Role of keratinocyte–fibroblast cross‐talk in development of hypertrophic scar

伤口愈合 旁分泌信号 细胞外基质 成纤维细胞 细胞生物学 角质形成细胞 增生性瘢痕 自分泌信号 人口 生物 基质金属蛋白酶 免疫学 医学 病理 细胞培养 内科学 受体 遗传学 环境卫生
作者
Aziz Ghahary,Abdi Ghaffari
出处
期刊:Wound Repair and Regeneration [Wiley]
卷期号:15 (s1) 被引量:123
标识
DOI:10.1111/j.1524-475x.2007.00225.x
摘要

The ability to generate or repair injured tissue is essential to the continuity of human life. As in all other organs, wound healing in the skin is a dynamic process involving tissue response to different types of insults. This process involves a continuous sequence of signals and responses in which platelets, fibroblasts, epithelial, endothelial, and immune cells come together outside their usual domains to orchestrate a very complex event that results in tissue repair. These signals, which are mainly growth factors and cytokines, orchestrate the initiation, continuation, and termination of wound healing. An imbalance in the synthesis and release of these cytokines and growth factors at the wound site, therefore, may result in either retarded wound healing, as is seen in diabetic patients and the elderly population, or overhealing wounds such as fibroproliferative disorders frequently seen following surgical incision, traumatic wounds, and severe electrical and thermal injury. In general, regardless of the site of injury, in any phase of the dynamic healing process, a fine balance between synthesis of extracellular matrix and degradation by a large family of enzymes, known as matrix metalloproteinases, is required for maintaining the structural integrity of healing tissue. The availability of new models such as organotypic co-culture systems have allowed us to gain new insight into the cell-cell interactions at both cellular and molecular levels. Recent evidence indicates that mesenchymal-epithelial interactions play a critical role in regulation of skin homeostasis and this cross-talk is mediated by soluble factors acting as autocrine/paracrine regulators of fibroblast and keratinocyte growth, function, and differentiation. In this review we address the question of how keratinocyte-fibroblast interaction plays a role in controlling the expression of key extracellular matrix molecules such as matrix metalloproteinases, which are critical in the healing process following any types of insults to the skin.

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