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唑来膦酸脉冲治疗可使骨髓间充质干细胞持续定向分化为成骨细胞。

Pulse treatment with zoledronic acid causes sustained commitment of bone marrow derived mesenchymal stem cells for osteogenic differentiation.

作者信息

Ebert Regina, Zeck Sabine, Krug Ralf, Meissner-Weigl Jutta, Schneider Doris, Seefried Lothar, Eulert Jochen, Jakob Franz

机构信息

Orthopedic Department, Orthopedic Center for Musculoskeletal Research, University of Würzburg, Würzburg, Germany.

出版信息

Bone. 2009 May;44(5):858-64. doi: 10.1016/j.bone.2009.01.009. Epub 2009 Jan 23.

Abstract

The aminobisphosphonate zoledronic acid (ZA) is a bone seeking specific inhibitor of protein farnesylation and geranylgeranylation, which causes inhibition of osteoclast function and apoptosis. It is widely used as an osteoclast targeted antiresorptive treatment of metastatic bone disease, Paget's disease and osteoporosis. Mesenchymal stem cells (MSC) and osteoblast precursors can also be targets of bisphosphonates, but the clinical relevance of these effects is under debate. We show here that ZA in vitro causes inhibition of proliferation and induction of apoptosis in hMSC, when applied in concentrations of 20 and 50 microM for more than 24 h which can be rescued by treatment with 10 microM geranylgeranyl pyrophosphate (GGPP). However, pulse stimulation for 3 and 6 h with these concentrations and subsequent culture for up to 2 weeks under osteogenic conditions exerts sustained regulation of osteogenic marker genes in hMSC. The effect on gene regulation translates into marked enhancement of mineralization, as shown by alizarin red and alkaline phosphatase staining after 4 weeks of osteogenic culture. ZA, when applied as a pulse stimulus, might therefore also stimulate osteogenic differentiation in vivo, since muM plasma concentrations can be achieved by intravenous application of 5 mg in patients. These data set the stage for the future dissection of the effects of ZA and other aminobisphosphonates on cells beyond osteoclasts, with respect to cell differentiation in benign metabolic and to antitumor efficacy in metastatic bone diseases, as well as adverse events due to putative substance accumulation in bone during long-term treatment.

摘要

氨基双膦酸盐唑来膦酸(ZA)是一种靶向骨组织的蛋白质法尼基化和香叶基香叶基化特异性抑制剂,可抑制破骨细胞功能并诱导其凋亡。它被广泛用作转移性骨病、佩吉特病和骨质疏松症的靶向破骨细胞抗吸收治疗药物。间充质干细胞(MSC)和成骨细胞前体也可能是双膦酸盐的作用靶点,但这些作用的临床相关性仍存在争议。我们在此表明,体外应用浓度为20和50微摩尔的ZA超过24小时会抑制人MSC的增殖并诱导其凋亡,而用10微摩尔香叶基香叶基焦磷酸(GGPP)处理可挽救这种情况。然而,用这些浓度进行3小时和6小时的脉冲刺激,随后在成骨条件下培养长达2周,会对人MSC中的成骨标记基因产生持续调控。对基因调控的影响转化为矿化的显著增强,成骨培养4周后茜素红和碱性磷酸酶染色显示了这一点。因此,当作为脉冲刺激应用时,ZA可能也会在体内刺激成骨分化,因为在患者中静脉注射5毫克ZA可达到微摩尔级的血浆浓度。这些数据为未来剖析ZA和其他氨基双膦酸盐对破骨细胞以外细胞的影响奠定了基础,这涉及良性代谢中的细胞分化、转移性骨病中的抗肿瘤疗效,以及长期治疗期间由于假定的物质在骨中积累而导致的不良事件。

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