Iorio Valentina, Troughton Lee D, Hamill Kevin J
Department of Eye and Vision Science, Institute of Ageing and Chronic Disease, University of Liverpool , Liverpool, United Kingdom .
Adv Wound Care (New Rochelle). 2015 Apr 1;4(4):250-263. doi: 10.1089/wound.2014.0533.
Laminins are complex extracellular macromolecules that are major players in the control of a variety of core cell processes, including regulating rates of cell proliferation, differentiation, adhesion, and migration. Laminins, and related extracellular matrix components, have essential roles in tissue homeostasis; however, during wound healing, the same proteins are critical players in re-epithelialization and angiogenesis. Understanding how these proteins influence cell behavior in these different conditions holds great potential in identifying new strategies to enhance normal wound closure or to treat chronic/nonhealing wounds. Laminin-derived bioactive peptides and, more recently, laminin-peptide conjugated scaffolds, have been designed to improve tissue regeneration after injuries. These peptides have been shown to be effective in decreasing inflammation and granulation tissue, and in promoting re-epithelialization, angiogenesis, and cell migration. Although there is now a wealth of knowledge concerning laminin form and function, there are still areas of some controversy. These include the relative contribution of two laminin-based adhesive devices (focal contacts and hemidesmosomes) to the re-epithelialization process, the impact and implications of laminin proteolytic processing, and the importance of laminin polymer formation on cell behavior. In addition, the roles in wound healing of the laminin-related proteins, netrins, and LaNts are still to be fully defined. The future of laminin-based therapeutics potentially lies in the bioengineering of specific substrates to support laminin deposition for expansion of autologous cells for graft formation and transplantation. Significant recent advances suggest that this goal is within sight.
层粘连蛋白是复杂的细胞外大分子,在多种核心细胞过程的调控中起主要作用,包括调节细胞增殖、分化、黏附和迁移的速率。层粘连蛋白以及相关的细胞外基质成分在组织稳态中具有重要作用;然而,在伤口愈合过程中,这些相同的蛋白质是再上皮化和血管生成的关键参与者。了解这些蛋白质如何在这些不同条件下影响细胞行为,对于确定增强正常伤口闭合或治疗慢性/不愈合伤口的新策略具有巨大潜力。源自层粘连蛋白的生物活性肽,以及最近的层粘连蛋白 - 肽共轭支架,已被设计用于改善损伤后的组织再生。这些肽已被证明在减轻炎症和肉芽组织、促进再上皮化、血管生成和细胞迁移方面有效。尽管现在关于层粘连蛋白的形式和功能有丰富的知识,但仍存在一些有争议的领域。这些包括两种基于层粘连蛋白的黏附装置(黏着斑和半桥粒)对再上皮化过程的相对贡献、层粘连蛋白蛋白水解加工的影响和意义,以及层粘连蛋白聚合物形成对细胞行为的重要性。此外,层粘连蛋白相关蛋白、netrins和LaNts在伤口愈合中的作用仍有待充分确定。基于层粘连蛋白的治疗方法的未来可能在于生物工程设计特定的基质,以支持层粘连蛋白的沉积,用于自体细胞的扩增以形成移植物并进行移植。最近的重大进展表明这一目标已近在眼前。