
http://dx.doi.org/10.1371/journal.pone.0269972
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