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首页> 外文期刊>Cellular Physiology and Biochemistry >Growth/differentiation Factor-5 Induces Osteogenic Differentiation of Human Ligamentum Flavum Cells through Activation of ERK1/2 and p38 MAPK
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Growth/differentiation Factor-5 Induces Osteogenic Differentiation of Human Ligamentum Flavum Cells through Activation of ERK1/2 and p38 MAPK

机译:生长/分化因子-5通过激活ERK1 / 2和p38 MAPK诱导人黄韧带黄细胞的成骨分化

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摘要

Ossification of ligamentum flavum (OLF) is a pathological ectopic ossification in the spinal ligament, leading to spinal canal stenosis, but little was known about its pathogenesis. A previous study has found growth/differentiation factor (GDF)-5 expression at ossified sites of the ligaments from OLF patients. This study aimed to investigate the osteogenic effects of GDF-5 on cultured human ligamentum flavum cells (LFCs). LFCs were isolated from human spinal ligamentum flavum, and treated with or without recombinant human (rh) GDF-5. Alkaline phosphatase (ALP) activity was measured. Expression of osteocalcin was assessed by reverse transcriptase-PCR, Western blotting and immunofluorescence. Matrix mineralization was assessed by alizarin red staining. Activation of mitogen-activated protein kinases (MAPK) ERK1/2, p38 and JNK were detected by Western blotting. We found that rhGDF-5 treatment increased ALP activity and osteocalcin expression in a time- and dose-dependent manner, and induced mineralized nodule form. In addition, rhGDF-5 challenge mediated the ERK1/2 and p38 activation but not JNK. Inhibiting this activation pharmacologically, using U0126, a ERK1/2 inhibitor, or SB203580, a p38 inhibitor, resulted in significantly lower ALP activity and osteocalcin protein expression. The present study shows that rhGDF-5 induces osteogenic differentiation of human LFCs through activation of ERK1/2 and p38 MAPK. These findings give some new insight into the pathogenesis of OLF.
机译:黄韧带骨化症(OLF)是脊柱韧带中的一种病理性异位骨化症,可导致椎管狭窄,但对其发病机理知之甚少。先前的研究发现OLF患者韧带骨化部位的生长/分化因子(GDF)-5表达。这项研究旨在调查GDF-5对培养的人类韧带黄酮细胞(LFCs)的成骨作用。从人脊髓黄韧带分离LFC,并用或不用重组人(rh)GDF-5进行处理。测量碱性磷酸酶(ALP)的活性。骨钙素的表达通过逆转录-PCR,蛋白质印迹和免疫荧光进行评估。通过茜素红染色评估基质矿化。通过Western印迹检测丝裂原活化蛋白激酶(MAPK)ERK1 / 2,p38和JNK的活化。我们发现,rhGDF-5治疗以时间和剂量依赖性方式增加ALP活性和骨钙素表达,并诱导矿化结节形式。此外,rhGDF-5攻击介导ERK1 / 2和p38激活,但不介导JNK。使用U0126(一种ERK1 / 2抑制剂)或SB203580(一种p38抑制剂)在药理学上抑制这种激活可显着降低ALP活性和骨钙蛋白的表达。本研究表明,rhGDF-5通过激活ERK1 / 2和p38 MAPK诱导人LFC的成骨分化。这些发现为OLF的发病机理提供了新的见解。

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