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High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice

STUDY DESIGN. Basic experiments in a mouse model of ossification of the posterior longitudinal ligament (OPLL). OBJECTIVE. To assess the osteogenic potential of mesenchymal stem cells (MSCs) obtained from muscle and adipose tissue in Tiptoe-walking (ttw) mice, in which cervical OPLL compresses the s...

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Autores principales: Liu, Xizhe, Kumagai, Gentaro, Wada, Kanichiro, Tanaka, Toshihiro, Asari, Toru, Oishi, Kazuki, Fujita, Taku, Mizukami, Hiroki, Furukawa, Ken-Ichi, Ishibashi, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704663/
https://www.ncbi.nlm.nih.gov/pubmed/28632647
http://dx.doi.org/10.1097/BRS.0000000000002266
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author Liu, Xizhe
Kumagai, Gentaro
Wada, Kanichiro
Tanaka, Toshihiro
Asari, Toru
Oishi, Kazuki
Fujita, Taku
Mizukami, Hiroki
Furukawa, Ken-Ichi
Ishibashi, Yasuyuki
author_facet Liu, Xizhe
Kumagai, Gentaro
Wada, Kanichiro
Tanaka, Toshihiro
Asari, Toru
Oishi, Kazuki
Fujita, Taku
Mizukami, Hiroki
Furukawa, Ken-Ichi
Ishibashi, Yasuyuki
author_sort Liu, Xizhe
collection PubMed
description STUDY DESIGN. Basic experiments in a mouse model of ossification of the posterior longitudinal ligament (OPLL). OBJECTIVE. To assess the osteogenic potential of mesenchymal stem cells (MSCs) obtained from muscle and adipose tissue in Tiptoe-walking (ttw) mice, in which cervical OPLL compresses the spinal cord and causes motor and sensory dysfunction. SUMMARY OF BACKGROUND DATA. In humans, MSCs have been implicated in the pathogenesis of cervical OPLL. Cervical OPLL in ttw mice causes chronic compression of the spinal cord. Few studies have compared the MSC osteogenic potential with behavioral changes in an OPLL animal model. METHODS. We compared the osteogenic potential and behavioral characteristics of MSCs from ttw mice (4 to 20 weeks old) with those from control wild-type mice (without hyperostosis). Ligament ossification was monitored by micro-computed tomography and pathology; tissues were double stained with fluorescent antibodies against markers for MSCs (CD45 and CD105), at 8 weeks. The Basso Mouse Scale was used to assess motor function, and heat and mechanical tests to assess sensory function. The osteogenic potential of adipose and muscle MSCs was assessed by Alizarin Red S absorbance, staining for osteogenic mineralization, and real-time quantitative polymerase chain reaction for osteogenesis-related genes. RESULTS. Spinal-ligament ossification began in ttw mice at 8 weeks of age, and the ossified area increased with age. Immunofluorescence staining identified MSCs in the ossification area. The ttw mice became hyposensitive at 8 weeks of age, and Basso Mouse Scale scores showed motor-function deficits starting at 12 weeks of age. Alizarin Red S staining for mineralization showed a higher osteogenic potential in the adipose- and muscle-derived MSCs from ttw mice than from wild-type mice at 4, 8, and 20 weeks of age. Real-time quantitative polymerase chain reaction showed that ttw MSCs strongly expressed osteogenesis-related genes. CONCLUSION. MSCs derived from muscle and adipose tissue in ttw mice had a high osteogenic potential. Level of Evidence: N/A
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spelling pubmed-57046632017-12-11 High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice Liu, Xizhe Kumagai, Gentaro Wada, Kanichiro Tanaka, Toshihiro Asari, Toru Oishi, Kazuki Fujita, Taku Mizukami, Hiroki Furukawa, Ken-Ichi Ishibashi, Yasuyuki Spine (Phila Pa 1976) Basic Science STUDY DESIGN. Basic experiments in a mouse model of ossification of the posterior longitudinal ligament (OPLL). OBJECTIVE. To assess the osteogenic potential of mesenchymal stem cells (MSCs) obtained from muscle and adipose tissue in Tiptoe-walking (ttw) mice, in which cervical OPLL compresses the spinal cord and causes motor and sensory dysfunction. SUMMARY OF BACKGROUND DATA. In humans, MSCs have been implicated in the pathogenesis of cervical OPLL. Cervical OPLL in ttw mice causes chronic compression of the spinal cord. Few studies have compared the MSC osteogenic potential with behavioral changes in an OPLL animal model. METHODS. We compared the osteogenic potential and behavioral characteristics of MSCs from ttw mice (4 to 20 weeks old) with those from control wild-type mice (without hyperostosis). Ligament ossification was monitored by micro-computed tomography and pathology; tissues were double stained with fluorescent antibodies against markers for MSCs (CD45 and CD105), at 8 weeks. The Basso Mouse Scale was used to assess motor function, and heat and mechanical tests to assess sensory function. The osteogenic potential of adipose and muscle MSCs was assessed by Alizarin Red S absorbance, staining for osteogenic mineralization, and real-time quantitative polymerase chain reaction for osteogenesis-related genes. RESULTS. Spinal-ligament ossification began in ttw mice at 8 weeks of age, and the ossified area increased with age. Immunofluorescence staining identified MSCs in the ossification area. The ttw mice became hyposensitive at 8 weeks of age, and Basso Mouse Scale scores showed motor-function deficits starting at 12 weeks of age. Alizarin Red S staining for mineralization showed a higher osteogenic potential in the adipose- and muscle-derived MSCs from ttw mice than from wild-type mice at 4, 8, and 20 weeks of age. Real-time quantitative polymerase chain reaction showed that ttw MSCs strongly expressed osteogenesis-related genes. CONCLUSION. MSCs derived from muscle and adipose tissue in ttw mice had a high osteogenic potential. Level of Evidence: N/A Lippincott Williams & Wilkins 2017-12-01 2017-06-19 /pmc/articles/PMC5704663/ /pubmed/28632647 http://dx.doi.org/10.1097/BRS.0000000000002266 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Basic Science
Liu, Xizhe
Kumagai, Gentaro
Wada, Kanichiro
Tanaka, Toshihiro
Asari, Toru
Oishi, Kazuki
Fujita, Taku
Mizukami, Hiroki
Furukawa, Ken-Ichi
Ishibashi, Yasuyuki
High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title_full High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title_fullStr High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title_full_unstemmed High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title_short High Osteogenic Potential of Adipose- and Muscle-derived Mesenchymal Stem Cells in Spinal-Ossification Model Mice
title_sort high osteogenic potential of adipose- and muscle-derived mesenchymal stem cells in spinal-ossification model mice
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704663/
https://www.ncbi.nlm.nih.gov/pubmed/28632647
http://dx.doi.org/10.1097/BRS.0000000000002266
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