The Second Spine Department, The Fourth School of Clinical Medicine of Xinjiang Medical University, Urumqi, 830000, China.
BMC Musculoskelet Disord. 2024 Apr 1;25(1):249. doi: 10.1186/s12891-024-07382-5.
This study investigated the role of Galectin-3 in the degeneration of intervertebral disc cartilage.
The patients who underwent lumbar spine surgery due to degenerative disc disease were recruited and divided into Modic I, Modic II, and Modic III; groups. HE staining was used to detect the pathological changes in endplates. The changes of Galectin-3, MMP3, Aggrecan, CCL3, and Col II were detected by immunohistochemistry, RT-PCR, and Western blot. MTT and flow cytometry were used to detect cartilage endplate cell proliferation, cell cycle, and apoptosis.
With the progression of degeneration (from Modic I to III), the chondrocytes and density of the cartilage endplate of the intervertebral disc decreased, and the collagen arrangement of the cartilage endplate of the intervertebral disc was broken and calcified. Meanwhile, the expressions of Aggrecan, Col II, Galectin-3, Aggrecan, and CCL3 gradually decreased. After treatment with Galectin-3 inhibitor GB1107, the proliferation of rat cartilage end plate cells was significantly reduced (P < 0.05). GB1107 (25 µmol/L) also significantly promoted the apoptosis of cartilage endplate cells (P < 0.05). Moreover, the percentage of cartilage endplate cells in the G1 phase was significantly higher, while that in the G2 and S phases was significantly lower (P < 0.05). Additionally, the mRNA and protein expression levels of MMP3, CCL3, and Aggrecan in rat cartilage end plate cells were lower than those in the control group.
Galectin-3 decreases with the progression of the cartilage endplate degeneration of the intervertebral disc. Galectin-3 may affect intervertebral disc degeneration by regulating the degradation of the extracellular matrix.
本研究探讨了半乳糖凝集素-3 在椎间盘软骨退变中的作用。
招募因退行性椎间盘疾病而行腰椎手术的患者,并将其分为 Modic I、Modic II 和 Modic III 组;采用 HE 染色检测终板的病理变化。通过免疫组织化学、RT-PCR 和 Western blot 检测 Galectin-3、MMP3、Aggrecan、CCL3 和 Col II 的变化。MTT 和流式细胞术检测软骨终板细胞增殖、细胞周期和凋亡。
随着退变的进展(从 Modic I 到 III),椎间盘软骨终板的软骨细胞和密度减少,软骨终板的胶原排列断裂和钙化。同时,Aggrecan、Col II、Galectin-3、Aggrecan 和 CCL3 的表达逐渐下降。用 Galectin-3 抑制剂 GB1107 处理后,大鼠软骨终板细胞的增殖明显减少(P<0.05)。GB1107(25 μmol/L)还明显促进软骨终板细胞的凋亡(P<0.05)。此外,软骨终板细胞 G1 期的比例明显升高,而 G2 和 S 期的比例明显降低(P<0.05)。此外,大鼠软骨终板细胞中 MMP3、CCL3 和 Aggrecan 的 mRNA 和蛋白表达水平均低于对照组。
随着椎间盘软骨终板退变的进展,Galectin-3 减少。Galectin-3 可能通过调节细胞外基质的降解来影响椎间盘退变。