Peltonen L, Palotie A, Prockop D J
Proc Natl Acad Sci U S A. 1980 Oct;77(10):6179-83. doi: 10.1073/pnas.77.10.6179.
Fibroblasts from normal human subjects and from a patient who had osteogenesis imperfecta were incubated with [3H]mannose, and types I and III procollagens were isolated from the culture medium. The type I procollagen from the patient's fibroblasts contained 2-3 time more [3H]mannose than the type I procollagen from the normal fibroblasts. In contrast, there was no difference in the [3H]mannose content of the type III procollagen simultaneously synthesized and secreted by the same cells. Isolation of a collagenase-resistant peptide fragment from the type I procollagen showed that the excess mannose was located in the COOH-terminal propeptide of the protein. Radioimmunoassays of the medium and the cell layer showed that the type I procollagen synthesized by the patient's fibroblasts was secreted into the medium more slowly than the type I procollagen synthesized by normal fibroblasts. These results appear to provide evidence for an alteration in the structure of procollagen in osteogenesis imperfecta.
将来自正常人类受试者和成骨不全症患者的成纤维细胞与[3H]甘露糖一起孵育,然后从培养基中分离出I型和III型前胶原。患者成纤维细胞产生的I型前胶原所含的[3H]甘露糖比正常成纤维细胞产生的I型前胶原多2至3倍。相比之下,同一细胞同时合成和分泌的III型前胶原的[3H]甘露糖含量没有差异。从I型前胶原中分离出一种抗胶原酶的肽片段,结果表明多余的甘露糖位于该蛋白质的COOH末端前肽中。对培养基和细胞层进行放射免疫测定表明,患者成纤维细胞合成的I型前胶原分泌到培养基中的速度比正常成纤维细胞合成的I型前胶原慢。这些结果似乎为成骨不全症中前胶原结构的改变提供了证据。