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CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment
Near the bone remodeling compartments (BRC), extracellular calcium concentration (Ca(2+)(o)) is locally elevated and bone marrow stromal cells (BMSCs) close to the BRC can be exposed to high calcium concentration. The calcium-sensing receptor (CaSR) is known to play a key role in maintaining extrace...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795180/ https://www.ncbi.nlm.nih.gov/pubmed/33396907 http://dx.doi.org/10.3390/ijms22010325 |
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author | Cho, Hyunji Lee, Jisoo Jang, Seoyoung Lee, Jungsun Oh, Tong In Son, Youngsook Lee, EunAh |
author_facet | Cho, Hyunji Lee, Jisoo Jang, Seoyoung Lee, Jungsun Oh, Tong In Son, Youngsook Lee, EunAh |
author_sort | Cho, Hyunji |
collection | PubMed |
description | Near the bone remodeling compartments (BRC), extracellular calcium concentration (Ca(2+)(o)) is locally elevated and bone marrow stromal cells (BMSCs) close to the BRC can be exposed to high calcium concentration. The calcium-sensing receptor (CaSR) is known to play a key role in maintaining extracellular calcium homeostasis by sensing fluctuations in the levels of extracellular calcium (Ca(2+)(o)). When human BMSCs (hBMSCs) were exposed to various calcium concentrations (1.8, 3, 5, 10, 30 mM), moderate-high extracellular calcium concentrations (3–5 mM) stimulated proliferation, while a high calcium concentration (30 mM) inhibited the proliferation. Exposure to various calcium concentrations did not induce significant differences in the apoptotic cell fraction. Evaluation of multi-lineage differentiation potential showed no significant difference among various calcium concentration groups, except for the high calcium concentration (30 mM) treated group, which resulted in increased calcification after in vitro osteogenic differentiation. Treatment of NPS2143, a CaSR inhibitor, abolished the stimulatory effect on hBMSCs proliferation and migration indicating that CaSR is involved. These results suggest that the calcium concentration gradient near the BRC may play an important role in bone remodeling by acting as an osteoblast–osteoclast coupling mechanism through CaSR. |
format | Online Article Text |
id | pubmed-7795180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77951802021-01-10 CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment Cho, Hyunji Lee, Jisoo Jang, Seoyoung Lee, Jungsun Oh, Tong In Son, Youngsook Lee, EunAh Int J Mol Sci Article Near the bone remodeling compartments (BRC), extracellular calcium concentration (Ca(2+)(o)) is locally elevated and bone marrow stromal cells (BMSCs) close to the BRC can be exposed to high calcium concentration. The calcium-sensing receptor (CaSR) is known to play a key role in maintaining extracellular calcium homeostasis by sensing fluctuations in the levels of extracellular calcium (Ca(2+)(o)). When human BMSCs (hBMSCs) were exposed to various calcium concentrations (1.8, 3, 5, 10, 30 mM), moderate-high extracellular calcium concentrations (3–5 mM) stimulated proliferation, while a high calcium concentration (30 mM) inhibited the proliferation. Exposure to various calcium concentrations did not induce significant differences in the apoptotic cell fraction. Evaluation of multi-lineage differentiation potential showed no significant difference among various calcium concentration groups, except for the high calcium concentration (30 mM) treated group, which resulted in increased calcification after in vitro osteogenic differentiation. Treatment of NPS2143, a CaSR inhibitor, abolished the stimulatory effect on hBMSCs proliferation and migration indicating that CaSR is involved. These results suggest that the calcium concentration gradient near the BRC may play an important role in bone remodeling by acting as an osteoblast–osteoclast coupling mechanism through CaSR. MDPI 2020-12-30 /pmc/articles/PMC7795180/ /pubmed/33396907 http://dx.doi.org/10.3390/ijms22010325 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cho, Hyunji Lee, Jisoo Jang, Seoyoung Lee, Jungsun Oh, Tong In Son, Youngsook Lee, EunAh CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title | CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title_full | CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title_fullStr | CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title_full_unstemmed | CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title_short | CaSR-Mediated hBMSCs Activity Modulation: Additional Coupling Mechanism in Bone Remodeling Compartment |
title_sort | casr-mediated hbmscs activity modulation: additional coupling mechanism in bone remodeling compartment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795180/ https://www.ncbi.nlm.nih.gov/pubmed/33396907 http://dx.doi.org/10.3390/ijms22010325 |
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