Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.

BACKGROUND: Heparan sulfate proteoglycans (HSPGs) are one of the basic constituents of plasma membranes. Specific molecular interactions between HSPGs and a number of extracellular ligands have been reported. Mechanisms involved in controlling the localization and abundance of HSPG on specific domai...

Full description

Bibliographic Details
Main Authors: Katarzyna A Podyma-Inoue, Miki Hara-Yokoyama, Tamayuki Shinomura, Tomoko Kimura, Masaki Yanagishita
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3291576?pdf=render
_version_ 1828186225084727296
author Katarzyna A Podyma-Inoue
Miki Hara-Yokoyama
Tamayuki Shinomura
Tomoko Kimura
Masaki Yanagishita
author_facet Katarzyna A Podyma-Inoue
Miki Hara-Yokoyama
Tamayuki Shinomura
Tomoko Kimura
Masaki Yanagishita
author_sort Katarzyna A Podyma-Inoue
collection DOAJ
description BACKGROUND: Heparan sulfate proteoglycans (HSPGs) are one of the basic constituents of plasma membranes. Specific molecular interactions between HSPGs and a number of extracellular ligands have been reported. Mechanisms involved in controlling the localization and abundance of HSPG on specific domains on the cell surface, such as membrane rafts, could play important regulatory roles in signal transduction. METHODOLOGY/PRINCIPAL FINDINGS: Using metabolic radiolabeling and sucrose-density gradient ultracentrifugation techniques, we identified [(35)S]sulfate-labeled macromolecules associated with detergent-resistant membranes (DRMs) isolated from a rat parathyroid cell line. DRM fractions showed high specific radioactivity ([(35)S]sulfate/mg protein), implying the specific recruitment of HSPGs to the membrane rafts. Identity of DRM-associated [(35)S]sulfate-labeled molecules as HSPGs was confirmed by Western blotting with antibodies that recognize heparan sulfate (HS)-derived epitope. Analyses of core proteins by SDS-PAGE revealed bands with an apparent MW of syndecan-4 (30-33 kDa) and syndecan-1 (70 kDa) suggesting the presence of rafts with various HSPG species. DRM fractions enriched with HSPGs were characterized by high sphingomyelin content and found to only partially overlap with the fractions enriched in ganglioside GM1. HSPGs could be also detected in DRMs even after prior treatment of cells with heparitinase. CONCLUSIONS/SIGNIFICANCE: Both syndecan-1 and syndecan-4 have been found to specifically associate with membrane rafts and their association seemed independent of intact HS chains. Membrane rafts in which HSPGs reside were also enriched with sphingomyelin, suggesting their possible involvement in FGF signaling. Further studies, involving proteomic characterization of membrane domains containing HSPGs might improve our knowledge on the nature of HSPG-ligand interactions and their role in different signaling platforms.
first_indexed 2024-04-12T07:16:37Z
format Article
id doaj.art-eee2d64d02734219af6627139495d288
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-12T07:16:37Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-eee2d64d02734219af6627139495d2882022-12-22T03:42:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3235110.1371/journal.pone.0032351Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.Katarzyna A Podyma-InoueMiki Hara-YokoyamaTamayuki ShinomuraTomoko KimuraMasaki YanagishitaBACKGROUND: Heparan sulfate proteoglycans (HSPGs) are one of the basic constituents of plasma membranes. Specific molecular interactions between HSPGs and a number of extracellular ligands have been reported. Mechanisms involved in controlling the localization and abundance of HSPG on specific domains on the cell surface, such as membrane rafts, could play important regulatory roles in signal transduction. METHODOLOGY/PRINCIPAL FINDINGS: Using metabolic radiolabeling and sucrose-density gradient ultracentrifugation techniques, we identified [(35)S]sulfate-labeled macromolecules associated with detergent-resistant membranes (DRMs) isolated from a rat parathyroid cell line. DRM fractions showed high specific radioactivity ([(35)S]sulfate/mg protein), implying the specific recruitment of HSPGs to the membrane rafts. Identity of DRM-associated [(35)S]sulfate-labeled molecules as HSPGs was confirmed by Western blotting with antibodies that recognize heparan sulfate (HS)-derived epitope. Analyses of core proteins by SDS-PAGE revealed bands with an apparent MW of syndecan-4 (30-33 kDa) and syndecan-1 (70 kDa) suggesting the presence of rafts with various HSPG species. DRM fractions enriched with HSPGs were characterized by high sphingomyelin content and found to only partially overlap with the fractions enriched in ganglioside GM1. HSPGs could be also detected in DRMs even after prior treatment of cells with heparitinase. CONCLUSIONS/SIGNIFICANCE: Both syndecan-1 and syndecan-4 have been found to specifically associate with membrane rafts and their association seemed independent of intact HS chains. Membrane rafts in which HSPGs reside were also enriched with sphingomyelin, suggesting their possible involvement in FGF signaling. Further studies, involving proteomic characterization of membrane domains containing HSPGs might improve our knowledge on the nature of HSPG-ligand interactions and their role in different signaling platforms.http://europepmc.org/articles/PMC3291576?pdf=render
spellingShingle Katarzyna A Podyma-Inoue
Miki Hara-Yokoyama
Tamayuki Shinomura
Tomoko Kimura
Masaki Yanagishita
Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
PLoS ONE
title Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
title_full Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
title_fullStr Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
title_full_unstemmed Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
title_short Syndecans reside in sphingomyelin-enriched low-density fractions of the plasma membrane isolated from a parathyroid cell line.
title_sort syndecans reside in sphingomyelin enriched low density fractions of the plasma membrane isolated from a parathyroid cell line
url http://europepmc.org/articles/PMC3291576?pdf=render
work_keys_str_mv AT katarzynaapodymainoue syndecansresideinsphingomyelinenrichedlowdensityfractionsoftheplasmamembraneisolatedfromaparathyroidcellline
AT mikiharayokoyama syndecansresideinsphingomyelinenrichedlowdensityfractionsoftheplasmamembraneisolatedfromaparathyroidcellline
AT tamayukishinomura syndecansresideinsphingomyelinenrichedlowdensityfractionsoftheplasmamembraneisolatedfromaparathyroidcellline
AT tomokokimura syndecansresideinsphingomyelinenrichedlowdensityfractionsoftheplasmamembraneisolatedfromaparathyroidcellline
AT masakiyanagishita syndecansresideinsphingomyelinenrichedlowdensityfractionsoftheplasmamembraneisolatedfromaparathyroidcellline