Halver Jonas, Wenzel Kristin, Sendker Jandirk, Carrillo García Carmen, Erdelmeier Clemens A J, Willems Erik, Mercola Mark, Symma Nico, Könemann Stephanie, Koch Egon, Hensel Andreas, Schade Dennis
Department of Chemistry and Chemical Biology, Technical University of Dortmund, Dortmund, Germany.
Department of Internal Medicine B, University Medicine Greifswald, Greifswald, Germany.
Front Pharmacol. 2019 Nov 27;10:1357. doi: 10.3389/fphar.2019.01357. eCollection 2019.
Extracts from the leaves and flowers of spp. (i.e., hawthorn species) have been traditionally used with documented preclinical and clinical activities in cardiovascular medicine. Based on reported positive effects on heart muscle after ischemic injury and the overall cardioprotective profile, the present study addressed potential contributions of extracts to cardiopoietic differentiation from stem cells. The quantified extract WS1442 stimulated cardiomyogenesis from murine and human embryonic stem cells (ESCs). Mechanistically, this effect was found to be induced by promoting differentiation of cardiovascular progenitor cell populations but not by proliferation. Bioassay-guided fractionation, phytochemical and analytical profiling suggested high-molecular weight ingredients as the active principle with at least part of the activity due to oligomeric procyanidines (OPCs) with a degree of polymerization between 3 and 6 (DP3-6). Transcriptome profiling in mESCs suggested two main, plausible mechanisms: These were early, stress-associated cellular events along with the modulation of distinct developmental pathways, including the upregulation of brain-derived neurotrophic factor (BDNF) and retinoic acid as well as the inhibition of transforming growth factor β/bone morphogenetic protein (TGFβ/BMP) and fibroblast growth factor (FGF) signaling. In addition, WS1442 stimulated angiogenesis in Sca-1 progenitor cells from adult mice hearts. These data provide evidence for a differentiation promoting activity of WS1442 on distinct cardiovascular stem/progenitor cells that could be valuable for therapeutic heart regeneration after myocardial infarction. However, the relevance of this new pharmacological activity of spp. remains to be investigated and active ingredients from bioactive fractions will have to be further characterized.
山楂属植物(即山楂种)的叶和花提取物传统上已被用于心血管医学,并有临床前和临床活动的文献记载。基于缺血性损伤后对心肌的报道的积极作用以及整体心脏保护作用,本研究探讨了山楂提取物对干细胞向心脏细胞分化的潜在贡献。定量的山楂提取物WS1442可刺激小鼠和人类胚胎干细胞(ESC)的心肌生成。从机制上讲,这种作用是通过促进心血管祖细胞群的分化而非增殖来诱导的。生物测定指导的分级分离、植物化学和分析图谱表明,高分子量成分是活性成分,至少部分活性归因于聚合度在3至6之间(DP3 - 6)的低聚原花青素(OPC)。对小鼠胚胎干细胞的转录组分析表明有两种主要的、合理的机制:这些是早期的、与应激相关的细胞事件以及对不同发育途径的调节,包括脑源性神经营养因子(BDNF)和视黄酸的上调以及转化生长因子β/骨形态发生蛋白(TGFβ/BMP)和成纤维细胞生长因子(FGF)信号通路的抑制。此外,WS1442可刺激成年小鼠心脏Sca - 1祖细胞的血管生成。这些数据为WS1442对不同心血管干/祖细胞的分化促进活性提供了证据,这对于心肌梗死后的治疗性心脏再生可能是有价值的。然而,山楂属植物这种新药理活性的相关性仍有待研究,生物活性部分的活性成分将必须进一步表征。