Ishizeki K, Hiraki Y, Kubo M, Nawa T
Department of Oral Anatomy, School of Dentistry, Iwate Medical University, Morioka, Japan.
Int J Dev Biol. 1997 Feb;41(1):83-9.
Meckel's cartilage cells cultured in vitro undergo phenotypic transformation toward osteogenic cells. We examined whether these cells synthesize type X collagen and bone morphogenetic protein-2 (BMP-2). We also examined the results of Alcian blue staining and the expression of type I and type II collagen, osteocalcin and chondroitin sulfate proteoglycan (CSPG) during this transdifferentiation. Meckel's chondrocytes, isolated from day-17 mouse embryos, were inoculated at 1 x 10(4)/penicylinder and cultured in alpha-MEM for periods up to 4 weeks. Alcian blue staining and immunostaining of type II collagen and CSPG confirmed that, after cell culture for 2 weeks, the cartilaginous phenotype was expressed most intensely. Later in culture, chondrocytes underwent modification through the synthesis of bone-type proteins; nodule-forming small round cells showed ALPase activity and were immunoreactive for type I collagen and osteocalcin. Immunoreactivity for type X collagen was detected in the small round cells at the top of the nodules prior to calcification of the matrix, as well as in large hypertrophic cells. BMP-2 was also expressed first in similar small round cells after 3 weeks in culture, and it subsequently extended along the extracellular matrix in the calcified nodules. These results indicate that small round cells that are differentiating toward osteocyte-like cells from Meckel's chondrocytes express type X collagen and BMP-2 sequentially.
体外培养的梅克尔软骨细胞会向成骨细胞发生表型转化。我们研究了这些细胞是否合成X型胶原蛋白和骨形态发生蛋白-2(BMP-2)。我们还研究了在此转分化过程中阿尔新蓝染色的结果以及I型和II型胶原蛋白、骨钙素和硫酸软骨素蛋白聚糖(CSPG)的表达情况。从第17天的小鼠胚胎中分离出的梅克尔软骨细胞,以1×10⁴/培养瓶接种,在α-MEM中培养长达4周。阿尔新蓝染色以及II型胶原蛋白和CSPG的免疫染色证实,细胞培养2周后,软骨表型表达最为强烈。在培养后期,软骨细胞通过合成骨型蛋白发生改变;形成结节的小圆形细胞显示出碱性磷酸酶活性,并且对I型胶原蛋白和骨钙素具有免疫反应性。在基质钙化之前,在结节顶部的小圆形细胞以及大的肥大细胞中检测到X型胶原蛋白的免疫反应性。培养3周后,BMP-2也首先在类似的小圆形细胞中表达,随后沿钙化结节中的细胞外基质扩展。这些结果表明,从梅克尔软骨细胞向骨细胞样细胞分化的小圆形细胞依次表达X型胶原蛋白和BMP-2。