脊柱外科杂志
脊柱外科雜誌
척주외과잡지
JOURNAL OF SPINE SURGERY
2014年
4期
248-251
,共4页
张伟军%冯虎%丁亚军%邓斌%蒋允昌%章浩杰%夏震
張偉軍%馮虎%丁亞軍%鄧斌%蔣允昌%章浩傑%夏震
장위군%풍호%정아군%산빈%장윤창%장호걸%하진
白细胞介素1β%肿瘤坏死因子α%基质金属蛋白酶类%聚合酶链反应
白細胞介素1β%腫瘤壞死因子α%基質金屬蛋白酶類%聚閤酶鏈反應
백세포개소1β%종류배사인자α%기질금속단백매류%취합매련반응
Interleukin-1beta%Tumor necrosis factor-alpha%Matrix metalloproteinases%Polymerase chain reaction
目的:探讨白细胞介素-1β( interleukin-1β,IL-1β)、肿瘤坏死因子-α( tumor necrosis factor-α,TNF-α)对髓核细胞的基质金属蛋白酶-28(matrix metalloproteinase-28, MMP-28)是否具有调控作用。方法培养人体正常髓核细胞,将3个不同浓度的IL-1β(0 ng/mL、10 ng/mL、50 ng/mL)和3个不同浓度的TNF-α(0 ng/mL、50 ng/mL、100 ng/mL)分别与体外扩增的第3代髓核细胞联合培养72 h,采用实时聚合酶链反应(real time-polymerase chain reaction , RT-PCR)法测定MMP-28 mRNA的转录水平,采用单因素方差分析法比较转录水平的差异。结果不同浓度(0 ng/mL、10 ng/mL、50 ng/mL)的IL-1β与髓核细胞共培养72 h后,各组间MMP-28mRNA转录水平(0.325±0.019、0.343±0.018、0.343±0.018)差异无统计学意义(P>0.05)。不同浓度(0 ng/mL、50 ng/mL、100 ng/mL)TNF-α与髓核细胞共培养72 h后,各组间MMP-28 mRNA转录水平(0.325±0.019、0.515±0.02、0.610±0.012)差异有统计学意义(P<0.01),且高浓度组MMP-28 mRNA转录水平较低浓度组明显升高(P<0.01)。结论 IL-1β对正常人体髓核细胞MMP-28转录无调控作用,而TNF-α可以上调MMP-28mRNA转录水平,且呈浓度依赖性。
目的:探討白細胞介素-1β( interleukin-1β,IL-1β)、腫瘤壞死因子-α( tumor necrosis factor-α,TNF-α)對髓覈細胞的基質金屬蛋白酶-28(matrix metalloproteinase-28, MMP-28)是否具有調控作用。方法培養人體正常髓覈細胞,將3箇不同濃度的IL-1β(0 ng/mL、10 ng/mL、50 ng/mL)和3箇不同濃度的TNF-α(0 ng/mL、50 ng/mL、100 ng/mL)分彆與體外擴增的第3代髓覈細胞聯閤培養72 h,採用實時聚閤酶鏈反應(real time-polymerase chain reaction , RT-PCR)法測定MMP-28 mRNA的轉錄水平,採用單因素方差分析法比較轉錄水平的差異。結果不同濃度(0 ng/mL、10 ng/mL、50 ng/mL)的IL-1β與髓覈細胞共培養72 h後,各組間MMP-28mRNA轉錄水平(0.325±0.019、0.343±0.018、0.343±0.018)差異無統計學意義(P>0.05)。不同濃度(0 ng/mL、50 ng/mL、100 ng/mL)TNF-α與髓覈細胞共培養72 h後,各組間MMP-28 mRNA轉錄水平(0.325±0.019、0.515±0.02、0.610±0.012)差異有統計學意義(P<0.01),且高濃度組MMP-28 mRNA轉錄水平較低濃度組明顯升高(P<0.01)。結論 IL-1β對正常人體髓覈細胞MMP-28轉錄無調控作用,而TNF-α可以上調MMP-28mRNA轉錄水平,且呈濃度依賴性。
목적:탐토백세포개소-1β( interleukin-1β,IL-1β)、종류배사인자-α( tumor necrosis factor-α,TNF-α)대수핵세포적기질금속단백매-28(matrix metalloproteinase-28, MMP-28)시부구유조공작용。방법배양인체정상수핵세포,장3개불동농도적IL-1β(0 ng/mL、10 ng/mL、50 ng/mL)화3개불동농도적TNF-α(0 ng/mL、50 ng/mL、100 ng/mL)분별여체외확증적제3대수핵세포연합배양72 h,채용실시취합매련반응(real time-polymerase chain reaction , RT-PCR)법측정MMP-28 mRNA적전록수평,채용단인소방차분석법비교전록수평적차이。결과불동농도(0 ng/mL、10 ng/mL、50 ng/mL)적IL-1β여수핵세포공배양72 h후,각조간MMP-28mRNA전록수평(0.325±0.019、0.343±0.018、0.343±0.018)차이무통계학의의(P>0.05)。불동농도(0 ng/mL、50 ng/mL、100 ng/mL)TNF-α여수핵세포공배양72 h후,각조간MMP-28 mRNA전록수평(0.325±0.019、0.515±0.02、0.610±0.012)차이유통계학의의(P<0.01),차고농도조MMP-28 mRNA전록수평교저농도조명현승고(P<0.01)。결론 IL-1β대정상인체수핵세포MMP-28전록무조공작용,이TNF-α가이상조MMP-28mRNA전록수평,차정농도의뢰성。
Objective To investigate whether matrix metauoproteirase-28 ( MMP-28 ) can be regulated by interleubin-β( IL-1β) and tumor necrcsis factor-α( TNF-α) in human nucleus pulposus cells after coculture .Methods After the third gen-eration of human nucleus pulposus cells were stimulated with different concentration of IL -1β(0 ng/mL,10 ng/mL,50 ng/mL) and TNF-α(0 ng/mL,50 ng/mL,100 ng/mL) 72 h in vitro, MMP-28 mRNA was quantified by RT-PCR,the difference between each concentration were compared by one-way analysis of variance .Results There was no sign indicated that the various concentration of IL-1β(0 ng/mL,10 ng/mL,50 ng/mL) can affect human nucleus pulposus cells MMP-28 transcrip-tion (0.325 ±0.019 vs.0.343 ±0.018 vs.0.343 ±0.018, P>0.05).But cytokines TNF-αcould induce the expression of MMP-28, various concentration groups present significant difference (0.325 ±0.019 vs.0.515 ±0.02 vs.0.610 ±0.012, P<0.01), and with the concentration increasing , the effect was more prominent (0.610 ±0.012 vs.0.515 ±0.02, P<0.01).Conclusion IL-1βdoesn’t affect human nucleus pulposus cells MMP-28 transcription in vitro.However, TNF-αcan up regulate the MMP-28 mRNA of the nucleus pulposus cells and the effects are strengthened by enhancing concentration .