摘要
目的:利用反义寡核着酸阻遏血管平滑肌细胞(VSMC)c-myC,PCNA基因表达,为移植血管再狭窄的基因治疗提供理论依据.方法:人工合成正义、反义及错配反义c-myc,PCNA基因片断,并转人体外培养的VSMC中,运用逆转录聚合酶链式反应(RT-PCR)测定细胞中相应基因表达的情况.结果:反义寡核苦酸能有效抑制VSMC中c-myc,PC-NA基因的表达,而正义和错配反义寡核着酸没有此效应.结论:反义寡核着酸能阻遏VSMC中相应基因的表达.
AIM: To provide the rationale for gene therapy oftransplanted vascular restenosis, antisense oligonucleotideswere applied to attenuate the expression of c--myc and proliferating cell nuclear antigen (PCNA ) genes in vascular smoothmuscle cells (VSMC ). METHODS: The antisense, sense,and mismatched oligonucleotides for c--m pc or PCNA geneswere synthesized and delivered individually to VSMC culturedin vitro. The expression of c--myc and PCNA genes was testedby reverse transcription and polymerase chain reaction (RTPCR) technique. RESULTS: The expression of c--m pc or PCNA genes decreased markedly in the VSMC treated with cmyc or PCNA antisense oligomers, whereas that treated withsense and mismatched oligomers did not. CONCLUSION: caac and PCNA genes antisense oligomers can reduce their related gene expression.
出处
《第四军医大学学报》
1999年第8期650-652,共3页
Journal of the Fourth Military Medical University
基金
国家自然科学基金!39470681
关键词
反义寡核苷酸
血管平滑肌
基因表达
血管移植
antisense oligonucleotide
smooth muscle, vascular
gene expression
protooncogene