Orthopedic Department, Faculdade de Medicina ABC, Santo André, São Paulo, Brazil.
Clinics (Sao Paulo). 2011;66(5):903-9. doi: 10.1590/s1807-59322011000500030.
To determine the molecules involved in extracellular matrix remodeling and to identify and quantify heparanase isoforms present in herniated and degenerative discs.
Heparanase is an endo-beta-glucuronidase that specifically acts upon the heparan sulfate chains of proteoglycans. However, heparanase expression in degenerative intervertebral discs has not yet been evaluated. Notably, previous studies demonstrated a correlation between changes in the heparan sulfate proteoglycan pattern and the degenerative process associated with intervertebral discs.
Twenty-nine samples of intervertebral degenerative discs, 23 samples of herniated discs and 12 samples of non-degenerative discs were analyzed. The expression of both heparanase isoforms (heparanase-1 and heparanase-2) was evaluated using immunohistochemistry and real-time RT-PCR analysis.
Heparanase-1 and heparanase-2 expression levels were significantly higher in the herniated and degenerative discs in comparison to the control tissues, suggesting a possible role of these proteins in the intervertebral degenerative process.
The overexpression of heparanase isoforms in the degenerative intervertebral discs and the herniated discs suggests a potential role of both proteins in the mediation of inflammatory processes and in extracellular matrix remodeling. The heparanase-2 isoform may be involved in normal metabolic processes, as evidenced by its higher expression in the control intervertebral discs relative to the expression of heparanase-1.
确定细胞外基质重塑涉及的分子,并鉴定和定量存在于突出和退行性椎间盘的肝素酶同工型。
肝素酶是一种内切-β-葡糖醛酸酶,特异性作用于蛋白聚糖的硫酸乙酰肝素链。然而,退行性椎间盘内的肝素酶表达尚未得到评估。值得注意的是,先前的研究表明,硫酸乙酰肝素蛋白聚糖模式的变化与椎间盘退行性过程之间存在相关性。
分析了 29 个退行性椎间盘样本、23 个椎间盘突出样本和 12 个非退行性椎间盘样本。使用免疫组织化学和实时 RT-PCR 分析评估了两种肝素酶同工型(肝素酶-1 和肝素酶-2)的表达。
与对照组织相比,突出和退行性椎间盘的肝素酶-1 和肝素酶-2 表达水平显著升高,提示这些蛋白可能在椎间盘退行性过程中发挥作用。
退行性和突出椎间盘中肝素酶同工型的过度表达表明这两种蛋白在介导炎症过程和细胞外基质重塑中可能发挥作用。肝素酶-2 同工型可能参与正常代谢过程,因为其在对照椎间盘中的表达高于肝素酶-1。