Cargando…

Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation

The primary cilium is a hair-like immotile organelle with specific membrane receptors, including the receptor of Hedgehog signaling, smoothened. The cilium organized in preosteoblasts promotes differentiation of the cells into osteoblasts (osteoblast differentiation) by mediating Hedgehog signaling...

Descripción completa

Detalles Bibliográficos
Autores principales: Saito, Masaki, Hirano, Marina, Izumi, Tomohiro, Mori, Yu, Ito, Kentaro, Saitoh, Yurika, Terada, Nobuo, Sato, Takeya, Sukegawa, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878336/
https://www.ncbi.nlm.nih.gov/pubmed/35216233
http://dx.doi.org/10.3390/ijms23042094
_version_ 1784658637127417856
author Saito, Masaki
Hirano, Marina
Izumi, Tomohiro
Mori, Yu
Ito, Kentaro
Saitoh, Yurika
Terada, Nobuo
Sato, Takeya
Sukegawa, Jun
author_facet Saito, Masaki
Hirano, Marina
Izumi, Tomohiro
Mori, Yu
Ito, Kentaro
Saitoh, Yurika
Terada, Nobuo
Sato, Takeya
Sukegawa, Jun
author_sort Saito, Masaki
collection PubMed
description The primary cilium is a hair-like immotile organelle with specific membrane receptors, including the receptor of Hedgehog signaling, smoothened. The cilium organized in preosteoblasts promotes differentiation of the cells into osteoblasts (osteoblast differentiation) by mediating Hedgehog signaling to achieve bone formation. Notably, 4.1G is a plasma membrane-associated cytoskeletal protein that plays essential roles in various tissues, including the peripheral nervous system, testis, and retina. However, its function in the bone remains unexplored. In this study, we identified 4.1G expression in the bone. We found that, in the 4.1G-knockout mice, calcium deposits and primary cilium formation were suppressed in the trabecular bone, which is preosteoblast-rich region of the newborn tibia, indicating that 4.1G is a prerequisite for osteoblast differentiation by organizing the primary cilia in preosteoblasts. Next, we found that the primary cilium was elongated in the differentiating mouse preosteoblast cell line MC3T3-E1, whereas the knockdown of 4.1G suppressed its elongation. Moreover, 4.1G-knockdown suppressed the induction of the cilia-mediated Hedgehog signaling and subsequent osteoblast differentiation. These results demonstrate a new regulatory mechanism of 4.1G in bone formation that promotes the primary ciliogenesis in the differentiating preosteoblasts and induction of cilia-mediated osteoblast differentiation, resulting in bone formation at the newborn stage.
format Online
Article
Text
id pubmed-8878336
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-88783362022-02-26 Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation Saito, Masaki Hirano, Marina Izumi, Tomohiro Mori, Yu Ito, Kentaro Saitoh, Yurika Terada, Nobuo Sato, Takeya Sukegawa, Jun Int J Mol Sci Article The primary cilium is a hair-like immotile organelle with specific membrane receptors, including the receptor of Hedgehog signaling, smoothened. The cilium organized in preosteoblasts promotes differentiation of the cells into osteoblasts (osteoblast differentiation) by mediating Hedgehog signaling to achieve bone formation. Notably, 4.1G is a plasma membrane-associated cytoskeletal protein that plays essential roles in various tissues, including the peripheral nervous system, testis, and retina. However, its function in the bone remains unexplored. In this study, we identified 4.1G expression in the bone. We found that, in the 4.1G-knockout mice, calcium deposits and primary cilium formation were suppressed in the trabecular bone, which is preosteoblast-rich region of the newborn tibia, indicating that 4.1G is a prerequisite for osteoblast differentiation by organizing the primary cilia in preosteoblasts. Next, we found that the primary cilium was elongated in the differentiating mouse preosteoblast cell line MC3T3-E1, whereas the knockdown of 4.1G suppressed its elongation. Moreover, 4.1G-knockdown suppressed the induction of the cilia-mediated Hedgehog signaling and subsequent osteoblast differentiation. These results demonstrate a new regulatory mechanism of 4.1G in bone formation that promotes the primary ciliogenesis in the differentiating preosteoblasts and induction of cilia-mediated osteoblast differentiation, resulting in bone formation at the newborn stage. MDPI 2022-02-14 /pmc/articles/PMC8878336/ /pubmed/35216233 http://dx.doi.org/10.3390/ijms23042094 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Saito, Masaki
Hirano, Marina
Izumi, Tomohiro
Mori, Yu
Ito, Kentaro
Saitoh, Yurika
Terada, Nobuo
Sato, Takeya
Sukegawa, Jun
Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title_full Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title_fullStr Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title_full_unstemmed Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title_short Cytoskeletal Protein 4.1G Is Essential for the Primary Ciliogenesis and Osteoblast Differentiation in Bone Formation
title_sort cytoskeletal protein 4.1g is essential for the primary ciliogenesis and osteoblast differentiation in bone formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878336/
https://www.ncbi.nlm.nih.gov/pubmed/35216233
http://dx.doi.org/10.3390/ijms23042094
work_keys_str_mv AT saitomasaki cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT hiranomarina cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT izumitomohiro cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT moriyu cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT itokentaro cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT saitohyurika cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT teradanobuo cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT satotakeya cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation
AT sukegawajun cytoskeletalprotein41gisessentialfortheprimaryciliogenesisandosteoblastdifferentiationinboneformation