Longmate Whitney M, Dipersio C Michael
Center for Cell Biology and Cancer Research, Albany Medical College , Albany, New York.
Adv Wound Care (New Rochelle). 2014 Mar 1;3(3):229-246. doi: 10.1089/wound.2013.0516.
Integrins are bidirectional signaling receptors for extracellular matrix that regulate both inside-out signaling that controls keratinocyte-mediated changes to the wound microenvironment and outside-in signaling that controls keratinocyte responses to microenvironmental changes. As such, integrins represent attractive therapeutic targets for treatment of chronic wounds or general promotion of wound healing. Advances in wound management are particularly important as the elderly and diabetic populations within the United States continue to grow. Although integrins are best known for mediating cell adhesion and migration, integrins in wound epidermis also control cell survival, proliferation, matrix remodeling, and paracrine crosstalk to other cellular compartments of the wound. Importantly, the concept of targeting integrins in the clinic has been established for treatment of certain cancers and other diseases, laying the groundwork for similar exploitation of integrins as targets to treat chronic wounds. Despite their attractiveness as therapeutic targets, integrins have complex roles in wound healing that are impacted by both their own expression and a highly dynamic wound microenvironment that determines ligand availability. Therefore, identifying relevant integrin ligands in the wound and understanding both distinct and overlapping functions that different integrins play in the epidermis will be critical to determine their precise roles in wound healing. Future research should focus on gaining a thorough understanding of the highly coordinated functions of different integrins in wound epidermis, and on determining which of these functions go awry in pathological wounds. This focus should facilitate development of integrin-targeting therapeutics for treating chronic wounds.
整合素是细胞外基质的双向信号受体,可调节控制角质形成细胞介导的伤口微环境变化的由内向外信号传导以及控制角质形成细胞对微环境变化反应的由外向内信号传导。因此,整合素是治疗慢性伤口或普遍促进伤口愈合的有吸引力的治疗靶点。随着美国老年人口和糖尿病患者数量持续增长,伤口管理方面的进展尤为重要。尽管整合素最广为人知的功能是介导细胞黏附和迁移,但伤口表皮中的整合素还控制细胞存活、增殖、基质重塑以及与伤口其他细胞区室的旁分泌相互作用。重要的是,针对某些癌症和其他疾病的临床治疗中靶向整合素的概念已经确立,为将整合素作为治疗慢性伤口的靶点进行类似开发奠定了基础。尽管整合素作为治疗靶点具有吸引力,但它们在伤口愈合中具有复杂的作用,这既受到其自身表达的影响,也受到决定配体可用性的高度动态的伤口微环境的影响。因此,确定伤口中相关的整合素配体,并了解不同整合素在表皮中发挥的独特和重叠功能,对于确定它们在伤口愈合中的精确作用至关重要。未来的研究应专注于深入了解伤口表皮中不同整合素的高度协调功能,并确定哪些功能在病理性伤口中出现异常。这种关注应有助于开发用于治疗慢性伤口的整合素靶向疗法。