Native human collagen type I provides a viable physiologically relevant alternative to xenogeneic sources for tissue engineering applications: A comparative in vitro and in vivo study.
Tânia Baltazar, Nilabh S Kajave, Marco Rodriguez, Srija Chakraborty, Bo Jiang, Aleksander Skardal, Vipuil Kishore, Jordan S Pober, Mohammad Z Albanna
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引用次数: 0
Abstract
Xenogeneic sources of collagen type I remain a common choice for regenerative medicine applications due to ease of availability. Human and animal sources have some similarities, but small variations in amino acid composition can influence the physical properties of collagen, cellular response, and tissue remodeling. The goal of this work is to compare human collagen type I-based hydrogels versus animal-derived collagen type I-based hydrogels, generated from commercially available products, for their physico-chemical properties and for tissue engineering and regenerative medicine applications. Specifically, we evaluated whether the native human skin type I collagen could be used in the three most common research applications of this protein: as a substrate for attachment and proliferation of conventional 2D cell culture; as a source of matrix for a 3D cell culture; and as a source of matrix for tissue engineering. Results showed that species and tissue specific variations of collagen sources significantly impact the physical, chemical, and biological properties of collagen hydrogels including gelation kinetics, swelling ratio, collagen fiber morphology, compressive modulus, stability, and metabolic activity of hMSCs. Tumor constructs formulated with human skin collagen showed a differential response to chemotherapy agents compared to rat tail collagen. Human skin collagen performed comparably to rat tail collagen and enabled assembly of perfused human vessels in vivo. Despite differences in collagen manufacturing methods and supplied forms, the results suggest that commercially available human collagen can be used in lieu of xenogeneic sources to create functional scaffolds, but not all sources of human collagen behave similarly. These factors must be considered in the development of 3D tissues for drug screening and regenerative medicine applications.
原生人类 I 型胶原蛋白为组织工程应用提供了一种可行的、与生理相关的异种来源替代品:体外和体内比较研究。
异种来源的 I 型胶原蛋白由于易于获得,仍然是再生医学应用的常见选择。人源和动物源有一些相似之处,但氨基酸组成的微小差异会影响胶原蛋白的物理性质、细胞反应和组织重塑。这项研究的目的是比较人类 I 型胶原蛋白水凝胶与动物来源的 I 型胶原蛋白水凝胶(由市售产品制成)的物理化学特性以及在组织工程和再生医学应用中的效果。具体来说,我们评估了原生人体皮肤 I 型胶原蛋白是否可用于该蛋白质最常见的三种研究应用:作为传统二维细胞培养的附着和增殖基质;作为三维细胞培养的基质来源;以及作为组织工程的基质来源。研究结果表明,胶原蛋白来源的物种和组织特异性变化会显著影响胶原蛋白水凝胶的物理、化学和生物特性,包括凝胶化动力学、膨胀率、胶原纤维形态、压缩模量、稳定性和 hMSCs 的代谢活性。与大鼠尾部胶原蛋白相比,用人皮胶原蛋白配制的肿瘤组织对化疗药物的反应不同。人皮胶原蛋白的性能与鼠尾胶原蛋白相当,并能在体内组装灌注人血管。尽管胶原蛋白的制造方法和供应形式存在差异,但研究结果表明,市售的人类胶原蛋白可以代替异种来源的胶原蛋白来制造功能性支架,但并非所有来源的人类胶原蛋白都有类似的表现。在开发用于药物筛选和再生医学应用的三维组织时,必须考虑这些因素。