Zhong Zhao-Ming, Chen Jian-Ting, Zhang Yu, Zha Ding-Sheng, Lin Zhuo-Sheng, Zhao Cheng-Yi, Xu Jun-Chang, Li Tao, Xu Zi-Xing
Department of Orthopedic and Spinal Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Cell Physiol Biochem. 2010;26(2):179-86. doi: 10.1159/000320526. Epub 2010 Aug 24.
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.
黄韧带骨化(OLF)是脊柱韧带中的一种病理性异位骨化,可导致椎管狭窄,但其发病机制尚不清楚。先前的一项研究发现,在OLF患者韧带的骨化部位有生长/分化因子(GDF)-5表达。本研究旨在探讨GDF-5对培养的人黄韧带细胞(LFCs)的成骨作用。从人脊柱黄韧带中分离出LFCs,并用或不用重组人(rh)GDF-5进行处理。测量碱性磷酸酶(ALP)活性。通过逆转录酶-PCR、蛋白质印迹法和免疫荧光法评估骨钙素的表达。通过茜素红染色评估基质矿化。通过蛋白质印迹法检测丝裂原活化蛋白激酶(MAPK)ERK1/2、p38和JNK的激活情况。我们发现,rhGDF-5处理以时间和剂量依赖性方式增加了ALP活性和骨钙素表达,并诱导了矿化结节的形成。此外,rhGDF-5刺激介导了ERK1/2和p38的激活,但未介导JNK的激活。使用ERK1/2抑制剂U0126或p38抑制剂SB203580进行药理学抑制这种激活,导致ALP活性和骨钙素蛋白表达显著降低。本研究表明,rhGDF-5通过激活ERK1/2和p38 MAPK诱导人LFCs的成骨分化。这些发现为OLF的发病机制提供了一些新的见解。