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A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration

The redevelopment/regeneration pattern of amputated limbs from a blastema in salamander suggests that enhanced regeneration might be achieved by mimicking the developmental microenvironment. Inspired by the discovery that the expression of magnesium transporter‐1 (MagT1), a selective magnesium (Mg)...

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Autores principales: Lin, Sihan, Yang, Guangzheng, Jiang, Fei, Zhou, Mingliang, Yin, Shi, Tang, Yanmei, Tang, Tingting, Zhang, Zhiyuan, Zhang, Wenjie, Jiang, Xinquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662069/
https://www.ncbi.nlm.nih.gov/pubmed/31380166
http://dx.doi.org/10.1002/advs.201900209
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author Lin, Sihan
Yang, Guangzheng
Jiang, Fei
Zhou, Mingliang
Yin, Shi
Tang, Yanmei
Tang, Tingting
Zhang, Zhiyuan
Zhang, Wenjie
Jiang, Xinquan
author_facet Lin, Sihan
Yang, Guangzheng
Jiang, Fei
Zhou, Mingliang
Yin, Shi
Tang, Yanmei
Tang, Tingting
Zhang, Zhiyuan
Zhang, Wenjie
Jiang, Xinquan
author_sort Lin, Sihan
collection PubMed
description The redevelopment/regeneration pattern of amputated limbs from a blastema in salamander suggests that enhanced regeneration might be achieved by mimicking the developmental microenvironment. Inspired by the discovery that the expression of magnesium transporter‐1 (MagT1), a selective magnesium (Mg) transporter, is significantly upregulated in the endochondral ossification region of mouse embryos, a Mg‐enriched 3D culture system is proposed to provide an embryonic‐like environment for stem cells. First, the optimum concentration of Mg ions (Mg(2+)) for creating the osteogenic microenvironment is screened by evaluating MagT1 expression levels, which correspond to the osteogenic differentiation capacity of stem cells. The results reveal that Mg(2+) selectively activates the mitogen‐activated protein kinase/extracellular regulated kinase (MAPK/ERK) pathway to stimulate osteogenic differentiation, and Mg(2+) influx via MagT1 is profoundly involved in this process. Then, Mg‐enriched microspheres are fabricated at the appropriate size to ensure the viability of the encapsulated cells. A series of experiments show that the Mg‐enriched microenvironment not only stimulates the osteogenic differentiation of stem cells but also promotes neovascularization. Obvious vascularized bone regeneration is achieved in vivo using these Mg‐enriched cell delivery vehicles. The findings suggest that biomaterials mimicking the developmental microenvironment might be promising tools to enhance tissue regeneration.
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spelling pubmed-66620692019-08-02 A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration Lin, Sihan Yang, Guangzheng Jiang, Fei Zhou, Mingliang Yin, Shi Tang, Yanmei Tang, Tingting Zhang, Zhiyuan Zhang, Wenjie Jiang, Xinquan Adv Sci (Weinh) Full Papers The redevelopment/regeneration pattern of amputated limbs from a blastema in salamander suggests that enhanced regeneration might be achieved by mimicking the developmental microenvironment. Inspired by the discovery that the expression of magnesium transporter‐1 (MagT1), a selective magnesium (Mg) transporter, is significantly upregulated in the endochondral ossification region of mouse embryos, a Mg‐enriched 3D culture system is proposed to provide an embryonic‐like environment for stem cells. First, the optimum concentration of Mg ions (Mg(2+)) for creating the osteogenic microenvironment is screened by evaluating MagT1 expression levels, which correspond to the osteogenic differentiation capacity of stem cells. The results reveal that Mg(2+) selectively activates the mitogen‐activated protein kinase/extracellular regulated kinase (MAPK/ERK) pathway to stimulate osteogenic differentiation, and Mg(2+) influx via MagT1 is profoundly involved in this process. Then, Mg‐enriched microspheres are fabricated at the appropriate size to ensure the viability of the encapsulated cells. A series of experiments show that the Mg‐enriched microenvironment not only stimulates the osteogenic differentiation of stem cells but also promotes neovascularization. Obvious vascularized bone regeneration is achieved in vivo using these Mg‐enriched cell delivery vehicles. The findings suggest that biomaterials mimicking the developmental microenvironment might be promising tools to enhance tissue regeneration. John Wiley and Sons Inc. 2019-04-18 /pmc/articles/PMC6662069/ /pubmed/31380166 http://dx.doi.org/10.1002/advs.201900209 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Lin, Sihan
Yang, Guangzheng
Jiang, Fei
Zhou, Mingliang
Yin, Shi
Tang, Yanmei
Tang, Tingting
Zhang, Zhiyuan
Zhang, Wenjie
Jiang, Xinquan
A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title_full A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title_fullStr A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title_full_unstemmed A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title_short A Magnesium‐Enriched 3D Culture System that Mimics the Bone Development Microenvironment for Vascularized Bone Regeneration
title_sort magnesium‐enriched 3d culture system that mimics the bone development microenvironment for vascularized bone regeneration
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662069/
https://www.ncbi.nlm.nih.gov/pubmed/31380166
http://dx.doi.org/10.1002/advs.201900209
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