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首页> 外文期刊>Calcified tissue international. >Uni-axial cyclic stretch induces Cbfa1 expression in spinal ligament cells derived from patients with ossification of the posterior longitudinal ligament.
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Uni-axial cyclic stretch induces Cbfa1 expression in spinal ligament cells derived from patients with ossification of the posterior longitudinal ligament.

机译:单轴循环拉伸诱导源自后纵韧带骨化症患者的脊髓韧带细胞中Cbfa1表达。

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摘要

Ossification of the posterior longitudinal ligament of the spine (OPLL) is characterized by ectopic bone formation in the spinal ligaments. Mechanical stress, which acts on the posterior ligaments, is thought to be an important factor in the progression of OPLL. To clarify this mechanism, we investigated the effects of in vitro cyclic stretch (120% peak to peak, at 0.5 Hz) on cultured spinal ligament cells derived from OPLL (OPLL cells) and non-OPLL (non-OPLL cells) patients. The mRNA expressions of Cbfa1 (an osteoblast-specific transcription factor), type I collagen, alkaline phosphatase (ALP), osteocalcin and integrin beta1 (a mechanotransducer) were increased by cyclic stretch in OPLL cells, whereas no change was observed in non-OPLL cells. The effects of cyclic stretch on the spinal ligament tissues derived from OPLL and non-OPLL patients were also analyzed by immunohistochemistry using an antibody against Cbfa1. The expression of Cbfa1 was increased by cyclic stretch at the center of the spinal ligament tissues of OPLL patients, whereas no change was observed in the tissues of non-OPLL patients. Furthermore, U0126, a specific inhibitor of MAPK kinase (MEK), suppressed the stretch-induced mRNA expressions of Cbfa1, ALP and type I collagen in OPLL cells. These results suggest that in OPLL cells, mechanical stress is converted by integrin beta1 into intracellular signaling and that Cbfa1 is activated through the MAP kinase pathway. Therefore, we propose that mechanical stress plays a key role in the progression of OPLL through an increase in Cbfa1 expression.
机译:脊柱后纵韧带骨化(OPLL)的特征是脊椎韧带中的异位骨形成。作用于后韧带的机械应力被认为是OPLL进展的重要因素。为了阐明该机制,我们研究了体外循环拉伸(在0.5 Hz处峰到峰的120%,在0.5 Hz时)对源自OPLL(OPLL细胞)和非OPLL(非OPLL细胞)患者的培养的脊髓韧带细胞的影响。 Cbfa1(成骨细胞特异性转录因子),I型胶原蛋白,碱性磷酸酶(ALP),骨钙素和整联蛋白β1(机械转导子)的mRNA表达通过循环拉伸在OPLL细胞中增加,而在非OPLL中未观察到变化细胞。还使用抗Cbfa1抗体通过免疫组织化学分析了循环拉伸对源自OPLL和非OPLL患者的脊髓韧带组织的影响。 Cbfa1的表达在OPLL患者的脊髓韧带组织中心通过周期性拉伸而增加,而在非OPLL患者的组织中未观察到变化。此外,U0126,一种MAPK激酶(MEK)的特异性抑制剂,抑制了OPLL细胞中由拉伸诱导的Cbfa1,ALP和I型胶原的mRNA表达。这些结果表明,在OPLL细胞中,机械应力由整联蛋白beta1转换为细胞内信号传导,并且Cbfa1通过MAP激酶途径被激活。因此,我们建议机械应力通过Cbfa1表达的增加在OPLL的进展中起关键作用。

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