The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts

Osteoclasts are bone resorbing cells that participate in the maintenance of bone health. Pathological increase in osteoclast activity causes bone loss, eventually resulting in osteoporosis. Actin cytoskeleton of osteoclasts organizes into a belt of podosomes, which sustains the bone resorption appar...

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Autores principales: Justine Maurin, Anne Morel, David Guérit, Julien Cau, Serge Urbach, Anne Blangy, Guillaume Bompard
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:0a9f88f193f6499097d2d7155cc4004e2021-11-18T09:52:13ZThe Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts2296-634X10.3389/fcell.2021.778887https://doaj.org/article/0a9f88f193f6499097d2d7155cc4004e2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.778887/fullhttps://doaj.org/toc/2296-634XOsteoclasts are bone resorbing cells that participate in the maintenance of bone health. Pathological increase in osteoclast activity causes bone loss, eventually resulting in osteoporosis. Actin cytoskeleton of osteoclasts organizes into a belt of podosomes, which sustains the bone resorption apparatus and is maintained by microtubules. Better understanding of the molecular mechanisms regulating osteoclast cytoskeleton is key to understand the mechanisms of bone resorption, in particular to propose new strategies against osteoporosis. We reported recently that β-tubulin isotype TUBB6 is key for cytoskeleton organization in osteoclasts and for bone resorption. Here, using an osteoclast model CRISPR/Cas9 KO for Tubb6, we show that TUBB6 controls both microtubule and actin dynamics in osteoclasts. Osteoclasts KO for Tubb6 have reduced microtubule growth speed with longer growth life time, higher levels of acetylation, and smaller EB1-caps. On the other hand, lack of TUBB6 increases podosome life time while the belt of podosomes is destabilized. Finally, we performed proteomic analyses of osteoclast microtubule-associated protein enriched fractions. This highlighted ARHGAP10 as a new microtubule-associated protein, which binding to microtubules appears to be negatively regulated by TUBB6. ARHGAP10 is a negative regulator of CDC42 activity, which participates in actin organization in osteoclasts. Our results suggest that TUBB6 plays a key role in the control of microtubule and actin cytoskeleton dynamics in osteoclasts. Moreover, by controlling ARHGAP10 association with microtubules, TUBB6 may participate in the local control of CDC42 activity to ensure efficient bone resorption.Justine MaurinAnne MorelDavid GuéritJulien CauSerge UrbachAnne BlangyGuillaume BompardFrontiers Media S.A.articleosteoclasttubulin isotypemicrotubuleactinbone resorptionGRAF2Biology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic osteoclast
tubulin isotype
microtubule
actin
bone resorption
GRAF2
Biology (General)
QH301-705.5
spellingShingle osteoclast
tubulin isotype
microtubule
actin
bone resorption
GRAF2
Biology (General)
QH301-705.5
Justine Maurin
Anne Morel
David Guérit
Julien Cau
Serge Urbach
Anne Blangy
Guillaume Bompard
The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
description Osteoclasts are bone resorbing cells that participate in the maintenance of bone health. Pathological increase in osteoclast activity causes bone loss, eventually resulting in osteoporosis. Actin cytoskeleton of osteoclasts organizes into a belt of podosomes, which sustains the bone resorption apparatus and is maintained by microtubules. Better understanding of the molecular mechanisms regulating osteoclast cytoskeleton is key to understand the mechanisms of bone resorption, in particular to propose new strategies against osteoporosis. We reported recently that β-tubulin isotype TUBB6 is key for cytoskeleton organization in osteoclasts and for bone resorption. Here, using an osteoclast model CRISPR/Cas9 KO for Tubb6, we show that TUBB6 controls both microtubule and actin dynamics in osteoclasts. Osteoclasts KO for Tubb6 have reduced microtubule growth speed with longer growth life time, higher levels of acetylation, and smaller EB1-caps. On the other hand, lack of TUBB6 increases podosome life time while the belt of podosomes is destabilized. Finally, we performed proteomic analyses of osteoclast microtubule-associated protein enriched fractions. This highlighted ARHGAP10 as a new microtubule-associated protein, which binding to microtubules appears to be negatively regulated by TUBB6. ARHGAP10 is a negative regulator of CDC42 activity, which participates in actin organization in osteoclasts. Our results suggest that TUBB6 plays a key role in the control of microtubule and actin cytoskeleton dynamics in osteoclasts. Moreover, by controlling ARHGAP10 association with microtubules, TUBB6 may participate in the local control of CDC42 activity to ensure efficient bone resorption.
format article
author Justine Maurin
Anne Morel
David Guérit
Julien Cau
Serge Urbach
Anne Blangy
Guillaume Bompard
author_facet Justine Maurin
Anne Morel
David Guérit
Julien Cau
Serge Urbach
Anne Blangy
Guillaume Bompard
author_sort Justine Maurin
title The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
title_short The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
title_full The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
title_fullStr The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
title_full_unstemmed The Beta-Tubulin Isotype TUBB6 Controls Microtubule and Actin Dynamics in Osteoclasts
title_sort beta-tubulin isotype tubb6 controls microtubule and actin dynamics in osteoclasts
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/0a9f88f193f6499097d2d7155cc4004e
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