TY - JOUR
T1 - Coupling of angiogenesis and odontogenesis orchestrates tooth mineralization in mice
AU - Matsubara, Tomoko
AU - Iga, Takahito
AU - Sugiura, Yuki
AU - Kusumoto, Dai
AU - Sanosaka, Tsukasa
AU - Tai-Nagara, Ikue
AU - Takeda, Norihiko
AU - Fong, Guo Hua
AU - Ito, Kosei
AU - Ema, Masatsugu
AU - Okano, Hideyuki
AU - Kohyama, Jun
AU - Suematsu, Makoto
AU - Kubota, Yoshiaki
N1 - Funding Information:
This work was supported by Grants-in-Aid for Specially Promoted Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (18H05042, 18K19553, and 19H03397); by Japan Agency for Medical Research and Development–PRIME (AMED-PRIME; JP20gm6210017h0002 and 21gm6210017h0003); by Japan Science and Technology Agency (MoonshotR&D; JPMJMS 2024); and by research grants from the following: Inamori Foundation, Kao Foundation for Arts and Culture, Takeda Science Foundation, Mochida Memorial Foundation, Mitsubishi Foundation, Cell Science Research Foundation, SENSHIN Medical Research Foundation, Sumitomo Foundation, Daiichi Sankyo Foundation of Life Science, Naito Foundation, Uehara Memorial Foundation, and Toray Science Foundation.
Publisher Copyright:
© 2022 Matsubara et al.
PY - 2022/4/4
Y1 - 2022/4/4
N2 - 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.
AB - 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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U2 - 10.1084/jem.20211789
DO - 10.1084/jem.20211789
M3 - Article
C2 - 35319724
AN - SCOPUS:85126863405
SN - 0022-1007
VL - 219
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 4
M1 - e20211789
ER -