Chatgilialoglu Alexandros, Rossi Martina, Alviano Francesco, Poggi Paola, Zannini Chiara, Marchionni Cosetta, Ricci Francesca, Tazzari Pier Luigi, Taglioli Valentina, Calder Philip C, Bonsi Laura
Remembrane Srl, Imola, Italy.
Department of Experimental, Diagnostic and Specialty Medicine, Unit of Histology, Embryology and Applied Biology, University of Bologna, Via Belmeloro 8, 40126, Bologna, Italy.
Stem Cell Res Ther. 2017 Feb 7;8(1):31. doi: 10.1186/s13287-017-0487-4.
The study of lipid metabolism in stem cell physiology has recently raised great interest. The role of lipids goes beyond the mere structural involvement in assembling extra- and intra-cellular compartments. Nevertheless, we are still far from understanding the impact of membrane lipidomics in stemness maintenance and differentiation patterns. In the last years, it has been reported how in vitro cell culturing can modify membrane lipidomics. The aim of the present work was to study the membrane fatty acid profile of mesenchymal stromal cells (MSCs) derived from human fetal membranes (hFM-MSCs) and to correlate this to specific biological properties by using chemically defined tailored lipid supplements (Refeed®).
Freshly isolated hFM-MSCs were characterized for their membrane fatty acid composition. hFM-MSCs were cultivated in vitro following a classical protocol and their membrane fatty acid profile at different passages was compared to the profile in vivo. A tailored Refeed® lipid supplement was developed with the aim of reducing the differences created by the in vitro cultivation and was tested on cultured hFM-MSCs. Cell morphology, viability, proliferation, angiogenic differentiation, and immunomodulatory properties after in vitro exposure to the tailored Refeed® lipid supplement were investigated.
A significant modification of hFM-MSC membrane fatty acid composition occurred during in vitro culture. Using a tailored lipid supplement, the fatty acid composition of cultured cells remained more similar to their in vivo counterparts, being characterized by a higher polyunsaturated and omega-6 fatty acid content. These changes in membrane composition had no effect on cell morphology and viability, but were linked with increased cell proliferation rate, angiogenic differentiation, and immunomodulatory properties. In particular, Refeed®-supplemented hFM-MSCs showed greater ability to express fully functional cell membrane molecules.
Culturing hFM-MSCs alters their fatty acid composition. A tailored lipid supplement is able to improve in vitro hFM-MSC functional properties by recreating a membrane environment more similar to the physiological counterpart. This approach should be considered in cell therapy applications in order to maintain a higher cell quality during in vitro passaging and to influence the outcome of cell-based therapeutic approaches when cells are administered to patients.
干细胞生理学中脂质代谢的研究近来引起了极大关注。脂质的作用不仅限于在组装细胞外和细胞内区室方面的结构参与。然而,我们距离理解膜脂质组学在干性维持和分化模式中的影响仍有很大差距。在过去几年中,已有报道称体外细胞培养可改变膜脂质组学。本研究的目的是研究源自人胎膜的间充质基质细胞(hFM-MSCs)的膜脂肪酸谱,并通过使用化学定义的定制脂质补充剂(Refeed®)将其与特定生物学特性相关联。
对新鲜分离的hFM-MSCs进行膜脂肪酸组成分析。hFM-MSCs按照经典方案进行体外培养,并将不同传代时的膜脂肪酸谱与体内谱进行比较。开发了一种定制的Refeed®脂质补充剂,旨在减少体外培养造成的差异,并在培养的hFM-MSCs上进行测试。研究了体外暴露于定制的Refeed®脂质补充剂后的细胞形态、活力、增殖、血管生成分化和免疫调节特性。
体外培养期间,hFM-MSC膜脂肪酸组成发生了显著改变。使用定制的脂质补充剂后,培养细胞的脂肪酸组成与体内对应物更相似,其特征是多不饱和脂肪酸和ω-6脂肪酸含量更高。膜组成的这些变化对细胞形态和活力没有影响,但与细胞增殖率增加、血管生成分化和免疫调节特性相关。特别是,补充Refeed®的hFM-MSCs表现出更强的表达全功能细胞膜分子的能力。
培养hFM-MSCs会改变其脂肪酸组成。定制的脂质补充剂能够通过重建更类似于生理对应物的膜环境来改善体外hFM-MSC的功能特性。在细胞治疗应用中应考虑这种方法,以便在体外传代过程中维持更高的细胞质量,并在将细胞给予患者时影响基于细胞的治疗方法的结果。