Duarte-Olivenza Cristina, Montero Juan Antonio, Lorda-Diez Carlos Ignacio
Departamento de Anatomía y Biología Celular and IDIVAL, Universidad de Cantabria, Santander, 39011, Spain.
J Inflamm Res. 2021 Sep 29;14:5001-5011. doi: 10.2147/JIR.S324292. eCollection 2021.
Berberine (BBR) is an isoquinoline plant alkaloid with demonstrated anti-inflammatory, anti-tumor and immunosuppressive pharmacological properties that functions via multiple signaling pathways and epigenetic modulators. Numerous studies have proposed BBR as a promising therapeutic agent for joint cartilage degeneration, and other connective tissue diseases.
This work aimed to evaluate the effects of BBR on the growth and differentiation of embryonic skeletal progenitors using the limb mesoderm micromass culture assay.
Our findings show that at difference of its apoptotic influence on a variety of tumor tissues, cell death was not induced in skeletal progenitors by the addition of 12 or 25 µM BBR concentration to the culture medium. Morphological and transcriptional analysis revealed dual and opposite effects of BBR treatments on chondrogenesis depending on the stage of differentiation of the cultured progenitors. At early stage of culture, BBR was a potent chondrogenic inhibitor, while chondrogenesis was intensified in treatments at advanced stages of culture. The chondrogenic promoting effect was accompanied by a moderate upregulation of gene markers of prehypertrophic cartilage, including , alkaline phosphatase , and Indian Hedgehog . We further observed a positive transcriptional influence of BBR in the expression of DNA methyltransferase genes, and , suggesting a potential involvement of epigenetic factors in its effects.
Our study uncovers a new pharmacological influence of BBR in cartilage differentiation that must be taken into account in designing clinical protocols for its employment in the treatment of cartilage degenerative diseases.
黄连素(BBR)是一种异喹啉类植物生物碱,具有抗炎、抗肿瘤和免疫抑制药理特性,可通过多种信号通路和表观遗传调节剂发挥作用。众多研究已提出BBR有望成为治疗关节软骨退变及其他结缔组织疾病的药物。
本研究旨在利用肢体中胚层微团培养试验评估BBR对胚胎骨骼祖细胞生长和分化的影响。
我们的研究结果表明,与BBR对多种肿瘤组织的凋亡影响不同,向培养基中添加12或25μM浓度的BBR不会诱导骨骼祖细胞死亡。形态学和转录分析显示,根据培养祖细胞的分化阶段,BBR处理对软骨形成具有双重且相反的作用。在培养早期,BBR是一种有效的软骨形成抑制剂,而在培养后期的处理中软骨形成增强。软骨形成促进作用伴随着前肥大软骨基因标志物的适度上调,包括碱性磷酸酶和印度刺猬因子。我们进一步观察到BBR对DNA甲基转移酶基因和的表达具有正向转录影响,表明表观遗传因素可能参与其作用。
我们的研究揭示了BBR在软骨分化中的一种新的药理作用,在设计其用于治疗软骨退行性疾病的临床方案时必须考虑这一点。