Ishidou Y, Tokunaga M, Murata F, Yoshida H, Sakou T
Department of Orthopaedic Surgery, Kagoshima University, Japan.
In Vivo. 1995 Sep-Oct;9(5):469-74.
Ossification of the posterior longitudinal ligament (OPLL) is an intractable disease developing into severe myelopathy and often accompanied by ossification of several other spinal ligaments and articular ligaments. Therefore, it is highly probable that predisposition to systemic ossification underlies the onset of this disease. Terayama et al(1981) reported that the nuchal skin of OPLL patients tended to be tougher than that of healthy individuals. Decorin is a component of the extracellular matrix which antagonistically regulates the action of Transforming growth factor-beta (TGF-beta). Imamura et al(1995) demonstrated immunohistochemically that decorin increased in the epidermis of the nuchal skin of OPLL patients. This suggests an abnormal expression of the extracellular matrix in the skin of OPLL patients. In the present study, in situ hybridization with non-radioactive synthetic oligodeoxynucleotide probes revealed an enhanced expression of decorin mRNA in the epidermal keratinocytes of OPLL patients. The increased expression of decorin mRNA in the epidermis of OPLL patients may be interpreted as reflecting abnormalities of the matrix associated with ossification of the ligaments. Studies on the role of decorin in ossification will contribute to clarification of the pathophysiology and pathogenesis of OPLL.
后纵韧带骨化症(OPLL)是一种难治性疾病,可发展为严重的脊髓病,且常伴有其他几种脊柱韧带和关节韧带的骨化。因此,全身性骨化的易感性很可能是该疾病发病的基础。寺山等人(1981年)报告称,OPLL患者的项部皮肤往往比健康人更坚韧。核心蛋白聚糖是细胞外基质的一种成分,可拮抗转化生长因子-β(TGF-β)的作用。今村等人(1995年)通过免疫组织化学方法证明,OPLL患者项部皮肤表皮中的核心蛋白聚糖增加。这表明OPLL患者皮肤中细胞外基质存在异常表达。在本研究中,使用非放射性合成寡脱氧核苷酸探针进行原位杂交显示,OPLL患者表皮角质形成细胞中核心蛋白聚糖mRNA的表达增强。OPLL患者表皮中核心蛋白聚糖mRNA表达的增加可能被解释为反映了与韧带骨化相关的基质异常。对核心蛋白聚糖在骨化中作用的研究将有助于阐明OPLL的病理生理学和发病机制。