College of Life Science and Graduate School of Biotechnology, Kyung Hee University, Seochon-dong, Kiheung-go, Yongin-si, Geonggi-do 17104, Korea .
Department of Medical Engineering, Graduate School, Kyung Hee University, Seoul 02447, Korea.
Int J Mol Sci. 2020 Dec 30;22(1):325. doi: 10.3390/ijms22010325.
Near the bone remodeling compartments (BRC), extracellular calcium concentration (Ca) 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). 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.
在骨改建部位(BRC)附近,细胞外钙浓度(Ca)局部升高,靠近 BRC 的骨髓基质细胞(BMSCs)可能会暴露在高钙浓度下。钙敏感受体(CaSR)通过感知细胞外钙(Ca)水平的波动,在维持细胞外钙稳态方面发挥着关键作用。当人骨髓基质细胞(hBMSCs)暴露于不同的钙浓度(1.8、3、5、10、30mM)时,中高细胞外钙浓度(3-5mM)刺激增殖,而高钙浓度(30mM)抑制增殖。暴露于不同的钙浓度不会诱导细胞凋亡分数的显著差异。多系分化潜能评估显示,除了高钙浓度(30mM)处理组外,各钙浓度组之间没有显著差异,高钙浓度处理组在体外成骨分化后导致钙化增加。钙敏感受体抑制剂 NPS2143 的处理消除了对 hBMSCs 增殖和迁移的刺激作用,表明 CaSR 参与其中。这些结果表明,BRC 附近的钙浓度梯度可能通过钙敏感受体作为成骨细胞-破骨细胞偶联机制在骨改建中发挥重要作用。