Aszódi A, Hunziker E B, Olsen B R, Fässler R
Department of Experimental Pathology, Lund University, Sweden.
Osteoarthritis Cartilage. 2001;9 Suppl A:S150-9.
The extracellular matrix (ECM) of hyaline cartilage contains an elaborated collagen fibrillar network, which is essential for the mechanical stability and the proper function of the tissue. Cartilage collagen fibrils consist of collagen II, the quantitatively minor collagens IX and XI, and several non-collagenous fibril-associated proteins. To understand the role some of these molecules in skeletal development, we have generated transgenic mouse strains harboring ablated genes for collagens II and IX, and matrilin-1.
Mice lacking collagen II, collagen IX and matrilin-1 have been established earlier in our laboratory using standard techniques. To determine the consequences of the null mutations we used skeletal staining, histochemical and immunohistochemical assays, in situ hybridization and ultrastructural analysis.
Transgenic mice deficient in collagen II (Col2a1-/-) die at birth and display a severely malformed skeleton characterized by abnormal endochondral ossification and impaired intervertebral disc development. Mice lacking collagen IX (Col9a1-/-) are viable and develop an osteoarthritis-like phenotype in knee joints between 9-12 months of age. To test the possibility that the reduction in collagen II content has an influence on the onset of degenerative changes of articular cartilage, we have generated mice, which are heterozygous for the collagen II null mutation and homozygous for the collagen IX null mutation. Col2a1+/- Col9a1-/- mice show no accelerated development of osteoarthritis compared with the collagen IX knockout animals. Finally, mice lacking matrilin-1, a non-collagenous glycoprotein that binds to both collagen fibrils and aggrecan, develop normally without detectable abnormalities in their skeleton.
Our transgenic mouse strains carrying null mutations in genes encoding cartilage ECM proteins demonstrate that these proteins have different roles during skeletal development. Collagen II is important for cartilage formation, collagen IX for cartilage maintenance and matrilin-1 is redundant.
透明软骨的细胞外基质(ECM)包含一个精细的胶原纤维网络,这对于组织的机械稳定性和正常功能至关重要。软骨胶原纤维由胶原II、数量较少的胶原IX和XI以及几种非胶原性纤维相关蛋白组成。为了了解这些分子中的一些在骨骼发育中的作用,我们构建了携带胶原II和IX以及基质金属蛋白酶-1基因缺失的转基因小鼠品系。
我们实验室先前已使用标准技术建立了缺乏胶原II、胶原IX和基质金属蛋白酶-1的小鼠。为了确定无效突变的后果,我们使用了骨骼染色、组织化学和免疫组织化学分析、原位杂交和超微结构分析。
缺乏胶原II(Col2a1-/-)的转基因小鼠出生时死亡,并表现出严重畸形的骨骼,其特征为软骨内骨化异常和椎间盘发育受损。缺乏胶原IX(Col9a1-/-)的小鼠能够存活,并在9至12个月大时在膝关节出现骨关节炎样表型。为了测试胶原II含量的降低是否会影响关节软骨退变变化的发生,我们构建了胶原II无效突变杂合且胶原IX无效突变纯合的小鼠。与胶原IX基因敲除动物相比,Col2a1+/- Col9a1-/-小鼠未显示骨关节炎加速发展。最后,缺乏基质金属蛋白酶-1(一种与胶原纤维和聚集蛋白聚糖都结合的非胶原糖蛋白)的小鼠发育正常,骨骼未检测到异常。
我们携带软骨ECM蛋白编码基因无效突变的转基因小鼠品系表明,这些蛋白在骨骼发育过程中具有不同作用。胶原II对软骨形成很重要,胶原IX对软骨维持很重要,而基质金属蛋白酶-1是多余的。