安徽医科大学学报
安徽醫科大學學報
안휘의과대학학보
ACTA UNIVERSITY MEDICINALIS ANHUI
2015年
5期
608-611
,共4页
高杰%桂斌捷%胡孔足%王斯晟
高傑%桂斌捷%鬍孔足%王斯晟
고걸%계빈첩%호공족%왕사성
环氧化酶-2%塞来昔布%成骨细胞%异位骨化
環氧化酶-2%塞來昔佈%成骨細胞%異位骨化
배양화매-2%새래석포%성골세포%이위골화
COX-2%celecoxib%osteoblasts%heterotopic ossification
目的:观察塞来昔布对人成骨细胞增殖的影响及其作用机制。方法将人成骨细胞分为3个组:空白对照组、IL-1刺激组(阴性对照组)、塞来昔布+ IL-1刺激组(药物干预组),用 RT-PCR 法和 Western blot 法分别检测三组成骨细胞环氧化酶-2( COX-2)、膜相关前列腺素 E2合成酶1(mPGES-1) mRNA 和蛋白的表达。 MTT 法检测塞来昔布对阴性对照组人成骨细胞增殖的影响。结果 RT-PCR 法和Western blot 法实验结果显示,同空白对照组相比,阴性对照组的人成骨细胞中 COX-2、mPGES-1 mRNA 和蛋白的表达均增加;同阴性对照组相比,药物干预组的 COX-2、mPGES-1 mRNA 和蛋白的表达均降低。塞来昔布对 IL-1刺激的人成骨细胞的生长具有抑制作用,呈现剂量依赖性,浓度越大,抑制作用越大;并且随着作用时间的延长,细胞的抑制作用增大。结论塞来昔布可以抑制炎性状态下人成骨细胞的生长,可能是通过调控 COX-2、mPGES-1 mRNA 和蛋白的表达,使其表达下调而发挥作用。
目的:觀察塞來昔佈對人成骨細胞增殖的影響及其作用機製。方法將人成骨細胞分為3箇組:空白對照組、IL-1刺激組(陰性對照組)、塞來昔佈+ IL-1刺激組(藥物榦預組),用 RT-PCR 法和 Western blot 法分彆檢測三組成骨細胞環氧化酶-2( COX-2)、膜相關前列腺素 E2閤成酶1(mPGES-1) mRNA 和蛋白的錶達。 MTT 法檢測塞來昔佈對陰性對照組人成骨細胞增殖的影響。結果 RT-PCR 法和Western blot 法實驗結果顯示,同空白對照組相比,陰性對照組的人成骨細胞中 COX-2、mPGES-1 mRNA 和蛋白的錶達均增加;同陰性對照組相比,藥物榦預組的 COX-2、mPGES-1 mRNA 和蛋白的錶達均降低。塞來昔佈對 IL-1刺激的人成骨細胞的生長具有抑製作用,呈現劑量依賴性,濃度越大,抑製作用越大;併且隨著作用時間的延長,細胞的抑製作用增大。結論塞來昔佈可以抑製炎性狀態下人成骨細胞的生長,可能是通過調控 COX-2、mPGES-1 mRNA 和蛋白的錶達,使其錶達下調而髮揮作用。
목적:관찰새래석포대인성골세포증식적영향급기작용궤제。방법장인성골세포분위3개조:공백대조조、IL-1자격조(음성대조조)、새래석포+ IL-1자격조(약물간예조),용 RT-PCR 법화 Western blot 법분별검측삼조성골세포배양화매-2( COX-2)、막상관전렬선소 E2합성매1(mPGES-1) mRNA 화단백적표체。 MTT 법검측새래석포대음성대조조인성골세포증식적영향。결과 RT-PCR 법화Western blot 법실험결과현시,동공백대조조상비,음성대조조적인성골세포중 COX-2、mPGES-1 mRNA 화단백적표체균증가;동음성대조조상비,약물간예조적 COX-2、mPGES-1 mRNA 화단백적표체균강저。새래석포대 IL-1자격적인성골세포적생장구유억제작용,정현제량의뢰성,농도월대,억제작용월대;병차수착작용시간적연장,세포적억제작용증대。결론새래석포가이억제염성상태하인성골세포적생장,가능시통과조공 COX-2、mPGES-1 mRNA 화단백적표체,사기표체하조이발휘작용。
Objective To study the impact of celecoxib on proliferation of human osteoblasts. Methods The hu-man osteoblasts were cultured and divided into three groups,including the negative control, positive control (stimu-lated by IL-1) and intervention group (celecoxib + IL-1). The detection of mRNA and protein level of COX-2 and mPGES-1 were measured by real tmie PCR (RT-PCR) and Western blot. MTT assay was performed to determine the impact of celecoxib on proliferation of human osteoblasts which were treated with IL-1. Results RT-PCR and Western blot showed that the detection of mRNA and protein level of COX-2 and mPGES-1 of the positive control (stimulated by IL-1) were significantly higher than that of the negative control and intervention group (celecoxib +IL-1). Celecoxib had cytotoxic effect on the growth of osteoblasts, manifests dose dependence as well as increasing cell inhibition over time. Conclusion Celecoxib could inhibit proliferation of osteoblasts, and could inhibit the oc-currence of heterotopic ossification by regulating the level of mPGES-1 and COX-2 mRNA and protein.