华西口腔医学杂志
華西口腔醫學雜誌
화서구강의학잡지
WEST CHINA JOURNAL OF STOMATOLOGY
2015年
3期
234-237
,共4页
孙嵩%高强国%张纲%谭颖徽
孫嵩%高彊國%張綱%譚穎徽
손숭%고강국%장강%담영휘
神经生长因子%降钙素基因相关肽%细胞增殖
神經生長因子%降鈣素基因相關肽%細胞增殖
신경생장인자%강개소기인상관태%세포증식
nerve growth factor%calcitonin gene-related peptide%cell proliferation
目的:探讨创伤愈合过程中神经生长因子(NGF)调控降钙素基因相关肽(CGRP)的表达,以及影响MG-63细胞增殖的作用机制。方法加入不同质量浓度的NGF刺激MG-63细胞,1、2、3、4?d后收集样本,采用酶联免疫吸附测定法(ELISA)检测CGRP的表达,实时荧光定量聚合酶链反应(RT-QPCR)检测CGRP?mRNA的表达,采用细胞计数法(CCK-8)检测MG-63细胞的增殖;在MG-63细胞中加入NGF受体阻断剂,采用RT-QPCR和CCK-8检测CGRP?mRNA的表达及MG-63细胞的增殖效率。结果在NGF作用下,MG-63细胞分泌的CGRP表达量明显上调,随NGF质量浓度升高,CGRP表达量也相应升高,具有浓度依赖性,CGRP表达量随NGF作用时间延长也相应增加(P<0.05);随NGF质量浓度升高和作用时间延长,MG-63细胞的增殖效率也相应增加(P<0.05)。加入NGF受体阻断剂后此作用相应减弱(P<0.05)。结论在创伤愈合过程中NGF能通过上调CGRP的表达量影响MG-63细胞的增殖,从而促进创伤愈合。
目的:探討創傷愈閤過程中神經生長因子(NGF)調控降鈣素基因相關肽(CGRP)的錶達,以及影響MG-63細胞增殖的作用機製。方法加入不同質量濃度的NGF刺激MG-63細胞,1、2、3、4?d後收集樣本,採用酶聯免疫吸附測定法(ELISA)檢測CGRP的錶達,實時熒光定量聚閤酶鏈反應(RT-QPCR)檢測CGRP?mRNA的錶達,採用細胞計數法(CCK-8)檢測MG-63細胞的增殖;在MG-63細胞中加入NGF受體阻斷劑,採用RT-QPCR和CCK-8檢測CGRP?mRNA的錶達及MG-63細胞的增殖效率。結果在NGF作用下,MG-63細胞分泌的CGRP錶達量明顯上調,隨NGF質量濃度升高,CGRP錶達量也相應升高,具有濃度依賴性,CGRP錶達量隨NGF作用時間延長也相應增加(P<0.05);隨NGF質量濃度升高和作用時間延長,MG-63細胞的增殖效率也相應增加(P<0.05)。加入NGF受體阻斷劑後此作用相應減弱(P<0.05)。結論在創傷愈閤過程中NGF能通過上調CGRP的錶達量影響MG-63細胞的增殖,從而促進創傷愈閤。
목적:탐토창상유합과정중신경생장인자(NGF)조공강개소기인상관태(CGRP)적표체,이급영향MG-63세포증식적작용궤제。방법가입불동질량농도적NGF자격MG-63세포,1、2、3、4?d후수집양본,채용매련면역흡부측정법(ELISA)검측CGRP적표체,실시형광정량취합매련반응(RT-QPCR)검측CGRP?mRNA적표체,채용세포계수법(CCK-8)검측MG-63세포적증식;재MG-63세포중가입NGF수체조단제,채용RT-QPCR화CCK-8검측CGRP?mRNA적표체급MG-63세포적증식효솔。결과재NGF작용하,MG-63세포분비적CGRP표체량명현상조,수NGF질량농도승고,CGRP표체량야상응승고,구유농도의뢰성,CGRP표체량수NGF작용시간연장야상응증가(P<0.05);수NGF질량농도승고화작용시간연장,MG-63세포적증식효솔야상응증가(P<0.05)。가입NGF수체조단제후차작용상응감약(P<0.05)。결론재창상유합과정중NGF능통과상조CGRP적표체량영향MG-63세포적증식,종이촉진창상유합。
ObjectiveTo?investigate?the?nerve?growth?factor?(NGF)?regulating?the?expression?of?calcitonin?gene-related?peptide?(CGRP)?in?promoting?the?proliferation?of?osteoblast-like?cell?(MG-63)?and?thus?illustrate?the?mechanism?of?the?NGF?in?wound?healing.?Methods???Different?concentrations?of?NGF?were?used?to?stimulate?MG-63.?The?expression?of?CGRP?was?detected?by?real-time?quantitative?polymerase?chain?reaction?(RT-QPCR)?and?enzyme-linked?immunosorbent?assay?after?1,?2,?3,?and?4?days.?The?proliferation?of?MG-63?was?detected?by?cell?counting?kit-8?(CCK-8).?The?expression?of?CGRP?mRNA?and?the?proliferation?of?MG-63?were?then?detected?by?RT-QPCR?and?CCK-8?after?adding?the?NGF?receptor?blocker.?Results???Com-pared?with?the?blank?control?group,?the?expression?of?CGRP?significantly?increased?by?stimulating?the?NGF.?The?expression?of?CGRP?was?positively?related?to?the?concentration?of?NGF?(P<0.05).?Moreover,?the?expression?of?CGRP?increased?by?pro-longing?the?NGF?stimulation?time.?The?proliferation?of?MG-63?increased?after?stimulating?the?NGF?(P<0.05).?After?adding?the?NGF?receptor?blocker,?the?expression?of?CGRP?and?the?proliferation?of?MG-63?correspondingly?decreased?(P<0.05).?Conclusion???NGF?can?up-regulate?the?expression?of?CGRP?and?increase?the?proliferation?of?MG-63.?Therefore,?NGF?plays?a?significant?role?in?wound?healing.