Abed E, Moreau R
Laboratoire du Métabolisme Osseux, Centre BioMed, Département des Sciences Biologiques, Université du Québec à Montréal, Montréal, Québec, Canada.
Cell Prolif. 2007 Dec;40(6):849-65. doi: 10.1111/j.1365-2184.2007.00476.x.
Bone tissue in the adult is continuously being remodelled, and overall bone mass is maintained constant by the balance between osteoclastic bone resorption and osteoblastic bone formation. Adequate osteoblastic proliferation is essential for both appropriate formation and for regulation of resorption, and thereby the maintenance of bone remodelling equilibrium.
Here, we have investigated the roles of melastatin-like transient receptor potential 6 and 7 (TRPM6, TRPM7), which are calcium (Ca2+) and magnesium (Mg2+) conducting channels, during proliferation of human osteoblasts.
Genetic expression of TRPM6 and TRPM7 was shown in human osteoblast-like MG-63, SaOS and U2-OS cells, and reduction of extracellular Mg2+ or Ca2+ led to a decrease of cell proliferation. Concomitant reduction of both ions further accentuated reduction of cell proliferation. Expression of TRPM7 channels was increased under conditions of reduced extracellular Mg2+ and Ca2+ levels whereas expression of TRPM6 was not modified, suggesting compensatory mechanisms afforded by TRPM7 in order to maintain intracellular ion homeostasis. Pre-incubation of cells in reduced extracellular Mg2+ conditions led to activation of Ca2+ and Mg2+ influx. Reduction of TRPM7 expression by specific siRNA prevented latter influx and inhibited cell proliferation.
Our results indicate that extracellular Mg2+ and Ca2+ deficiency reduces the proliferation of human osteoblastic cells. Expression and activity of TRPM7 is modulated by extracellular Mg2+ and Ca2+ availability, indicating that TRPM7 channels are involved in intracellular ion homeostasis and proliferation of osteoblasts.
成人体内的骨组织不断重塑,破骨细胞的骨吸收与成骨细胞的骨形成之间的平衡维持着整体骨量的恒定。充足的成骨细胞增殖对于适当的骨形成和骨吸收调节以及维持骨重塑平衡至关重要。
在此,我们研究了褪黑素样瞬时受体电位6和7(TRPM6、TRPM7),即钙(Ca2+)和镁(Mg2+)传导通道,在人成骨细胞增殖过程中的作用。
TRPM6和TRPM7的基因表达在人成骨样MG-63、SaOS和U2-OS细胞中被检测到,细胞外Mg2+或Ca2+的减少导致细胞增殖下降。两种离子同时减少进一步加剧了细胞增殖的降低。在细胞外Mg2+和Ca2+水平降低的条件下,TRPM7通道的表达增加,而TRPM6的表达未改变,这表明TRPM7提供了补偿机制以维持细胞内离子稳态。在细胞外Mg2+减少的条件下对细胞进行预孵育导致Ca2+和Mg2+内流激活。通过特异性小干扰RNA降低TRPM7的表达可阻止后者的内流并抑制细胞增殖。
我们的结果表明,细胞外Mg2+和Ca2+缺乏会降低人成骨细胞的增殖。TRPM7的表达和活性受细胞外Mg2+和Ca2+可用性的调节,表明TRPM7通道参与成骨细胞的细胞内离子稳态和增殖。