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Dynamics of the sealing zone in cultured osteoclasts

Bone resorption by osteoclasts (OCs) depends on the formation and stability of the sealing zone (SZ), a peripheral belt of actin and integrin‐based podosomes. Recent studies demonstrated that the SZ is a highly dynamic structure, undergoing cycles of assembly and disassembly. In this study, we explo...

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Autores principales: Batsir, Sarit, Geiger, Benjamin, Kam, Zvi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347972/
https://www.ncbi.nlm.nih.gov/pubmed/27997747
http://dx.doi.org/10.1002/cm.21350
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author Batsir, Sarit
Geiger, Benjamin
Kam, Zvi
author_facet Batsir, Sarit
Geiger, Benjamin
Kam, Zvi
author_sort Batsir, Sarit
collection PubMed
description Bone resorption by osteoclasts (OCs) depends on the formation and stability of the sealing zone (SZ), a peripheral belt of actin and integrin‐based podosomes. Recent studies demonstrated that the SZ is a highly dynamic structure, undergoing cycles of assembly and disassembly. In this study, we explored the mechanisms underlying the regulation of SZ stability and reorganization in OCs cultured on glass slides, and forming an SZ‐like podosome belt (SZL). By monitoring this belt in cultured RAW264.7 cells expressing GFP‐tagged actin, we show here that SZL stability is usually locally regulated, and its dissociation, occurring mostly in concave segments, is manifested in the loss of both podosome coherence, and actin belt continuity. Double labeling of cells for actin and tubulin indicated that microtubules (MTs) are mostly confined by the inner aspect of the stable SZL‐associated actin belt. However, in unstable regions of the SZL, MTs tend to extend radially, across the SZL, toward the cell edge. Disruption of MTs by nocodazole induces SZ disassembly, without affecting individual podosome stability. Inspection of the MT network indicates that it is enriched along stable SZL regions, while bypassing disorganized regions. These results suggest that the SZL is stabilized by MTs flanking its inner aspect, while disruption or misalignment of MTs leads to SZL destabilization. We further demonstrate that the MT‐associated protein dynamin2 is involved in the regulation of SZL stability, and dynamin2 knockdown or inactivation cause SZL destabilization.
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spelling pubmed-53479722017-03-23 Dynamics of the sealing zone in cultured osteoclasts Batsir, Sarit Geiger, Benjamin Kam, Zvi Cytoskeleton (Hoboken) Research Articles Bone resorption by osteoclasts (OCs) depends on the formation and stability of the sealing zone (SZ), a peripheral belt of actin and integrin‐based podosomes. Recent studies demonstrated that the SZ is a highly dynamic structure, undergoing cycles of assembly and disassembly. In this study, we explored the mechanisms underlying the regulation of SZ stability and reorganization in OCs cultured on glass slides, and forming an SZ‐like podosome belt (SZL). By monitoring this belt in cultured RAW264.7 cells expressing GFP‐tagged actin, we show here that SZL stability is usually locally regulated, and its dissociation, occurring mostly in concave segments, is manifested in the loss of both podosome coherence, and actin belt continuity. Double labeling of cells for actin and tubulin indicated that microtubules (MTs) are mostly confined by the inner aspect of the stable SZL‐associated actin belt. However, in unstable regions of the SZL, MTs tend to extend radially, across the SZL, toward the cell edge. Disruption of MTs by nocodazole induces SZ disassembly, without affecting individual podosome stability. Inspection of the MT network indicates that it is enriched along stable SZL regions, while bypassing disorganized regions. These results suggest that the SZL is stabilized by MTs flanking its inner aspect, while disruption or misalignment of MTs leads to SZL destabilization. We further demonstrate that the MT‐associated protein dynamin2 is involved in the regulation of SZL stability, and dynamin2 knockdown or inactivation cause SZL destabilization. John Wiley and Sons Inc. 2017-02-08 2017-02 /pmc/articles/PMC5347972/ /pubmed/27997747 http://dx.doi.org/10.1002/cm.21350 Text en © 2017 The Authors Cytoskeleton Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Batsir, Sarit
Geiger, Benjamin
Kam, Zvi
Dynamics of the sealing zone in cultured osteoclasts
title Dynamics of the sealing zone in cultured osteoclasts
title_full Dynamics of the sealing zone in cultured osteoclasts
title_fullStr Dynamics of the sealing zone in cultured osteoclasts
title_full_unstemmed Dynamics of the sealing zone in cultured osteoclasts
title_short Dynamics of the sealing zone in cultured osteoclasts
title_sort dynamics of the sealing zone in cultured osteoclasts
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347972/
https://www.ncbi.nlm.nih.gov/pubmed/27997747
http://dx.doi.org/10.1002/cm.21350
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