Cargando…

Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets

Aggrecan, a chondroitin sulfate (CS) proteoglycan, forms lattice-like extracellular matrix structures called perineuronal nets (PNNs). Neocortical PNNs primarily ensheath parvalbumin-expressing inhibitory neurons (parvalbumin, PV cells) late in brain development. Emerging evidence indicates that PNN...

Descripción completa

Detalles Bibliográficos
Autores principales: Miyata, Shinji, Nadanaka, Satomi, Igarashi, Michihiro, Kitagawa, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801575/
https://www.ncbi.nlm.nih.gov/pubmed/29456495
http://dx.doi.org/10.3389/fnint.2018.00003
_version_ 1783298370881716224
author Miyata, Shinji
Nadanaka, Satomi
Igarashi, Michihiro
Kitagawa, Hiroshi
author_facet Miyata, Shinji
Nadanaka, Satomi
Igarashi, Michihiro
Kitagawa, Hiroshi
author_sort Miyata, Shinji
collection PubMed
description Aggrecan, a chondroitin sulfate (CS) proteoglycan, forms lattice-like extracellular matrix structures called perineuronal nets (PNNs). Neocortical PNNs primarily ensheath parvalbumin-expressing inhibitory neurons (parvalbumin, PV cells) late in brain development. Emerging evidence indicates that PNNs promote the maturation of PV cells by enhancing the incorporation of homeobox protein Otx2 and regulating experience-dependent neural plasticity. Wisteria floribunda agglutinin (WFA), an N-acetylgalactosamine-specific plant lectin, binds to the CS chains of aggrecan and has been widely used to visualize PNNs. Although PNNs show substantial molecular heterogeneity, the importance of this heterogeneity in neural plasticity remains unknown. Here, in addition to WFA lectin, we used the two monoclonal antibodies Cat315 and Cat316, both of which recognize the glycan structures of aggrecan, to investigate the molecular heterogeneity of PNNs. WFA detected the highest number of PNNs in all cortical layers, whereas Cat315 and Cat316 labeled only a subset of PNNs. WFA(+), Cat315(+), and Cat316(+) PNNs showed different laminar distributions in the adult visual cortex. WFA, Cat315 and Cat316 detected distinct, but partially overlapping, populations of PNNs. Based on the reactivities of these probes, we categorized PNNs into four groups. We found that two subpopulation of PNNs, one with higher and one with lower WFA-staining are differentially labeled by Cat316 and Cat315, respectively. CS chains recognized by Cat316 were diminished in mice deficient in an enzyme involved in the initiation of CS-biosynthesis. Furthermore, WFA(+) and Cat316(+) aggrecan were spatially segregated and formed microdomains in a single PNN. Otx2 co-localized with Cat316(+) but not with WFA(+) aggrecan in PNNs. Our results suggest that the heterogeneity of PNNs around PV cells may affect the functional maturation of these cells.
format Online
Article
Text
id pubmed-5801575
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-58015752018-02-16 Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets Miyata, Shinji Nadanaka, Satomi Igarashi, Michihiro Kitagawa, Hiroshi Front Integr Neurosci Neuroscience Aggrecan, a chondroitin sulfate (CS) proteoglycan, forms lattice-like extracellular matrix structures called perineuronal nets (PNNs). Neocortical PNNs primarily ensheath parvalbumin-expressing inhibitory neurons (parvalbumin, PV cells) late in brain development. Emerging evidence indicates that PNNs promote the maturation of PV cells by enhancing the incorporation of homeobox protein Otx2 and regulating experience-dependent neural plasticity. Wisteria floribunda agglutinin (WFA), an N-acetylgalactosamine-specific plant lectin, binds to the CS chains of aggrecan and has been widely used to visualize PNNs. Although PNNs show substantial molecular heterogeneity, the importance of this heterogeneity in neural plasticity remains unknown. Here, in addition to WFA lectin, we used the two monoclonal antibodies Cat315 and Cat316, both of which recognize the glycan structures of aggrecan, to investigate the molecular heterogeneity of PNNs. WFA detected the highest number of PNNs in all cortical layers, whereas Cat315 and Cat316 labeled only a subset of PNNs. WFA(+), Cat315(+), and Cat316(+) PNNs showed different laminar distributions in the adult visual cortex. WFA, Cat315 and Cat316 detected distinct, but partially overlapping, populations of PNNs. Based on the reactivities of these probes, we categorized PNNs into four groups. We found that two subpopulation of PNNs, one with higher and one with lower WFA-staining are differentially labeled by Cat316 and Cat315, respectively. CS chains recognized by Cat316 were diminished in mice deficient in an enzyme involved in the initiation of CS-biosynthesis. Furthermore, WFA(+) and Cat316(+) aggrecan were spatially segregated and formed microdomains in a single PNN. Otx2 co-localized with Cat316(+) but not with WFA(+) aggrecan in PNNs. Our results suggest that the heterogeneity of PNNs around PV cells may affect the functional maturation of these cells. Frontiers Media S.A. 2018-02-02 /pmc/articles/PMC5801575/ /pubmed/29456495 http://dx.doi.org/10.3389/fnint.2018.00003 Text en Copyright © 2018 Miyata, Nadanaka, Igarashi and Kitagawa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Miyata, Shinji
Nadanaka, Satomi
Igarashi, Michihiro
Kitagawa, Hiroshi
Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title_full Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title_fullStr Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title_full_unstemmed Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title_short Structural Variation of Chondroitin Sulfate Chains Contributes to the Molecular Heterogeneity of Perineuronal Nets
title_sort structural variation of chondroitin sulfate chains contributes to the molecular heterogeneity of perineuronal nets
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801575/
https://www.ncbi.nlm.nih.gov/pubmed/29456495
http://dx.doi.org/10.3389/fnint.2018.00003
work_keys_str_mv AT miyatashinji structuralvariationofchondroitinsulfatechainscontributestothemolecularheterogeneityofperineuronalnets
AT nadanakasatomi structuralvariationofchondroitinsulfatechainscontributestothemolecularheterogeneityofperineuronalnets
AT igarashimichihiro structuralvariationofchondroitinsulfatechainscontributestothemolecularheterogeneityofperineuronalnets
AT kitagawahiroshi structuralvariationofchondroitinsulfatechainscontributestothemolecularheterogeneityofperineuronalnets