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首页> 外文期刊>DNA and Cell Biology >PPAR gamma-2 and BMPR2 Genes Were Differentially Expressed in Peripheral Blood of SLE Patients with Osteonecrosis
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PPAR gamma-2 and BMPR2 Genes Were Differentially Expressed in Peripheral Blood of SLE Patients with Osteonecrosis

机译:PPARγ-2和BMPR2基因在SLE患者的外周血液中差异表达,骨折坏死患者

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摘要

Most researchers believe that the peroxisome proliferative activated receptor gamma (PPAR gamma-2) and bone morphogenetic protein receptor type II (BMPR2) play important roles in steroid-induced osteonecrosis (ON). However, the molecular mechanism of this process is still unclear. Recent studies indicate that steroid treatments cause adipocyte formation due to differentiation of mesenchymal stem cells, which then prevents osteoblast formation. This study examined PPAR gamma-2, bone morphogenetic protein 2 (BMP2), and BMPR2 in patients with systemic lupus erythromatosus (SLE) who eventually developed ON after prolonged steroid treatment. The subjects of this experiment included 220 SLE patients who had undergone steroid treatment for at least 2 years. Fifty-five of the 220 patients were ON patients, and 165 were non-ON patients. Real-time PCR was performed to analyze the expression of the PPAR gamma-2, BMP2, and BMPR2 mRNA in the peripheral blood of these patients. The results indicated that the expression of PPAR gamma-2 mRNA increased 37% in the ON patients' peripheral blood, but the expression of BMPR2 mRNA decreased 57%. The average expression of the PPAR gamma-2 mRNA in the ON patients was significantly higher than that in the non-ON patients (p=0.044). Conversely, the expression of BMPR2 mRNA was significantly lower than that in non-ON patients (p=0.036), but the expression of BMP2 mRNA did not significantly differ. This study demonstrated that the PPAR gamma-2 and BMPR2 have important roles in the ON process after prolonged steroid administration in SLE patients; however, the detailed molecular mechanisms of this process require further study.
机译:大多数研究人员认为过氧化物体增殖活化受体γ(PPARγ-2)和骨形态发生蛋白受体类型II型(BMPR2)在类固醇诱导的骨折(ON​​)中起重要作用。然而,该过程的分子机制尚不清楚。最近的研究表明,类固醇处理引起由于间充质干细胞的分化引起的脂肪细胞形成,然后是防止成骨细胞形成。本研究检测了在延长类固醇治疗后最终开发的全身狼疮红细胞患者(SLE)的PPARγ-2,骨形态发生蛋白2(BMP2)和BMPR2。该实验的主题包括220名SLE患者,该患者经历了至少2年的类固醇治疗。 220名患者中55名患者,165例是非患者。进行实时PCR以分析这些患者的外周血中PPARγ-2,BMP2和BMPR2 mRNA的表达。结果表明,PPARγ-2 mRNA的表达在患者的外周血中增加了37%,但BMPR2 mRNA的表达降低了57%。对患者的PPARγ-2 mRNA的平均表达明显高于非对患者(P = 0.044)。相反,BMPR2 mRNA的表达明显低于非对患者(P = 0.036),但BMP2 mRNA的表达没有显着不同。本研究表明,PPARγ-2和BMPR2在SLE患者延长类固醇施用后的ON过程中具有重要作用;然而,该过程的详细分子机制需要进一步研究。

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