中国康复理论与实践
中國康複理論與實踐
중국강복이론여실천
CHINESE JOURNAL OF REHABILITATION THEORY & PRACTICE
2014年
4期
322-326
,共5页
宋国丽%周翠红%张宇%张小云
宋國麗%週翠紅%張宇%張小雲
송국려%주취홍%장우%장소운
静磁场%骨髓间充质干细胞%增殖%骨向分化%大鼠
靜磁場%骨髓間充質榦細胞%增殖%骨嚮分化%大鼠
정자장%골수간충질간세포%증식%골향분화%대서
static magnetic field%mesenchymal stem cells%proliferation%osteogenic differentiation%rats
目的:研究0.25 T、0.35 T、0.42 T静磁场持续或间歇曝磁对骨髓间充质干细胞(MSCs)增殖及骨向分化的影响。方法全骨髓贴壁筛选法分离MSCs,取第三代MSCs采用强度分别为0.25 T、0.35 T、0.42 T静磁场持续曝磁或间歇曝磁,CCK-8法检测各组细胞增殖活力,并观察0.35 T连续曝磁后MSCs碱性磷酸酶活性、骨钙素含量。结果细胞经过磁场处理后,与对照组相比,细胞增殖活力均降低,连续曝磁第7天效果最为显著(P<0.001),而0.25 T、0.35 T间歇曝磁第2~8天持续表现出显著抑制效应(P<0.001)。0.35 T持续曝磁后,MSCs碱性磷酸酶活性和骨钙素水平均增高(P<0.05)。结论0.25 T、0.35 T、0.42 T静磁场连续曝磁或间歇曝磁均可抑制MSCs增殖,0.35 T连续曝磁能促进MSCs向成骨细胞方向分化。
目的:研究0.25 T、0.35 T、0.42 T靜磁場持續或間歇曝磁對骨髓間充質榦細胞(MSCs)增殖及骨嚮分化的影響。方法全骨髓貼壁篩選法分離MSCs,取第三代MSCs採用彊度分彆為0.25 T、0.35 T、0.42 T靜磁場持續曝磁或間歇曝磁,CCK-8法檢測各組細胞增殖活力,併觀察0.35 T連續曝磁後MSCs堿性燐痠酶活性、骨鈣素含量。結果細胞經過磁場處理後,與對照組相比,細胞增殖活力均降低,連續曝磁第7天效果最為顯著(P<0.001),而0.25 T、0.35 T間歇曝磁第2~8天持續錶現齣顯著抑製效應(P<0.001)。0.35 T持續曝磁後,MSCs堿性燐痠酶活性和骨鈣素水平均增高(P<0.05)。結論0.25 T、0.35 T、0.42 T靜磁場連續曝磁或間歇曝磁均可抑製MSCs增殖,0.35 T連續曝磁能促進MSCs嚮成骨細胞方嚮分化。
목적:연구0.25 T、0.35 T、0.42 T정자장지속혹간헐폭자대골수간충질간세포(MSCs)증식급골향분화적영향。방법전골수첩벽사선법분리MSCs,취제삼대MSCs채용강도분별위0.25 T、0.35 T、0.42 T정자장지속폭자혹간헐폭자,CCK-8법검측각조세포증식활력,병관찰0.35 T련속폭자후MSCs감성린산매활성、골개소함량。결과세포경과자장처리후,여대조조상비,세포증식활력균강저,련속폭자제7천효과최위현저(P<0.001),이0.25 T、0.35 T간헐폭자제2~8천지속표현출현저억제효응(P<0.001)。0.35 T지속폭자후,MSCs감성린산매활성화골개소수평균증고(P<0.05)。결론0.25 T、0.35 T、0.42 T정자장련속폭자혹간헐폭자균가억제MSCs증식,0.35 T련속폭자능촉진MSCs향성골세포방향분화。
Objective To investigate the effect of exposure to 0.25 T, 0.35 T, 0.42 T static magnetic fields (SMF) on the proliferation and osteogenic differentiation of mesenchymal stem cells (MSCs). Methods Primary bone marrow MSCs were obtained from Sprague-Dawley rats and screened by adhesive method. MSCs were exposed to 0.25 T, 0.35 T, 0.42 T SMF continuously and 24 h intermittently respectively. The cell proliferation activity was detected by Cell Counting Kit (CCK-8) assay. The osteogenic differentiation markers including alkaline phosphatase (ALP) activity and osteocalcin were analyzed after continuously exposure to 0.35 T SMF. Results Compared with the control group, the proliferation activity of SMF-treated cells significantly decreased, especially on the 7th day (P<0.001) after continuous exposure, and on the 2nd to 8th day in 0.25 T, 0.35 T SMF intermittent exposure groups (P<0.001). Both the alkaline phosphatase activity and the lev-el of osteocalcin significantly increased in MSCs after continuous exposure to 0.35 T SMF (P<0.05). Conclusion Continuous or intermittent exposure to 0.25 T, 0.35 T and 0.42 T SMF could effectively inhibit the proliferation of MSCs. Continuous exposure to 0.35 T SMF could enhance the osteogenic differentiation of MSCs.