Delvoye P, Mauch C, Krieg T, Lapiere C M
Br J Dermatol. 1986 Aug;115(2):139-46. doi: 10.1111/j.1365-2133.1986.tb05709.x.
Fibroblasts derived from patients and animals presenting various heritable connective tissue disorders were investigated for the ability to retract a reconstituted collagen matrix. When seeded into gels, dermatosparactic calf and sheep fibroblasts did not exhibit the elongated shape of normal fibroblasts and did not contract the collagen lattice to the same extent as control fibroblasts. In contrast, several cell strains obtained from patients with Ehlers-Danlos syndrome type VII displayed contractile properties for collagen gels similar to controls. Delayed contraction was noted by two strains of fibroblasts from patients with Ehlers-Danlos syndrome type IV, whereas fibroblasts from patients with osteogenesis imperfecta, Marfan syndrome and cutis laxa had normal retraction properties.
对来自患有各种遗传性结缔组织疾病的患者和动物的成纤维细胞进行了研究,以检测其使重组胶原基质收缩的能力。当接种到凝胶中时,皮肤松垂症的小牛和绵羊成纤维细胞没有呈现出正常成纤维细胞的细长形状,并且与对照成纤维细胞相比,没有使胶原晶格收缩到相同程度。相比之下,从VII型埃勒斯-当洛综合征患者获得的几种细胞株对胶原凝胶表现出与对照相似的收缩特性。IV型埃勒斯-当洛综合征患者的两株成纤维细胞出现收缩延迟,而来自成骨不全、马凡综合征和皮肤松弛症患者的成纤维细胞具有正常的收缩特性。