CAJ | 학술논문

目的：探讨雷奈酸锶（ Sr）对高浓度地塞米松（ Dex）作用下大鼠成骨细胞（ OB）的影响。方法采用大鼠骨髓基质干细胞（ BMSCs）来源的成骨细胞，运用MTT试剂盒和AKP试剂盒分别测定Sr对细胞增殖和分化的影响，定量PCR方法测定Sr对高浓度地塞米松作用下成骨钙素（ OC）和转化生长因子－β（ TGF－β）表达的影响。结果 Sr浓度在10－5、10－4 mol／L时，能够促进OB增殖和分化（P＜0．01）；Sr浓度为10－4mmol／L能够有效拮抗高浓度Dex（10－5 mol／L）对成骨细胞分化抑制作用（P＜0．01），并能逆转Dex对成骨相关基因OC和TGF－β的抑制作用（P＜0．05，P＜0．01）。结论 Sr能够对大鼠BMSCs来源的成骨细胞的增殖、分化有促进作用，同时10－4 mol／L Sr可以拮抗Dex（10－5 mol／L）对ALP和成骨相关基因的抑制作用。为Sr防治糖皮质激素性骨质疏松提供了细胞学依据。
목적：탐토뢰내산송（ Sr）대고농도지새미송（ Dex）작용하대서성골세포（ OB）적영향。방법채용대서골수기질간세포（ BMSCs）래원적성골세포，운용MTT시제합화AKP시제합분별측정Sr대세포증식화분화적영향，정량PCR방법측정Sr대고농도지새미송작용하성골개소（ OC）화전화생장인자－β（ TGF－β）표체적영향。결과 Sr농도재10－5、10－4 mol／L시，능구촉진OB증식화분화（P＜0．01）；Sr농도위10－4mmol／L능구유효길항고농도Dex（10－5 mol／L）대성골세포분화억제작용（P＜0．01），병능역전Dex대성골상관기인OC화TGF－β적억제작용（P＜0．05，P＜0．01）。결론 Sr능구대대서BMSCs래원적성골세포적증식、분화유촉진작용，동시10－4 mol／L Sr가이길항Dex（10－5 mol／L）대ALP화성골상관기인적억제작용。위Sr방치당피질격소성골질소송제공료세포학의거。
Objective To study the effect of strontium ranelate ( Sr ) on rat osteoblasts under high dexamethasone ( Dex ) concentration.Methods Using rat bone marrow stromal stem cell-derived osteoblasts, the effect of Sr on the proliferation and differentiation of osteoblasts was detected with MTT and AKP commercial kits.The expression of OC and TGF-βunder high Dex concentration was detected with RT-PCR.Results Proliferation and differentiation of OB were stimulated at concentrations of 10 -5 mol/L and 10 -4 mol/L of Sr ( P<0.01 ) .Sr at concentration of 10 -4 mol/L effectively antagonized the inhibitory effect of Dex on osteoblast differentiation (P<0.01), and reverted the inhibitory effect of Dex on OC and TGF-β(P<0.05, P<0.01). Conclusion Sr can promote the proliferation and differentiation of OB derived from BMSCs.Sr at concentration of 10 -4 mol/L can effectively antagonize the inhibitory effect of Dex (10 -5 mol/L) on ALP, OC, and TGF-β.It provide the cytological evidence for prevention and treatment of GIOP with Sr.