Department of Cell Biology, Genetics and Physiology, Faculty of Science, University of Malaga, IBIMA, Malaga, Spain; Materials Science Institute of Seville (ICMS), Joint CSIC-University of Seville Center, Seville, Spain; Andalusian Center for Nanomedicine and Biotechnology (BIONAND), Malaga, Spain; Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Spain.
Department of Cell Biology, Genetics and Physiology, Faculty of Science, University of Malaga, IBIMA, Malaga, Spain; Andalusian Center for Nanomedicine and Biotechnology (BIONAND), Malaga, Spain; Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Spain.
Mater Sci Eng C Mater Biol Appl. 2021 Jan;120:111679. doi: 10.1016/j.msec.2020.111679. Epub 2020 Oct 27.
Fibrous biopolymeric collagen extracted from animal tissues has been widely used for fabricating matrices for bone tissue engineering (BTE). However, animal extracted collagens can trigger immune reactions when implanted in vivo and the presence of native crosslinks leads to batch-to-batch variability. Atelocollagen, a monomeric form of collagen, is free of telopeptides, which are mainly responsible for the immunogenicity of collagen, and can self-assemble in vitro to obtain fibrils with the characteristic D-periodic staining pattern of native collagen. However, atelocollagen-based biomaterials have not extensively been studied and, hence, their suitability for BTE remains relatively unexplored. Besides, to stabilize collagen biomaterials, chemical and physical crosslinking are used, although chemical agents are cytotoxic while the physical methods yield a less effective crosslinking. A combination of physical and chemical crosslinking is a suitable alternative that has rarely been tested in BTE programs. In this work, a sponge-like biomaterial (DCol-S) was processed from D-periodic self-assembled atelocollagen and its stabilization was studied using the combination of a dehydrothermal treatment (DHT) and minimal glutaraldehyde (GTA) exposition crosslinking, to increase the resistance to degradation of the scaffold without a major effect on the biomaterial structure. The microstructural features of the final sponges were characterised and compared to a commercial biomaterial processed from native bovine collagen (Helistat®, Integra Lifesciences, NJ, USA), demonstrating that a D-periodic nanostructure was obtained and maintained after processing of the sponges. MC3T3-E1 preosteoblast adhesion, proliferation and differentiation assays in vitro showed that DCol-S is biocompatible. Furthermore, intramuscular implantation of the biomaterials loaded with rhBMP-2 revealed that the double-crosslinked sponges were able to support ectopic bone formation, while sponges stabilised only with the DHT treatment were not. Altogether, these findings show that atelocollagen-based sponges stabilised with a DHT treatment followed by a mild GTA crosslinking are a suitable alternative to polymeric extracted collagen for BTE applications.
从动物组织中提取的纤维状生物聚合物胶原已广泛用于制造骨组织工程(BTE)的基质。然而,当植入体内时,动物提取的胶原蛋白会引发免疫反应,并且天然交联的存在导致批次间的可变性。atelocollagen 是胶原蛋白的单体形式,没有 telopeptides,telopeptides 主要负责胶原蛋白的免疫原性,并且可以在体外自组装以获得具有天然胶原蛋白特征 D 周期染色图案的原纤维。然而,基于 atelocollagen 的生物材料尚未广泛研究,因此其在 BTE 中的适用性仍相对未知。此外,为了稳定胶原蛋白生物材料,使用化学和物理交联,尽管化学试剂具有细胞毒性,而物理方法产生的交联效果较差。物理和化学交联的组合是一种合适的替代方法,在 BTE 计划中很少进行测试。在这项工作中,从 D 周期自组装的 atelocollagen 加工了一种海绵状生物材料(DCol-S),并通过结合脱氢热处理(DHT)和最小戊二醛(GTA)暴露交联来研究其稳定性,以提高支架的降解抗性,而对生物材料结构的影响不大。对最终海绵的微观结构特征进行了表征,并与从天然牛胶原蛋白(美国新泽西州 Integra Lifesciences 的 Helistat®)加工而成的商业生物材料进行了比较,证明在加工海绵后获得并保持了 D 周期纳米结构。MC3T3-E1 前成骨细胞黏附、增殖和分化的体外实验表明,DCol-S 具有生物相容性。此外,rhBMP-2 负载的生物材料的肌肉内植入表明,双交联海绵能够支持异位骨形成,而仅用 DHT 处理稳定的海绵则不能。总之,这些发现表明,用 DHT 处理后再用温和的 GTA 交联稳定的 atelocollagen 基海绵是用于 BTE 应用的聚合物提取胶原蛋白的合适替代品。