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Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development

Bone marrow development and endochondral bone formation occur simultaneously. During endochondral ossification, periosteal vasculatures and stromal progenitors invade the primary avascular cartilaginous anlage, which induces primitive marrow development. We previously determined that bone marrow pod...

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Autores principales: Tamura, Shogo, Mukaide, Masato, Katsuragi, Yumi, Fujii, Wataru, Odaira, Koya, Suzuki, Nobuaki, Tsukiji, Nagaharu, Okamoto, Shuichi, Suzuki, Atsuo, Kanematsu, Takeshi, Katsumi, Akira, Takagi, Akira, Ikeda, Katsuhide, Ueyama, Jun, Hirayama, Masaaki, Suzuki-Inoue, Katsue, Matsushita, Tadashi, Kojima, Tetsuhito, Hayakawa, Fumihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019254/
https://www.ncbi.nlm.nih.gov/pubmed/35304101
http://dx.doi.org/10.1016/j.jbc.2022.101833
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author Tamura, Shogo
Mukaide, Masato
Katsuragi, Yumi
Fujii, Wataru
Odaira, Koya
Suzuki, Nobuaki
Tsukiji, Nagaharu
Okamoto, Shuichi
Suzuki, Atsuo
Kanematsu, Takeshi
Katsumi, Akira
Takagi, Akira
Ikeda, Katsuhide
Ueyama, Jun
Hirayama, Masaaki
Suzuki-Inoue, Katsue
Matsushita, Tadashi
Kojima, Tetsuhito
Hayakawa, Fumihiko
author_facet Tamura, Shogo
Mukaide, Masato
Katsuragi, Yumi
Fujii, Wataru
Odaira, Koya
Suzuki, Nobuaki
Tsukiji, Nagaharu
Okamoto, Shuichi
Suzuki, Atsuo
Kanematsu, Takeshi
Katsumi, Akira
Takagi, Akira
Ikeda, Katsuhide
Ueyama, Jun
Hirayama, Masaaki
Suzuki-Inoue, Katsue
Matsushita, Tadashi
Kojima, Tetsuhito
Hayakawa, Fumihiko
author_sort Tamura, Shogo
collection PubMed
description Bone marrow development and endochondral bone formation occur simultaneously. During endochondral ossification, periosteal vasculatures and stromal progenitors invade the primary avascular cartilaginous anlage, which induces primitive marrow development. We previously determined that bone marrow podoplanin (PDPN)-expressing stromal cells exist in the perivascular microenvironment and promote megakaryopoiesis and erythropoiesis. In this study, we aimed to examine the involvement of PDPN-expressing stromal cells in postnatal bone marrow generation. Using histological analysis, we observed that periosteum-derived PDPN-expressing stromal cells infiltrated the cartilaginous anlage of the postnatal epiphysis and populated on the primitive vasculature of secondary ossification center. Furthermore, immunophenotyping and cellular characteristic analyses indicated that the PDPN-expressing stromal cells constituted a subpopulation of the skeletal stem cell lineage. In vitro xenovascular model cocultured with human umbilical vein endothelial cells and PDPN-expressing skeletal stem cell progenies showed that PDPN-expressing stromal cells maintained vascular integrity via the release of angiogenic factors and vascular basement membrane-related extracellular matrices. We show that in this process, Notch signal activation committed the PDPN-expressing stromal cells into a dominant state with basement membrane-related extracellular matrices, especially type IV collagens. Our findings suggest that the PDPN-expressing stromal cells regulate the integrity of the primitive vasculatures in the epiphyseal nascent marrow. To the best of our knowledge, this is the first study to comprehensively examine how PDPN-expressing stromal cells contribute to marrow development and homeostasis.
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spelling pubmed-90192542022-04-22 Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development Tamura, Shogo Mukaide, Masato Katsuragi, Yumi Fujii, Wataru Odaira, Koya Suzuki, Nobuaki Tsukiji, Nagaharu Okamoto, Shuichi Suzuki, Atsuo Kanematsu, Takeshi Katsumi, Akira Takagi, Akira Ikeda, Katsuhide Ueyama, Jun Hirayama, Masaaki Suzuki-Inoue, Katsue Matsushita, Tadashi Kojima, Tetsuhito Hayakawa, Fumihiko J Biol Chem Research Article Bone marrow development and endochondral bone formation occur simultaneously. During endochondral ossification, periosteal vasculatures and stromal progenitors invade the primary avascular cartilaginous anlage, which induces primitive marrow development. We previously determined that bone marrow podoplanin (PDPN)-expressing stromal cells exist in the perivascular microenvironment and promote megakaryopoiesis and erythropoiesis. In this study, we aimed to examine the involvement of PDPN-expressing stromal cells in postnatal bone marrow generation. Using histological analysis, we observed that periosteum-derived PDPN-expressing stromal cells infiltrated the cartilaginous anlage of the postnatal epiphysis and populated on the primitive vasculature of secondary ossification center. Furthermore, immunophenotyping and cellular characteristic analyses indicated that the PDPN-expressing stromal cells constituted a subpopulation of the skeletal stem cell lineage. In vitro xenovascular model cocultured with human umbilical vein endothelial cells and PDPN-expressing skeletal stem cell progenies showed that PDPN-expressing stromal cells maintained vascular integrity via the release of angiogenic factors and vascular basement membrane-related extracellular matrices. We show that in this process, Notch signal activation committed the PDPN-expressing stromal cells into a dominant state with basement membrane-related extracellular matrices, especially type IV collagens. Our findings suggest that the PDPN-expressing stromal cells regulate the integrity of the primitive vasculatures in the epiphyseal nascent marrow. To the best of our knowledge, this is the first study to comprehensively examine how PDPN-expressing stromal cells contribute to marrow development and homeostasis. American Society for Biochemistry and Molecular Biology 2022-03-15 /pmc/articles/PMC9019254/ /pubmed/35304101 http://dx.doi.org/10.1016/j.jbc.2022.101833 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Tamura, Shogo
Mukaide, Masato
Katsuragi, Yumi
Fujii, Wataru
Odaira, Koya
Suzuki, Nobuaki
Tsukiji, Nagaharu
Okamoto, Shuichi
Suzuki, Atsuo
Kanematsu, Takeshi
Katsumi, Akira
Takagi, Akira
Ikeda, Katsuhide
Ueyama, Jun
Hirayama, Masaaki
Suzuki-Inoue, Katsue
Matsushita, Tadashi
Kojima, Tetsuhito
Hayakawa, Fumihiko
Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title_full Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title_fullStr Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title_full_unstemmed Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title_short Periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
title_sort periosteum-derived podoplanin-expressing stromal cells regulate nascent vascularization during epiphyseal marrow development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019254/
https://www.ncbi.nlm.nih.gov/pubmed/35304101
http://dx.doi.org/10.1016/j.jbc.2022.101833
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