中华航空航天医学杂志
中華航空航天醫學雜誌
중화항공항천의학잡지
CHINESE JOURNAL OF AEROSPACE MEDICINE
2011年
2期
97-101,封2
,共6页
王脉桃%黄震%杨力%陈宏%苏嘉霖%麦燕兴%杨锐%周焕成
王脈桃%黃震%楊力%陳宏%囌嘉霖%麥燕興%楊銳%週煥成
왕맥도%황진%양력%진굉%소가림%맥연흥%양예%주환성
失重模拟%成骨细胞%细胞骨架%碱性磷酸酶%骨钙素
失重模擬%成骨細胞%細胞骨架%堿性燐痠酶%骨鈣素
실중모의%성골세포%세포골가%감성린산매%골개소
Weightlessness simulation%Osteoblast%Cytoskeleton%Alkaline
目的 研究模拟微重力诱导小鼠成骨细胞微丝结构改变对碱性磷酸酶(alkaline phosphatase,ALP)及骨钙蛋白(osteocalcin,OCN)的影响,探讨失重导致骨质疏松的机制.方法本研究以已建株的小鼠成骨样细胞株(MC3T3-E1)作为对象,以回转器模拟微重力效应.实验将细胞分为4组:模拟微重力组、0.5 μg/ml细胞松弛素B组、模拟微重力+0.5 μg/ml细胞松弛素B组及正常重力组(对照组).培养48 h后,利用异硫氰酸荧光素鬼笔环肽(fluoresceine isothiocyanate phalloidin,FITC-phalloidin)进行免疫荧光染色,在激光共聚焦显微镜下观察各组细胞微丝的变化;同时用ALP试剂检测各组细胞培养液内ALP的酶活性,采用ELISA法检测各组细胞裂解液中OCN的表达量.结果 除正常重力组外,其余各组细胞微丝结构都出现了不同程度的解聚,张力纤维减少,失去方向性,以模拟微重力+0.5 μg/ml细胞松弛素B组改变最为明显.和正常重力组比较,其余各组ALP的酶活性和OCN的表达量均成下降趋势(F=17.23、121.91,P<0.01),且模拟微重力+0.5 μg/ml细胞松弛素B组与模拟微重力组和0.5 μg/ml细胞松弛素B组这两组之间的差别都有统计学意义(P<0.05).结论 微重力影响成骨细胞ALP的酶活性及OCN的表达可能与微重力诱导细胞骨架微丝解聚相关.
目的 研究模擬微重力誘導小鼠成骨細胞微絲結構改變對堿性燐痠酶(alkaline phosphatase,ALP)及骨鈣蛋白(osteocalcin,OCN)的影響,探討失重導緻骨質疏鬆的機製.方法本研究以已建株的小鼠成骨樣細胞株(MC3T3-E1)作為對象,以迴轉器模擬微重力效應.實驗將細胞分為4組:模擬微重力組、0.5 μg/ml細胞鬆弛素B組、模擬微重力+0.5 μg/ml細胞鬆弛素B組及正常重力組(對照組).培養48 h後,利用異硫氰痠熒光素鬼筆環肽(fluoresceine isothiocyanate phalloidin,FITC-phalloidin)進行免疫熒光染色,在激光共聚焦顯微鏡下觀察各組細胞微絲的變化;同時用ALP試劑檢測各組細胞培養液內ALP的酶活性,採用ELISA法檢測各組細胞裂解液中OCN的錶達量.結果 除正常重力組外,其餘各組細胞微絲結構都齣現瞭不同程度的解聚,張力纖維減少,失去方嚮性,以模擬微重力+0.5 μg/ml細胞鬆弛素B組改變最為明顯.和正常重力組比較,其餘各組ALP的酶活性和OCN的錶達量均成下降趨勢(F=17.23、121.91,P<0.01),且模擬微重力+0.5 μg/ml細胞鬆弛素B組與模擬微重力組和0.5 μg/ml細胞鬆弛素B組這兩組之間的差彆都有統計學意義(P<0.05).結論 微重力影響成骨細胞ALP的酶活性及OCN的錶達可能與微重力誘導細胞骨架微絲解聚相關.
목적 연구모의미중력유도소서성골세포미사결구개변대감성린산매(alkaline phosphatase,ALP)급골개단백(osteocalcin,OCN)적영향,탐토실중도치골질소송적궤제.방법본연구이이건주적소서성골양세포주(MC3T3-E1)작위대상,이회전기모의미중력효응.실험장세포분위4조:모의미중력조、0.5 μg/ml세포송이소B조、모의미중력+0.5 μg/ml세포송이소B조급정상중력조(대조조).배양48 h후,이용이류청산형광소귀필배태(fluoresceine isothiocyanate phalloidin,FITC-phalloidin)진행면역형광염색,재격광공취초현미경하관찰각조세포미사적변화;동시용ALP시제검측각조세포배양액내ALP적매활성,채용ELISA법검측각조세포렬해액중OCN적표체량.결과 제정상중력조외,기여각조세포미사결구도출현료불동정도적해취,장력섬유감소,실거방향성,이모의미중력+0.5 μg/ml세포송이소B조개변최위명현.화정상중력조비교,기여각조ALP적매활성화OCN적표체량균성하강추세(F=17.23、121.91,P<0.01),차모의미중력+0.5 μg/ml세포송이소B조여모의미중력조화0.5 μg/ml세포송이소B조저량조지간적차별도유통계학의의(P<0.05).결론 미중력영향성골세포ALP적매활성급OCN적표체가능여미중력유도세포골가미사해취상관.
Objective To research the effects of the mouse's microfilament cytoskeleton change induced by simulated microgravity on alkaline phosphatase (ALP) and osteocalcin (OCN), and then to explore the mechanism of weightlessness leading osteoporosis. Methods Research object was the osteoblast-like cell line of mouse (MC3T3-E1). Microgravity was simulated by rotary cell culture system. Cells were divided into four groups: simulated microgravity group, 0.5 μg/ml cytochalasin B group, simulated microgravity+0.5 μg/ml cytochalasin B group and normal gravity group. Cells had been cultivated for 48 h when immunofluorescence staining was made by fluoresceine isothiocyanate phalloidin (FITC-phallacidin). Then the changes of cell microfilament were observed by laser confocal microscope. At same time, the activity of ALP in the cell culture medium was tested by ALP detecting reagent, and the expression of OCN in cell lysate was measured with ELISA method. Results The microfilament cytoskeleton depolymerization, reduction of tension fibers and disorder were observed in all but normal gravity group, especially in the simulated microgravity+0.5 μg/ml cytochalasin B group. Compared with normal gravity group, the activity of ALP and the expression of OCN in other groups were in decreased tendency (F=17.23, 121.91, P<0.01), of which significant difference was found between simulated microgravity+0.5 μg/ml cytochalasin B group and 0.5 μg/ml cytochalasin B group (P<0.05). Conclusion Microgravity affects the activity of ALP and the expression of OCN and these may be associated with the disruption of microfilament cytoskeleton that induced by simulated microgravity.