Department of Biochemical Science and Technology, National Chiayi University, Chiayi City 60004, Taiwan.
Department of Food Science, National Chiayi University, Chiayi City 60004, Taiwan.
Cells. 2022 Aug 20;11(16):2600. doi: 10.3390/cells11162600.
Degenerative disc disease (DDD) is an important cause of low back pain. Repetitive tensile stress from the daily motion of the spine predisposes it to injury of the annulus fibrosus (AF) which causes IVD degeneration. This study aims to determine the causal relationship between mechanical stretch and osteogenesis in the AF cells of IVD as affected by bone morphogenic proteins (BMPs), specifically BMP-2/6 heterodimers. Our results found that 15% tensile stress (high cyclic stretching, HCS) may induce the expression of osteogenesis-related markers (Runx2, osterix) by upregulating BMP-2/6 heterodimeric ligands and their receptors on the human AF cell line. HCS also induced transient phosphorylation of p38 mitogen-activated protein (MAP) kinase and SMAD1/5/8. Neutralizing antibodies to the BMP-2/6 receptor (ALK3) blocked the expression of Runx2 and osterix, as well as the phosphorylation of p38 and SMAD1/5/8. In addition, treatment with a p38 MAPK inhibitor (SB203580) or siRNA to neutralize the effects of SMAD1/5/8 suppressed tensile stress-induced Runx2 and osterix expression. Mechanical stretching induces activation of p38 MAP kinase and SMAD1/5/8 signaling pathways, followed by the upregulation of BMP-2/6 heterodimer expression, thereby stimulating osteogenic Runx2 and osterix expression on AF cells. HCS may accelerate the progression of IVD degeneration by promoting an osteogenic response.
退变性椎间盘疾病(DDD)是腰痛的一个重要原因。脊柱日常运动产生的反复张应力使纤维环(AF)易于受伤,从而导致椎间盘退变。本研究旨在确定骨形态发生蛋白(BMPs),特别是 BMP-2/6 异二聚体对椎间盘 AF 细胞的机械拉伸和成骨作用之间的因果关系。我们的结果发现,15%的张应力(高循环拉伸,HCS)可能通过上调人 AF 细胞系中 BMP-2/6 异二聚体配体及其受体,诱导成骨相关标志物(Runx2、osterix)的表达。HCS 还诱导 p38 丝裂原激活蛋白(MAP)激酶和 SMAD1/5/8 的瞬时磷酸化。BMP-2/6 受体(ALK3)的中和抗体阻断了 Runx2 和 osterix 的表达,以及 p38 和 SMAD1/5/8 的磷酸化。此外,用 p38 MAPK 抑制剂(SB203580)或 siRNA 中和 SMAD1/5/8 的作用抑制了拉伸应力诱导的 Runx2 和 osterix 表达。机械拉伸诱导 p38 MAP 激酶和 SMAD1/5/8 信号通路的激活,继而上调 BMP-2/6 异二聚体的表达,从而刺激 AF 细胞的成骨 Runx2 和 osterix 表达。HCS 可能通过促进成骨反应加速椎间盘退变的进展。