A Review of the Contribution of Mast Cells in Wound Healing: Involved Molecular and Cellular Mechanisms

伤口愈合 血管内皮生长因子 细胞生物学 成纤维细胞生长因子 干细胞因子 成纤维细胞 生长因子 血小板衍生生长因子 真皮 血管生成 血小板源性生长因子受体 皮肤修复 碱性成纤维细胞生长因子 生物 促炎细胞因子 炎症 免疫学 细胞外基质 干细胞 癌症研究 医学 病理 祖细胞 内科学 细胞培养 受体 血管内皮生长因子受体 遗传学
作者
Daniel Elieh Ali Komi,Kelly Khomtchouk,Peter L. Santa Maria
出处
期刊:Clinical Reviews in Allergy & Immunology [Springer Nature]
卷期号:58 (3): 298-312 被引量:373
标识
DOI:10.1007/s12016-019-08729-w
摘要

Mast cells (MCs), apart from their classic role in allergy, contribute to a number of biologic processes including wound healing. In particular, two aspects of their histologic distribution within the skin have attracted the attention of researchers to study their wound healing role; they represent up to 8% of the total number of cells within the dermis and their cutaneous versions are localized adjacent to the epidermis and the subdermal vasculature and nerves. At the onset of a cutaneous injury, the accumulation of MCs and release of proinflammatory and immunomodulatory mediators have been well documented. The role of MC-derived mediators has been investigated through the stages of wound healing including inflammation, proliferation, and remodeling. They contribute to hemostasis and clot formation by enhancing the expression of factor XIIIa in dermal dendrocytes through release of TNF-α, and contribute to clot stabilization. Keratinocytes, by secreting stem cell factor (SCF), recruit MCs to the site. MCs in return release inflammatory mediators, including predominantly histamine, VEGF, interleukin (IL)-6, and IL-8, that contribute to increase of endothelial permeability and vasodilation, and facilitate migration of inflammatory cells, mainly monocytes and neutrophils to the site of injury. MCs are capable of activating the fibroblasts and keratinocytes, the predominant cells involved in wound healing. MCs stimulate fibroblast proliferation during the proliferative phase via IL-4, vascular endothelial growth factor (VEGF), and basic fibroblast growth factor (bFGF) to produce a new extracellular matrix (ECM). MC-derived mediators including fibroblast growth factor-2, VEGF, platelet-derived growth factor (PDGF), TGF-β, nerve growth factor (NGF), IL-4, and IL-8 contribute to neoangiogenesis, fibrinogenesis, or reepithelialization during the repair process. MC activation inhibition and targeting the MC-derived mediators are potential therapeutic strategies to improve wound healing through reduced inflammatory responses and scar formation.
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