摘要
目的:以人原始巨核白血病细胞系(HIMeg)和人骨肉瘤细胞系(HOS-8603)为细胞模型,研究1,25一二羟维生素D3[1,25(OH)2D3]对维生素D3受体(VDR)mRNA表达的调节作用。方法:VDRmRNA的检测采用定量逆转录.聚合酶链反应(RT-PCR)。结果:HOS-8603细胞经1,25(OH)2D3处理0~24h后,VDRZRNA表达水平无明显变化;但是1,25(OH)2D3却可以使HIMeg细胞VDRmRNA水平明显降低,且具有时间依赖性,24h后达到最低水平,仅为对照组的15%。结论:1,25(OH)2D3对VDRmRNA表达的调节作用具有组织细胞特异性。
To explore the potential regulatory effects of 1, 25-dihydroxyvitamin D, L1' 25 (0H),D,j on the expression of vitamln D, receptor (VDR ) mRNA in human megakaryoblastic leukemia(HIMeg) and human osteosarcoma (HOS-86O3) cell lines. Methods: VDR mRNA expression was deter-mined by the utilization of our recently established quantitative reverse-transcripti0n p0lymerase chain re-acti0n (RT^PCR) method. Results: lt was found that VDR mRNA expression in HOS-86O3 cells was notchanged significantly after treatment with 1, 25 (OH),D, for O~ 24 h- On the other hand, treatment 0fHIMeg ce1ls with 1, 25 (OH),D, cou1d significantly induce a d0wn-regulati0n of VDR mRNA expressi0n ina time-dependent manner, reaching a level of about only 15% of control after 24 h treatment. C0ncIusi0n:The regulation of VDR mRNA expressi0n by 1,25 (OH), D, is of tissue-specific fashi0n.
出处
《第二军医大学学报》
CAS
CSCD
北大核心
1997年第1期32-34,共3页
Academic Journal of Second Military Medical University
基金
国家自然科学基金!39100051
39370303
关键词
二羟维生素D3
受体
MRNA
基因表达
1 , 25-dihydroxyvitamin D_3
receptor, 1, 25-dihydroxyvitamin D_3
mRNA
gene expression
RT-PCR