Institute of Chemistry, University of Campinas (UNICAMP), Campinas, SP 13083-970, Brazil.
Univ Lyon, Université Claude Bernard Lyon 1, INSERM, Stem Cell and Brain Research Institute U1208, 69500 Bron, France.
Biomacromolecules. 2020 Aug 10;21(8):3394-3410. doi: 10.1021/acs.biomac.0c00825. Epub 2020 Jul 9.
Improving cell-material interactions of nonadhesive scaffolds is crucial for the success of biomaterials in tissue engineering. Due to their high surface area and open pore structure, sponges are widely reported as absorbent materials for biomedical engineering. The biocompatibility and biodegradability of polysaccharide sponges, coupled with the chemical functionalities of supramolecular dimers, make them promising combinations for the development of adhesive scaffolds. Here, a supramolecular tactic based on (UPy)-modified polysaccharide associated with three-dimensional structure of sponges was developed to reach enhanced cellular adhesion. For this purpose, three approaches were examined individually in order to accomplish this goal. In the first approach, the backbone polysaccharides with noncell adhesive properties were modified via a modular tactic using UPy-dimers. Hereupon, the physical-chemical characterizations of the supramolecular sponges were performed, showing that the presence of supramolecular dimers improved their mechanical properties and induced different architectures. In addition, small-angle neutron scattering (SANS) measurements and rheology experiments revealed that the UPy-dimers into agarose backbone are able to reorganize in thinning aggregates. It is also demonstrated that the resulted UPy-agarose (AGA-UPy) motifs in surfaces can promote cell adhesion. Finally, the last approach showed the great potential for use of this novel material in bioadhesive scaffolds indicating that neural stem cells show a spreading bias in soft materials and that cell adhesion was enhanced for all UPy-modified sponges compared to the reference, i.e. unmodified sponges. Therefore, by functionalizing sponge surfaces with UPy-dimers, an adhesive supramolecular scaffold is built which opens the opportunity its use neural tissues regeneration.
提高非黏附支架的细胞-材料相互作用对于生物材料在组织工程中的成功至关重要。由于其高表面积和开放的孔结构,海绵广泛被报道为生物医学工程的吸收材料。多糖海绵的生物相容性和可生物降解性,加上超分子二聚体的化学功能,使它们成为开发黏附支架的有前途的组合。在这里,基于(UPy)修饰的多糖与海绵的三维结构相关的超分子策略被开发用于增强细胞黏附。为此,分别检查了三种方法以实现这一目标。在第一种方法中,通过使用 UPy-二聚体的模块化策略对具有非细胞黏附性质的主链多糖进行修饰。在此基础上,对超分子海绵的物理化学特性进行了研究,结果表明超分子二聚体的存在改善了它们的机械性能并诱导了不同的结构。此外,小角中子散射(SANS)测量和流变学实验表明,UPy-二聚体进入琼脂糖主链能够在变薄的聚集体中重新排列。还证明了表面上的 UPy-琼脂糖(AGA-UPy)基序能够促进细胞黏附。最后,最后一种方法表明,这种新型材料在生物黏附支架中的应用具有巨大的潜力,表明神经干细胞在软材料中表现出扩散偏置,并且与对照(即未修饰的海绵)相比,所有 UPy 修饰的海绵的细胞黏附都得到了增强。因此,通过用 UPy-二聚体功能化海绵表面,构建了一种黏附的超分子支架,为神经组织再生开辟了机会。