Department of Bioengineering and iBB - Institute of Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001, Lisbon, Portugal.
Department of Chemistry and Chemical Biology, Biological Sciences and Chemical and Biological Engineering, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY, 12180-3590, USA.
Glycoconj J. 2019 Apr;36(2):141-154. doi: 10.1007/s10719-019-09858-2. Epub 2019 Jan 14.
The extracellular matrix (ECM) is a highly dynamic and complex meshwork of proteins and glycosaminoglycans (GAGs) with a crucial role in tissue homeostasis and organization not only by defining tissue architecture and mechanical properties, but also by providing chemical cues that regulate major biological processes. GAGs are associated with important physiological functions, acting as modulators of signaling pathways regulating several cellular processes such as cell growth and differentiation. Recently, in vitro fabricated cell-derived ECM have emerged as promising materials for regenerative medicine due to their ability of better recapitulate the native ECM-like composition and structure, without the limitations of availability and pathogen transfer risks of tissue-derived ECM scaffolds. However, little is known about the molecular and more specifically, GAG composition of these cell-derived ECM. In this study, three different cell-derived ECM were produced in vitro and characterized in terms of their GAG content, composition and sulfation patterns using a highly sensitive liquid chromatography-tandem mass spectrometry technique. Distinct GAG compositions and disaccharide sulfation patterns were verified for the different cell-derived ECM. Additionally, the effect of decellularization method on the GAG and disaccharide relative composition was also assessed. In summary, the method presented here offers a novel approach to determine the GAG composition of cell-derived ECM, which we believe is critical for a better understanding of ECM role in directing cellular responses and has the potential for generating important knowledge to use in the development of novel ECM-like biomaterials for tissue engineering applications.
细胞外基质(ECM)是一种高度动态和复杂的蛋白质和糖胺聚糖(GAG)网格,对于组织稳态和组织具有至关重要的作用,不仅通过定义组织架构和机械性能,还通过提供化学线索来调节主要的生物学过程。GAG 与重要的生理功能相关,作为调节细胞生长和分化等多种细胞过程的信号通路调节剂。最近,由于其更好地再现天然 ECM 样组成和结构的能力,而没有组织衍生的 ECM 支架的可用性和病原体转移风险的限制,体外制造的细胞衍生 ECM 已成为再生医学中很有前途的材料。然而,对于这些细胞衍生的 ECM 的分子特性,特别是 GAG 组成,知之甚少。在这项研究中,使用高度灵敏的液相色谱-串联质谱技术,在体外产生了三种不同的细胞衍生 ECM,并从 GAG 含量、组成和磺化模式方面对其进行了表征。证实了不同细胞衍生 ECM 的不同 GAG 组成和二糖磺化模式。此外,还评估了脱细胞方法对 GAG 和二糖相对组成的影响。总之,这里提出的方法提供了一种确定细胞衍生 ECM 的 GAG 组成的新方法,我们认为这对于更好地理解 ECM 在指导细胞反应中的作用至关重要,并有可能为开发用于组织工程应用的新型 ECM 样生物材料提供重要知识。