Premature Collagen Fibril Formation, Fibroblast-Mast Cell Interactions and Mast Cell-Mediated Phagocytosis of Collagen in Keloids

被引:29
作者
Arbi, Sandra [1 ]
Eksteen, Ehren Cronje [2 ]
Oberholzer, Hester Magdalena [1 ]
Taute, Helena [1 ]
Bester, Megan Jean [1 ]
机构
[1] Univ Pretoria, Fac Hlth Sci, Dept Anat, ZA-0007 Pretoria, South Africa
[2] Univ Pretoria, Steve Biko Acad Hosp, Div Plast Surg, ZA-0007 Pretoria, South Africa
基金
新加坡国家研究基金会;
关键词
Collagen; fiber; fibroblast; intracellular; keloid; mast cell; FIBROSIS; PATHOGENESIS; ULTRASTRUCTURE; EXPRESSION; MOLECULES; LUNG; BETA;
D O I
10.3109/01913123.2014.981326
中图分类号
TH742 [显微镜];
学科分类号
080401 [精密仪器及机械];
摘要
Keloids are benign hyper-proliferative growths of fibrous tissue where increased fibroblast activity results in abnormal collagen deposition. Excessive inflammation is a characteristic feature of keloids, but little is known about the underlying ultrastructural features of keloids related to collagen processing, fibril and fiber formation, the interaction between fibroblasts and associated collagen fibers and mast cells. In this study, the ultrastructure of the dermis of keloid patients was evaluated using light and transmission electron microscopy techniques. Abnormal intracellular premature collagen fibril formation was observed. Phagocytosis of collagen fibrils by mast cells was a common ultrastructural feature of keloid tissue as was a close or direct association between fibroblasts and mast cells. Based on these findings and recent advances in knowledge related to collagen synthesis, fibril formation and processing, we hypothesize that keloid formation is primarily due to abnormal collagen synthesis where the consequent accumulation of collagen fibers causes increased mast cell recruitment and collagen phagocytosis. Subsequent release of mast cell-derived mediators then promotes further collagen synthesis. The observation of early formation in keloid tissue of premature insoluble collagen fibrils supports previous studies that enzymes such as procollagen C-proteinase are important early therapeutic targets.
引用
收藏
页码:95 / 103
页数:9
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