Cetta G, Rossi A, Tenni R, Valli M, Forlino A, Zanaboni G, Dyne K, Burgio G R
Dipartimento di Biochimica, Università di Pavia, Italy.
Connect Tissue Res. 1993;29(1):41-9. doi: 10.3109/03008209309061965.
To study how mutant type I collagen interferes with matrix deposition we investigated the extracellular matrix produced by cultured skin fibroblasts in thirteen patients affected by different forms of Osteogenesis Imperfecta. Two different approaches were used: a) the pericellular matrix produced during 24 h label was analyzed by SDS-PAGE; b) type I collagen present in the insoluble cell-layer fraction in long-term cultures was studied. Results showed that a very small amount of abnormal type I trimers were present regardless of the clinical phenotype. In only two cases mutant chains were clearly incorporated. These data indicate a selective deposition of normal collagen trimers over abnormal ones. Moreover, in long-term cultures a decreased amount of type I collagen was deposited as indicated by the relative increase in type V collagen. These data are discussed in light of results found in bone by other authors and suggest that decreased deposition of type I collagen could be a general feature in OI and not limited to null-allele OI probands.
为研究突变型I型胶原如何干扰基质沉积,我们调查了13例患有不同形式成骨不全症患者的培养皮肤成纤维细胞产生的细胞外基质。采用了两种不同的方法:a)通过SDS-PAGE分析24小时标记期间产生的细胞周基质;b)研究长期培养中不溶性细胞层部分中存在的I型胶原。结果显示,无论临床表型如何,都存在极少量异常的I型三聚体。仅在两例中,突变链被明确掺入。这些数据表明正常胶原三聚体比异常三聚体有选择性的沉积。此外,在长期培养中,如V型胶原相对增加所示,I型胶原的沉积量减少。根据其他作者在骨骼中发现的结果对这些数据进行了讨论,并表明I型胶原沉积减少可能是成骨不全症的一个普遍特征,而不仅限于无效等位基因成骨不全症先证者。