Institute of Nano Science and Technology (INST), Sector 81, Knowledge City, Mohali, Punjab 140306, India.
ACS Biomater Sci Eng. 2023 Mar 13;9(3):1422-1436. doi: 10.1021/acsbiomaterials.3c00014. Epub 2023 Feb 24.
It has been increasingly evident over the last few years that bioactive peptide hydrogels in conjugation with polymer hydrogels are emerging as a new class of supramolecular materials suitable for various biomedical applications owing to their specificity, tunability, and nontoxicity toward the biological system. Despite their unique biocompatible features, both polymer- and peptide-based scaffolds suffer from certain limitations, which restrict their use toward developing efficient matrices for controlling cellular behavior. The peptide hydrogels usually form soft matrices with low mechanical strength, whereas most of the polymer hydrogels lack biofunctionality. In this direction, combining polymers with peptides to develop a conjugate hydrogel can be explored as an emergent approach to overcome the limitations of the individual components. The polymer will provide high mechanical strength, whereas the biofunctionality of the material can be induced by the bioactive peptide sequence. In this study, we utilized TEMPO-oxidized nanofibrillar cellulose as the polymer counterpart, which was co-assembled with a short N-cadherin mimetic bioactive peptide sequence, Nap-HAVDI, to fabricate an NFC-peptide conjugate hydrogel. Interestingly, the mechanical strength of the peptide hydrogel was found to be significantly improved by combining the peptide with the NFC in the conjugate hydrogel. The addition of the peptide into the NFC also reduced the pore size within NFC matrices, which further helped in improving cellular adhesion, survival, and proliferation. Furthermore, the cells grown on the NFC and NFC-peptide hybrid hydrogel demonstrated normal expression of cytoskeleton proteins, i.e., β-tubulin in C6 cells and actin in L929 cells, respectively. The selective response of neuronal cells toward the specific bioactive peptide was further observed through a protein expression study. Thus, our study demonstrated the collective role of the cellulose-peptide composite material that revealed superior physical properties and biological response of this composite scaffold, which may open up a new platform for biomedical applications.
在过去的几年中,越来越明显的是,由于其特异性、可调节性和对生物系统的非毒性,生物活性肽水凝胶与聚合物水凝胶结合正在成为一类新的超分子材料,适合各种生物医学应用。尽管它们具有独特的生物相容性特征,但基于聚合物和肽的支架都存在某些限制,这限制了它们在开发用于控制细胞行为的有效基质方面的应用。肽水凝胶通常形成机械强度低的软基质,而大多数聚合物水凝胶缺乏生物功能性。在这个方向上,将聚合物与肽结合开发共轭水凝胶可以作为一种新的方法来克服单个成分的限制。聚合物将提供高机械强度,而材料的生物功能性可以通过生物活性肽序列来诱导。在这项研究中,我们利用 TEMPO 氧化的纳米原纤维纤维素作为聚合物对应物,与短的 N-钙粘蛋白模拟生物活性肽序列 Nap-HAVDI 共组装,制备 NFC-肽共轭水凝胶。有趣的是,通过将肽与共轭水凝胶中的 NFC 结合,发现肽水凝胶的机械强度显著提高。肽的加入也减少了 NFC 基质内的孔径,这进一步有助于改善细胞黏附、存活和增殖。此外,在 NFC 和 NFC-肽混合水凝胶上生长的细胞分别表现出正常的细胞骨架蛋白表达,即 C6 细胞中的 β-微管蛋白和 L929 细胞中的肌动蛋白。通过蛋白质表达研究进一步观察到神经元细胞对特定生物活性肽的选择性反应。因此,我们的研究表明纤维素-肽复合材料的协同作用揭示了这种复合材料支架的优异物理性质和生物响应,这可能为生物医学应用开辟一个新的平台。