Elevated extracellular calcium ions promote proliferation and migration of mesenchymal stem cells via increasing osteopontin expression
Autor: | Amir Roshanzadeh, Sin-Hye Oh, Ju Han Song, Eung-Sam Kim, Hee-Su Hwang, Jung-Woo Kim, Jeong-Tae Koh, Mi Nam Lee |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Male Clinical Biochemistry lcsh:Medicine Calvaria Biochemistry Bone resorption Article Bone remodeling lcsh:Biochemistry 03 medical and health sciences Mice 0302 clinical medicine Cell Movement Cell Line Tumor Extracellular medicine Animals lcsh:QD415-436 Osteopontin Bone regeneration Molecular Biology Cells Cultured Cell Proliferation biology Chemistry lcsh:R Mesenchymal stem cell Mesenchymal Stem Cells Cell biology Mice Inbred C57BL 030104 developmental biology medicine.anatomical_structure 030220 oncology & carcinogenesis biology.protein Molecular Medicine Calcium Homeostasis |
Zdroj: | Experimental & Molecular Medicine Experimental and Molecular Medicine, Vol 50, Iss 11, Pp 1-16 (2018) |
ISSN: | 2092-6413 1226-3613 |
Popis: | Supplementation of mesenchymal stem cells (MSCs) at sites of bone resorption is required for bone homeostasis because of the non-proliferation and short lifespan properties of the osteoblasts. Calcium ions (Ca2+) are released from the bone surfaces during osteoclast-mediated bone resorption. However, how elevated extracellular Ca2+ concentrations would alter MSCs behavior in the proximal sites of bone resorption is largely unknown. In this study, we investigated the effect of extracellular Ca2+ on MSCs phenotype depending on Ca2+ concentrations. We found that the elevated extracellular Ca2+ promoted cell proliferation and matrix mineralization of MSCs. In addition, MSCs induced the expression and secretion of osteopontin (OPN), which enhanced MSCs migration under the elevated extracellular Ca2+ conditions. We developed in vitro osteoclast-mediated bone resorption conditions using mouse calvaria bone slices and demonstrated Ca2+ is released from bone resorption surfaces. We also showed that the MSCs phenotype, including cell proliferation and migration, changed when the cells were treated with a bone resorption-conditioned medium. These findings suggest that the dynamic changes in Ca2+ concentrations in the microenvironments of bone remodeling surfaces modulate MSCs phenotype and thereby contribute to bone regeneration. Bone formation: released calcium could stimulate stem cells Studies with mouse cells and bone samples indicate how calcium ions released during the normal turnover of bone promote the supplementation of stem cells needed to make new bone during routine “remodeling” and regeneration after injury. Our bones are degraded and remodeled continuously, requiring the controlled supplement of stem cells that create bone-forming cells called osteoblasts. Jeong-Tae Koh and colleagues at Chonnam National University, Gwangju, South Korea, exposed the relevant stem cells to increased concentrations of external calcium ions. This promoted cell proliferation and migration that allow the cells to support new bone formation. The research suggests this effect on stem cells may be achieved by calcium ions released directly from bone as it is naturally degraded. The findings may help researchers develop new ways to encourage bone regeneration after injury and surgery. |
Databáze: | OpenAIRE |
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