CTGF与VEGF-A在椎间盘纤维化进展中的相互作用。

Wangbing Xu, Jiqin Zhong, Jianrong Jian, Faming Zhong
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引用次数: 0

摘要

背景:髓核(NP)细胞外基质纤维化与椎间盘退变(IVDD)有关。结缔组织生长因子(CTGF)和血管内皮生长因子(VEGF)-A都是NP纤维化的病理基础。我们的研究目的是在体外NP细胞模型中验证CTGF与VEGF-A的相互作用。方法:收集不同变性程度的人NP组织,从未变性NP组织中分离NP细胞。分析自然变性NP和il -1β诱导变性NP细胞中CTGF和VEGF-A基因的表达。此外,通过外源蛋白处理、siRNA转染或特异性抑制剂干扰CTGF和VEGF-A的表达。免疫染色、western blotting和RT-PCR检测CTGF、VEGF-A、胶原I/II/III和聚集蛋白的蛋白或mRNA水平表达。结果:CTGF和VEGF-A在退行性变晚期较中期高表达,且表达具有协同作用。上调CTGF和VEGF-A中的一个可诱导另一个和I/III型胶原过表达,抑制II型胶原和聚集蛋白的表达;抑制其中一种蛋白可抑制另一种蛋白及I/III胶原蛋白的表达。结论:CTGF和VEGF-A在IVDD晚期升高。通过抑制其相互作用预防NP纤维化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The interaction between CTGF and VEGF-A in the progression of intervertebral disc fibrosis.

Background: Fibrosis in the extracellular matrix of nucleus pulposus (NP) is associated with intervertebral disc degeneration (IVDD). Both connective tissue growth factor (CTGF) and vascular endothelial growth factor (VEGF)-A are responsible for the pathological basis of NP fibrosis. Our study aims to verify the interaction between CTGF and VEGF-A in a vitro NP cell model.

Methodology: Collected human NP tissues of different degeneration degree and isolated the NP cells from the non-degenerated NP tissues. Analysed the CTGF and VEGF-A gene expression in the naturally degenerated NP and IL-1β-induced degenerated NP cells. Additionally, interfered wit the CTGF and VEGF-A expression by exogenic protein treatment, siRNA transfection, or specific inhibitor. The expression of CTGF, VEGF-A, collagen I/II/III and aggrecan with protein or mRNA level was determined by immunological staining, western blotting and RT-PCR.

Results: CTGF and VEGF-A highly expressed in the late-term of degeneration compared to the middle-term, and their expressions were synergistic. Upregulating one of CTGF and VEGF-A could induce the overexpression of the other one and collagen I/III, but suppressed collagen II and aggrecan expression; Besides, the suppression of one of them could inhibited another and collagen I/III expression.

Conclusions: CTGF and VEGF-A increase in late IVDD. Prevent NP fibrosis by suppressing their interaction.

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