Rmaidi Assia, Zelzer Mischa, Sindji Laurence, Dima Raphaël, Boury Frank, Delorme Nicolas, Montero-Menei Claudia N
CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France.
School of Pharmacy, Biodiscovery Institute, University Park, University of Nottingham, Nottingham NG7 2RD, United Kingdom.
Mater Sci Eng C Mater Biol Appl. 2021 Feb;121:111852. doi: 10.1016/j.msec.2020.111852. Epub 2021 Jan 6.
Polymeric, biodegradable, microspheres (MS) presenting a biomimetic surface of extracellular matrix (ECM) proteins are currently used for transporting cells and/or encapsulated proteins for regenerative medicine studies. They can be made of (lactic-co-glycolic acid) (PLGA) or of a more hydrophilic PLGA-P188 (Poloxamer188)-PLGA polymer allowing for the complete release of the therapeutic proteins. They promote stem cell adhesion, cell survival and differentiation after transplantation. Although the biological effectiveness of these microcarriers is established, a detailed understanding of the protein and cell interactions with the microcarrier surface remain unclear due to a lack of information of their surface properties. The aim of this study was to characterize the physicochemical properties of two polymeric MS systems and determine the effect of laminin and poly-d-lysine coated microcarriers on stem cell adhesion, survival and neuronal differentiation. The hydrophobicity and topography of PLGA MS promoted protein adsorption and the stem cells quickly adhered and spread on the surface of these microcarriers. In contrast less proteins adsorbed onto PLGA-P188-PLGA MS and although cells adhered to these microcarriers, they remained round and did not spread on their surface. Despite these early-stage differences, our results suggest that the nature of the MS does not strongly influence the long-term cell behavior. The cells exhibit the same cell number, differentiation profile and ability to secrete ECM molecules regardless of the type of microcarrier used. Likely the ECM molecules that form a microenvironment around both of these 3D microcarrier/cell constructs over time play a role in this converging cell behavior. We have thus furthered our understanding of the physicochemical properties of polymeric cell carriers affecting stem cell behavior to help tailor suitable microcarriers for neuroregenerative applications.
具有细胞外基质(ECM)蛋白仿生表面的聚合物可生物降解微球(MS)目前用于再生医学研究中运输细胞和/或封装蛋白质。它们可以由聚(乳酸-乙醇酸)(PLGA)或更具亲水性的PLGA-P188(泊洛沙姆188)-PLGA聚合物制成,能使治疗性蛋白质完全释放。它们能促进移植后干细胞的黏附、存活和分化。尽管这些微载体的生物学有效性已得到证实,但由于缺乏其表面性质的信息,对蛋白质和细胞与微载体表面相互作用的详细了解仍不清楚。本研究的目的是表征两种聚合物MS系统的物理化学性质,并确定层粘连蛋白和聚-D-赖氨酸包被的微载体对干细胞黏附、存活和神经元分化的影响。PLGA MS的疏水性和表面形貌促进了蛋白质吸附,干细胞迅速黏附并铺展在这些微载体表面。相比之下,较少的蛋白质吸附到PLGA-P188-PLGA MS上,尽管细胞黏附在这些微载体上,但它们仍保持圆形,没有在其表面铺展。尽管存在这些早期差异,但我们的结果表明,MS的性质对细胞的长期行为影响不大。无论使用何种类型的微载体,细胞都表现出相同的细胞数量、分化特征和分泌ECM分子的能力。随着时间的推移,在这两种3D微载体/细胞构建体周围形成微环境的ECM分子可能在这种趋同的细胞行为中发挥作用。因此,我们进一步了解了影响干细胞行为的聚合物细胞载体的物理化学性质,以帮助定制适合神经再生应用的微载体。