Chen Q A, Gibney E, Fitch J M, Linsenmayer C, Schmid T M, Linsenmayer T F
Department of Anatomy and Cellular Biology, Tufts University Health Science Schools, Boston, MA 02111.
Proc Natl Acad Sci U S A. 1990 Oct;87(20):8046-50. doi: 10.1073/pnas.87.20.8046.
A recent immunoelectron microscopic study of type X collagen in developing cartilage gave results that could be explained by movement of the molecule from one region of the cartilage matrix to another, there becoming associated with preexisting collagen fibrils. In the present study, to test the feasibility of this model we incubated pieces of nonhypertrophic, embryonic chicken sternal cartilage (which has no endogenous type X collagen) in medium with type X collagen and then used immunofluorescence and immunoelectron microscopy to evaluate movement of the molecule through the matrix. The results show that type X collagen molecules can indeed pass through embryonic sternal cartilage matrix and subsequently become fibril-associated.
最近一项关于发育中软骨组织中X型胶原蛋白的免疫电子显微镜研究结果表明,该分子可从软骨基质的一个区域移动到另一个区域,并与预先存在的胶原纤维相结合。在本研究中,为了验证该模型的可行性,我们将未肥大的胚胎鸡胸骨软骨片(其不含内源性X型胶原蛋白)置于含有X型胶原蛋白的培养基中进行孵育,然后利用免疫荧光和免疫电子显微镜技术评估该分子在基质中的移动情况。结果显示,X型胶原蛋白分子确实能够穿过胚胎胸骨软骨基质,并随后与纤维相结合。