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作 者:黄秋霞[1] 周后德[1] 杜巍[1] 何玉玲[1] 廖二元[1]
机构地区:[1]中南大学湘雅二医院代谢内分泌研究所
出 处:《中华老年医学杂志》2005年第10期775-778,共4页Chinese Journal of Geriatrics
基 金:国家自然科学基金资助项目(30400218)
摘 要:目的观察雌二醇和孕酮对人成骨细胞和人成骨肉瘤MG63细胞胰岛素受体底物(IRS)mRNA表达的影响。探讨雌、孕激素参与骨代谢的作用机制。方法用半定量RTPCR检测人成骨细胞和人成骨肉瘤细胞IRS1、IRS2mRNA的表达量。结果雌二醇或孕酮均诱导MG63细胞IRS2mRNA的表达上调,具有剂量依赖性(P<0.05)和时效依赖性(P<0.05)。其中分别以10-8mol/L的雌二醇干预24h和10-8mol/L的孕酮干预12h作用最明显,分别为对照组的(421±68)%和(327±54)%(均P<0.01)。雌二醇或孕酮共同干预进一步促进MG63细胞和人成骨细胞IRS2mRNA表达的上调,分别为对照组的(496±54)%和(452±58)%(均为P<0.01)。雌二醇和孕酮不影响人成骨细胞和MG63细胞IRS1mRNA的表达(P>0.05)。结论雌二醇或孕酮均可使人成骨细胞和MG63细胞的IRS2mRNA表达上调,且存在剂量与时间依赖性;但不影响IRS1mRNA的表达。Objective To characterize the effects of estradiol(E2 ) and progesterone (P) on the gene expression of IRS families in cultured normal human osteoblast-like cells (HOB) and human osteosarcoma cell line MG-63 in order to understand the mechanism of E2and P acting on the bone. Methods Semi-quantitative RT-PCR was used to study the action of E2 and P on the expression of mRNA of IRS family. Results 10^-10-10^-6 mol/I, of E2 and/or P could up-regulate the gene expression of IRS2 mRNA in a dose- and time-dependent manners in MG-63 cells(P〈0.05), the maximal effect to stimulate the expression of IRS-2 was in 10^-8mol/L at 24 h for E2 (421±68)%(P〈0.01), and 10 ^-8 M at 12h for P(327±54)% (P〈0.01). Combined intervention of E2 and P in MG-63 cells and HOB could further increase the expression of IRS-2 mRNA to(496 × 54)% (P〈0.01) and to(452±58)%(P〈0.01)versus the control, respectively. E and Phad no effects on the expression of IRS-1 mRNA in MG-63 cells or HOB. Conclusions E2 and P can dose and time dependently up-regulate the expression of IRS-2 mRNA in MG-63 cells and HOB. Combined intervention of E2 and P can positively create a synergistic effect on the up-regulation of IRS-2 mRNA. But E2 and P have no effects on the expression of IRS-1 mRNA in MG-63 cells or HOB.
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