Carlos Chagas Institute, R Prof Algacyr Munhoz Mader, FIOCRUZ, Curitiba, Brazil.
Exp Biol Med (Maywood). 2010 Aug;235(8):1015-24. doi: 10.1258/ebm.2010.010003.
The use of conditioned medium (CM) from human cardiac explants (HCEs) as a potential source of paracrine factors for adult stem cell signaling has never been evaluated. We hypothesized that HCEs might provide a source of soluble factors triggering the differentiation of mesenchymal stem cells (MSCs) into cardiomyocyte-like cells. By using two-dimensional electrophoresis (2-DE) gels/mass spectrometry and antibody macroarray assays, we found that HCEs release macromolecules, including cytokines, growth factors and myocardial and metabolism-related proteins into the culture medium. We identified a total of 20 proteins in the HCE-CM. However, as shown by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and 2-DE, these 20 proteins account for only a fraction of the total number of proteins present in the HCE-CM. We also found that CM increased the proliferation of bone marrow-derived-MSCs (BM-MSCs) in vitro. Unlike the other effects, this effect was most evident after 48 h of culture. Moreover, we examined the effect of HCE-CM on levels of mRNA and protein for specific cardiac markers. We showed that a surprisingly big fraction of BM-MSCs (3.4-5.0%) treated in vitro with HCE-CM became elongated and began to express cardiac markers, consistent with their possible differentiation into cardiomyocyte-like cells. Our in vitro model may be useful not only per se, but also for studies of the mechanisms of action of soluble factors involved in cell differentiation, paving the way for possible new protein-based treatments in the future.
从未有人评估过用人心脏组织块(HCE)的条件培养基(CM)作为成体干细胞信号转导的旁分泌因子的潜在来源。我们假设 HCE 可能提供一种来源的可溶性因子,可触发间充质干细胞(MSCs)分化为心肌样细胞。通过使用二维电泳(2-DE)凝胶/质谱和抗体宏阵列测定法,我们发现 HCE 将包括细胞因子、生长因子以及心肌和代谢相关蛋白在内的大分子释放到培养基中。我们在 HCE-CM 中总共鉴定出 20 种蛋白质。然而,如十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和 2-DE 所示,这 20 种蛋白质仅占 HCE-CM 中存在的蛋白质总数的一部分。我们还发现 CM 可增加骨髓来源的-MSCs(BM-MSCs)在体外的增殖。与其他作用不同,这种作用在培养 48 小时后最为明显。此外,我们研究了 HCE-CM 对特定心脏标志物的 mRNA 和蛋白水平的影响。我们发现,用 HCE-CM 体外处理的 BM-MSCs(3.4-5.0%)中有很大一部分呈长形并开始表达心脏标志物,这与它们可能分化为心肌样细胞一致。我们的体外模型不仅本身有用,而且还可用于研究参与细胞分化的可溶性因子的作用机制,为将来可能的新基于蛋白质的治疗方法铺平道路。