Department of Ophthalmology, Boston University School of Medicine, Boston, MA, USA.
J Cell Physiol. 2013 May;228(5):925-9. doi: 10.1002/jcp.24268.
Epithelial wounds usually heal relatively quickly, but repair may be impaired by environmental stressors, such as hypoxic or diabetic states, rendering patients vulnerable to a number of corneal pathologies. Though this response appears simple, at first, years of research have uncovered the complicated biochemical pathways coordinating the wound healing response. Here, we investigate signaling cascades and individual proteins involved in the corneal epithelium's self-repair. We will explore how an epithelial cell migrates across the wound bed and attaches itself to its new post-injury surroundings, including its neighboring cells and the basement membrane, through focal adhesions and hemidesmosomes. We will also discuss how the cell coordinates this motion physiologically, through calcium signaling and protein phosphorylation, focusing on the communication through purinergic, glutamatergic, and growth factor receptors. Many of these aspects reflect and can be extended to similar epithelial surfaces, and can be used to facilitate wound healing in patients with various underlying pathologies. The collective library of laboratory and clinical research done around the world has demonstrated how important precise regulation of these processes is in order for the injured corneal epithelium to properly heal.
上皮组织的创伤通常能较快愈合,但修复可能会受到环境应激源的影响,如缺氧或糖尿病状态,使患者易患多种角膜病变。尽管这种反应看似简单,但经过多年的研究,人们已经揭示了协调创伤愈合反应的复杂生化途径。在这里,我们研究了角膜上皮自我修复过程中涉及的信号级联和单个蛋白。我们将探讨上皮细胞如何通过粘着斑和半桥粒穿过创伤床并附着在新的损伤后环境上,包括其邻近细胞和基底膜。我们还将讨论细胞如何通过钙信号和蛋白磷酸化来协调这种运动,并重点关注嘌呤能、谷氨酸能和生长因子受体的通讯。这些方面中的许多反映了并可扩展到类似的上皮表面,并可用于促进各种潜在病理患者的伤口愈合。世界各地进行的实验室和临床研究的综合研究表明,为了使受伤的角膜上皮组织能正常愈合,精确调节这些过程是多么重要。