Piérard G E, Lapière M
J Invest Dermatol. 1976 Jan;66(1):2-7. doi: 10.1111/1523-1747.ep12477969.
Dermatosparaxis is a heritable disorder of the connective tissue observed in the calf and is related to the presence in the dermis of a form of procollagen, rather than collagen, forming the fibrous support of the skin. This alteration results from the lack of activity of procollagen peptidase, an enzyme required for the final processing of procollagen in collagen. Skin in dermatosparaxis displays abnormal mechanical properties. Procollagen forms poorly structured fibers loosely packed in sheets and dispersed within an excess of glycosaminoglycans. This disturbed architectural organization is responsible for the hyperextensibility and poor elasticity of the dermatosparactic dermis. Skin fragility is related to the impaired mechanical properties of the procollagen polymers. Rupture occurs in the mid-dermis in a location where the connective tissue is devoid of adnexae and elastic fibers.
皮肤松垂症是一种在小牛身上观察到的遗传性结缔组织疾病,它与真皮中一种形成皮肤纤维支撑的前胶原蛋白(而非胶原蛋白)的存在有关。这种改变是由于前胶原蛋白肽酶缺乏活性所致,前胶原蛋白肽酶是胶原蛋白中前胶原蛋白最终加工所需的一种酶。皮肤松垂症患者的皮肤表现出异常的机械性能。前胶原蛋白形成结构不良的纤维,这些纤维松散地堆积成片,并分散在过量的糖胺聚糖中。这种紊乱的结构组织导致了皮肤松垂症患者真皮的过度伸展性和弹性差。皮肤脆弱性与前胶原蛋白聚合物受损的机械性能有关。破裂发生在真皮中部,此处结缔组织缺乏附属器和弹性纤维。