Qin Wei, Yang Lin, Chen Xiaotong, Ye Shanyu, Liu Aijun, Chen Dongfeng, Hu Kunhua
Research Center for Integrative Medicine, School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
Traditional Chinese Medicine Innovation Research Center, Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine, Shenzhen, China.
Int J Stem Cells. 2023 Aug 30;16(3):326-341. doi: 10.15283/ijsc22046. Epub 2023 Jun 30.
Osteoarthritis (OA) is a degenerative disease that leads to the progressive destruction of articular cartilage. Current clinical therapeutic strategies are moderately effective at relieving OA-associated pain but cannot induce chondrocyte differentiation or achieve cartilage regeneration. We investigated the ability of wedelolactone, a biologically active natural product that occurs in Eclipta alba (false daisy), to promote chondrogenic differentiation.
Real-time reverse transcription-polymerase chain reaction, immunohistochemical staining, and immunofluorescence staining assays were used to evaluate the effects of wedelolactone on the chondrogenic differentiation of mesenchymal stem cells (MSCs). RNA sequencing, microRNA (miRNA) sequencing, and isobaric tags for relative and absolute quantitation analyses were performed to explore the mechanism by which wedelolactone promotes the chondrogenic differentiation of MSCs. We found that wedelolactone facilitates the chondrogenic differentiation of human induced pluripotent stem cell-derived MSCs and rat bone-marrow MSCs. Moreover, the forkhead box O (FOXO) signaling pathway was upregulated by wedelolactone during chondrogenic differentiation, and a FOXO1 inhibitor attenuated the effect of wedelolactone on chondrocyte differentiation. We determined that wedelolactone reduces enhancer of zeste homolog 2 (EZH2)-mediated histone H3 lysine 27 trimethylation of the promoter region of to upregulate its transcription. Additionally, we found that wedelolactone represses miR-1271-5p expression, and that miR-1271-5p post-transcriptionally suppresses the expression of that is dependent on the binding of miR-1271-5p to the 3'-untranscribed region.
These results indicate that wedelolactone suppresses the activity of EZH2 to facilitate the chondrogenic differentiation of MSCs by activating the FOXO1 signaling pathway. Wedelolactone may therefore improve cartilage regeneration in diseases characterized by inflammatory tissue destruction, such as OA.
骨关节炎(OA)是一种导致关节软骨进行性破坏的退行性疾病。目前的临床治疗策略在缓解OA相关疼痛方面有一定效果,但不能诱导软骨细胞分化或实现软骨再生。我们研究了从白花蟛蜞菊中提取的具有生物活性的天然产物去甲蟛蜞菊内酯促进软骨形成分化的能力。
采用实时逆转录-聚合酶链反应、免疫组织化学染色和免疫荧光染色分析评估去甲蟛蜞菊内酯对间充质干细胞(MSC)软骨形成分化的影响。进行RNA测序、微小RNA(miRNA)测序和相对与绝对定量等压标记分析,以探究去甲蟛蜞菊内酯促进MSC软骨形成分化的机制。我们发现去甲蟛蜞菊内酯促进人诱导多能干细胞来源的MSC和大鼠骨髓MSC的软骨形成分化。此外,在软骨形成分化过程中,去甲蟛蜞菊内酯上调叉头框O(FOXO)信号通路,FOXO1抑制剂减弱了去甲蟛蜞菊内酯对软骨细胞分化的作用。我们确定去甲蟛蜞菊内酯减少了增强子结合蛋白2(EZH2)介导的组蛋白H3赖氨酸27在 启动子区域的三甲基化,从而上调其转录。此外,我们发现去甲蟛蜞菊内酯抑制miR-1271-5p的表达,且miR-1271-5p在转录后抑制 的表达,这依赖于miR-1271-5p与 3'非转录区域的结合。
这些结果表明,去甲蟛蜞菊内酯通过激活FOXO1信号通路抑制EZH2的活性,促进MSC的软骨形成分化。因此,去甲蟛蜞菊内酯可能改善以炎症组织破坏为特征的疾病如OA中的软骨再生。