Institute of Pharmaceutical Technologies, Lithuanian University of Health Sciences, Sukilėlių ave. 13, LT50162 Kaunas, Lithuania.
Neuroscience Institute, Lithuanian University of Health Sciences, Eivenių str. 4, LT-50161 Kaunas, Lithuania.
Biomolecules. 2020 May 12;10(5):754. doi: 10.3390/biom10050754.
Hydrogel-supported neural cell cultures are more in vivo-relevant compared to monolayers formed on glass or plastic substrates. However, there is a lack of synthetic microenvironment available for obtaining standardized and easily reproducible cultures characterized by tissue-mimicking cell composition, cell-cell interactions, and functional networks. Synthetic peptides representing the biological properties of the extracellular matrix (ECM) proteins have been reported to promote the adhesion-driven differentiation and functional maturation of neural cells. Thus, such peptides can serve as building blocks for engineering a standardized, all-synthetic environment. In this study, we have compared the effect of two chemically crosslinked hydrogel compositions on primary cerebellar cells: collagen-like peptide (CLP), and CLP with an integrin-binding motif arginine-glycine-aspartate (CLP-RGD), both conjugated to polyethylene glycol molecular templates (PEG-CLP and PEG-CLP-RGD, respectively) and fabricated as self-supporting membranes. Both compositions promoted a spontaneous organization of primary cerebellar cells into tissue-like clusters with fast-rising Ca signals in soma, reflecting action potential generation. Notably, neurons on PEG-CLP-RGD had more neurites and better synaptic efficiency compared to PEG-CLP. For comparison, poly-L-lysine-coated glass and plastic surfaces did not induce formation of such spontaneously active networks. Additionally, contrary to the hydrogel membranes, glass substrates functionalized with PEG-CLP and PEG-CLP-RGD did not sufficiently support cell attachment and, subsequently, did not promote functional cluster formation. These results indicate that not only chemical composition but also the hydrogel structure and viscoelasticity are essential for bioactive signaling. The synthetic strategy based on ECM-mimicking, multifunctional blocks in registry with chemical crosslinking for obtaining tissue-like mechanical properties is promising for the development of fast and well standardized functional in vitro neural models and new regenerative therapies.
水凝胶支持的神经细胞培养物比在玻璃或塑料基底上形成的单层更接近体内环境。然而,缺乏用于获得具有组织模拟细胞组成、细胞间相互作用和功能网络的标准化和可重复培养物的合成微环境。已报道,代表细胞外基质(ECM)蛋白生物特性的合成肽可促进神经细胞的粘附驱动分化和功能成熟。因此,这些肽可以作为构建块来设计标准化的全合成环境。在这项研究中,我们比较了两种化学交联水凝胶成分对原代小脑细胞的影响:胶原样肽(CLP)和含有整合素结合基序精氨酸-甘氨酸-天冬氨酸(CLP-RGD)的 CLP,两者均与聚乙二醇分子模板(PEG-CLP 和 PEG-CLP-RGD)共轭,并制成自支撑膜。这两种成分都促进了原代小脑细胞自发组织化为具有快速上升的胞体钙信号的类组织簇,反映了动作电位的产生。值得注意的是,与 PEG-CLP 相比,PEG-CLP-RGD 上的神经元具有更多的神经突和更好的突触效率。相比之下,聚-L-赖氨酸涂覆的玻璃和塑料表面不会诱导形成这种自发活跃的网络。此外,与水凝胶膜不同,用 PEG-CLP 和 PEG-CLP-RGD 功能化的玻璃底物不能充分支持细胞附着,随后也不能促进功能簇的形成。这些结果表明,不仅化学组成,而且水凝胶结构和粘弹性对于生物活性信号至关重要。基于与化学交联 registry 的 ECM 模拟、多功能块的合成策略,用于获得类组织机械性能,有望开发快速且标准化良好的体外神经功能模型和新的再生治疗方法。