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Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice

The skeletal system consists of bones and teeth, both of which are hardened via mineralization to support daily physical activity and mastication. The precise mechanism for this process, especially how blood vessels contribute to tissue mineralization, remains incompletely understood. Here, we estab...

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Autores principales: Matsubara, Tomoko, Iga, Takahito, Sugiura, Yuki, Kusumoto, Dai, Sanosaka, Tsukasa, Tai-Nagara, Ikue, Takeda, Norihiko, Fong, Guo-Hua, Ito, Kosei, Ema, Masatsugu, Okano, Hideyuki, Kohyama, Jun, Suematsu, Makoto, Kubota, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952600/
https://www.ncbi.nlm.nih.gov/pubmed/35319724
http://dx.doi.org/10.1084/jem.20211789
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author Matsubara, Tomoko
Iga, Takahito
Sugiura, Yuki
Kusumoto, Dai
Sanosaka, Tsukasa
Tai-Nagara, Ikue
Takeda, Norihiko
Fong, Guo-Hua
Ito, Kosei
Ema, Masatsugu
Okano, Hideyuki
Kohyama, Jun
Suematsu, Makoto
Kubota, Yoshiaki
author_facet Matsubara, Tomoko
Iga, Takahito
Sugiura, Yuki
Kusumoto, Dai
Sanosaka, Tsukasa
Tai-Nagara, Ikue
Takeda, Norihiko
Fong, Guo-Hua
Ito, Kosei
Ema, Masatsugu
Okano, Hideyuki
Kohyama, Jun
Suematsu, Makoto
Kubota, Yoshiaki
author_sort Matsubara, Tomoko
collection PubMed
description The skeletal system consists of bones and teeth, both of which are hardened via mineralization to support daily physical activity and mastication. The precise mechanism for this process, especially how blood vessels contribute to tissue mineralization, remains incompletely understood. Here, we established an imaging technique to visualize the 3D structure of the tooth vasculature at a single-cell level. Using this technique combined with single-cell RNA sequencing, we identified a unique endothelial subtype specialized to dentinogenesis, a process of tooth mineralization, termed periodontal tip-like endothelial cells. These capillaries exhibit high angiogenic activity and plasticity under the control of odontoblasts; in turn, the capillaries trigger odontoblast maturation. Metabolomic analysis demonstrated that the capillaries perform the phosphate delivery required for dentinogenesis. Taken together, our data identified the fundamental cell-to-cell communications that orchestrate tooth formation, angiogenic–odontogenic coupling, a distinct mechanism compared to the angiogenic–osteogenic coupling in bones. This mechanism contributes to our understanding concerning the functional diversity of organotypic vasculature.
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spelling pubmed-89526002022-10-04 Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice Matsubara, Tomoko Iga, Takahito Sugiura, Yuki Kusumoto, Dai Sanosaka, Tsukasa Tai-Nagara, Ikue Takeda, Norihiko Fong, Guo-Hua Ito, Kosei Ema, Masatsugu Okano, Hideyuki Kohyama, Jun Suematsu, Makoto Kubota, Yoshiaki J Exp Med Article The skeletal system consists of bones and teeth, both of which are hardened via mineralization to support daily physical activity and mastication. The precise mechanism for this process, especially how blood vessels contribute to tissue mineralization, remains incompletely understood. Here, we established an imaging technique to visualize the 3D structure of the tooth vasculature at a single-cell level. Using this technique combined with single-cell RNA sequencing, we identified a unique endothelial subtype specialized to dentinogenesis, a process of tooth mineralization, termed periodontal tip-like endothelial cells. These capillaries exhibit high angiogenic activity and plasticity under the control of odontoblasts; in turn, the capillaries trigger odontoblast maturation. Metabolomic analysis demonstrated that the capillaries perform the phosphate delivery required for dentinogenesis. Taken together, our data identified the fundamental cell-to-cell communications that orchestrate tooth formation, angiogenic–odontogenic coupling, a distinct mechanism compared to the angiogenic–osteogenic coupling in bones. This mechanism contributes to our understanding concerning the functional diversity of organotypic vasculature. Rockefeller University Press 2022-03-23 /pmc/articles/PMC8952600/ /pubmed/35319724 http://dx.doi.org/10.1084/jem.20211789 Text en © 2022 Matsubara et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Matsubara, Tomoko
Iga, Takahito
Sugiura, Yuki
Kusumoto, Dai
Sanosaka, Tsukasa
Tai-Nagara, Ikue
Takeda, Norihiko
Fong, Guo-Hua
Ito, Kosei
Ema, Masatsugu
Okano, Hideyuki
Kohyama, Jun
Suematsu, Makoto
Kubota, Yoshiaki
Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title_full Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title_fullStr Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title_full_unstemmed Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title_short Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
title_sort coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8952600/
https://www.ncbi.nlm.nih.gov/pubmed/35319724
http://dx.doi.org/10.1084/jem.20211789
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