颈、腰椎间盘组织tgfbeta1、bfgf、igf-1、ngf及基质金属蛋白酶iii基因mrna表达的比较

Ş. Yucetas, A. Yilmaz, E. Güleç, C. Ozic
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摘要

目的:评价和比较颈、腰椎退变椎间盘组织中抗氧化基因mRNA的表达。材料与方法:将获得的退变髓核(DNP)材料分为两组,分别为颈椎DNP (I组)(n=20)和腰椎DNP (II组)(n=20)。第一组男性6人,女性14人,平均年龄43.8岁;第二组男性13人,女性7人,平均年龄40.3岁(28 ~ 54岁)。所有颈椎DNP材料在C5和C6之间获得,所有腰椎DNP材料在L4和L5之间获得。采用聚合酶链反应、实时聚合酶链反应和western blotting技术检测DNP材料tgf - β1、bFGF、IGF-1、NGF和基质金属蛋白酶III (MMP III)基因的表达。结果:采用聚合酶链反应比较两组结果,发现腰椎DNP组tgf - β1、bFGF、IGF-1、NGF、MMP III表达较低。Real-time聚合酶链反应分析tgf - β1、bFGF、IGF-1、NGF和基质金属蛋白酶III基因表达水平下降。结论:这些数据表明;退变腰椎间盘组织中tgf - β1、bFGF、IGF-1、NGF和MMP III基因的减少,可能与疾病发病的分子背景有关。
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The comparison of the mrna expressions of tgfbeta1, bfgf, igf-1, ngf and matrix metalloprotease iii genes in cervical and lumbar disc tissues
Aim: To evaluate and compare the mRNA expression of antioxidant genes between the cervical and lumbar degenerated disc tissues. Material and Methods: Obtained degenerated Nucleus Pulposus (DNP) materials were divided into two groups, which were cervical DNP (Group I) (n=20) and lumbar DNP (Group II) (n=20). There are 6 men and 14 women in group I with a mean age of 43.8 years and 13 men and 7 women in group II with the mean age of 40.3 years (28 to 54). All cervical DNP materials were obtained between C5 and C6 and all lumbar DNP materials were obtained between L4 and L5 levels. The TGFβ1, bFGF, IGF-1, NGF and Matrix metalloprotease III (MMP III) gene expressions of DNP materials were determined by polymerase chain reaction, Real-time polymerase chain reaction and western blotting techniques.Results: When the results of the two groups were compared by polymerase chain reaction, the expressions of TGFβ1, bFGF, IGF-1, NGF and MMP III was found lower in lumbar DNP group. Also the TGFβ1, bFGF, IGF-1, NGF, and Matrix metalloprotease III genes showed a decrease in gene expression levels when they were analyzed by Real-time polymerase chain reaction. Conclusion: These data showed that; decrease of the TGFβ1, bFGF, IGF-1, NGF and MMP III genes in the degenerated lumbar disc tissues, may related with the possibility of molecular background of the disease pathogenesis.
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