Type VII Collagen: The Anchoring Fibril Protein at Fault in Dystrophic Epidermolysis Bullosa

被引:129
作者
Chung, Hye Jin
Uitto, Jouni [1 ]
机构
[1] Thomas Jefferson Univ, Jefferson Med Coll, Dept Dermatol & Cutaneous Surg, Philadelphia, PA 19107 USA
关键词
Epidermolysis bullosa; Type VII collagen; Anchoring fibrils; Heritable blistering diseases; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR-BETA; MUTATION ANALYSIS; GENETIC-LINKAGE; EPIDERMAL-KERATINOCYTES; NC1; DOMAIN; HUMAN SKIN; COL7A1; IDENTIFICATION; EXPRESSION;
D O I
10.1016/j.det.2009.10.011
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Type VII collagen is a major component of the anchoring fibrils of the dermal-epidermal adhesion on the dermal side at the lamina densa/papillary dermis interface. Dystrophic epidermolysis bullosa (DEB) emerged as a candidate for type VII collagen mutations becausing anchoring fibrils were shown to be morphologically altered, reduced in number, or completely absent in patients with different forms of DEB. Circulating autoantibodies recognize type VII collagen epitopes in epidermolysis bullosa acquisita. The suggestion that type VII collagen is required for human epidermal tumorigenesis relates to the increasing numbers of life-threatening complications associated with developing squamous cell carcinomas because of the extended life span of affected individuals with recessive DEB.
引用
收藏
页码:93 / +
页数:14
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