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作 者:张建新[1] 刘宇[1] 侯雯跻[1] 蒋海华[1] 祝文蕊 沈耀[1] 党胜春[1] 范昕[1]
出 处:《江苏医药》2013年第24期2962-2964,F0002,共4页Jiangsu Medical Journal
基 金:国家自然科学基金(81070287);镇江市科技计划项目(SH2011026;SH2012031)
摘 要:目的探讨胰腺星状细胞(PSCs)对胰腺癌细胞PANC-1迁移能力的影响。方法从小鼠胰腺组织中分离PSCs后分为A组(共培养PSCs及PANC-1细胞)和B组(PANC-1细胞),均以Transwell小室培养24h。细胞划痕及细胞迁移实验分别检测两组PANC-1细胞的迁徙距离和跨膜细胞数目,免疫荧光技术及Western blot测定两组PANC-1细胞中基质金属蛋白酶(MMP)-2和MMP-9的表达。结果培养24h后,A组细胞迁移距离远于B组[(18.75±1.70)mm vs.(12.40±1.14)mm](P<0.05),跨膜细胞数目多于B组[(137±24)个vs.(68±11)个](P<0.05),MMP-2和MMP-9蛋白表达量均高于B组(0.84±0.08vs.0.41±0.13和0.56±0.72vs.0.31±0.12)(P<0.05)。结论 PSCs能够增强PANC-1细胞迁移能力,促进PANC-1细胞中MMP-2、MMP-9的表达。Objective To explore the effects of pancreatic stellate cells(PSCs) on the migration of pancreatic cancer cells PANC-1. Methods PSCs deriveded from pancreatic tissue of mice were cultured for 24 h,which were assigned into two groups of A(PSCs and PANC1 co-cultured) and B (cultured with PANC-1 alone). Cell migration distance and transmembrane cell number of PANC-1 were detected by wound healing assay and migration assay, respectively. The expressions of matrix metalloproteinase(MMP)-2 and MMP-9 were detected by immunofluorescence technique and Western blot. Results After cultured for 24 h,cell migration distance of PANC-1 was farther in group A than that in group BE(18. 75±1.70) mm vs. (12.40±1.14) mini (P〈0. 05), transmembrane cell number of PANC-1 was more in group A than that in group B [(137 ± 24) pieces vs. (68 ±11) pieces] (P〈0. 05) ,and the expressions of MMP-2 and MMP-9 were higher in group A than those in group B (0.84±0.08 vs. 0.41±0.13 and 0.56±0.72 vs. 0.31±0.12)(P〈0.05),Conelusion PSCscan enhance the ability of PANC-1 to migrate, and promote the expressions of MMP-2 and MMP-9 in PANC-1.
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