Aikawa T, Shirasuna K, Iwamoto M, Watatani K, Nakamura T, Okura M, Yoshioka H, Matsuya T
First Department of Oral and Maxillofacial Surgery, Osaka University Faculty of Dentistry, Japan.
J Bone Miner Res. 1996 Apr;11(4):544-53. doi: 10.1002/jbmr.5650110416.
A clonal cell line named RMD-1 was established from the skeletal muscle of a 20-day fetal rat. RMD-1 represents a morphologically homogeneous population of undifferentiated mesenchymal cells, expressing alpha-smooth muscle actin and type I collagen, but no cartilage-associated genes. When cultured in agarose gel containing 100 ng/ml of recombinant human bone morphogenetic protein 2 (rhBMP-2; BMP-2), RMD-1 cells formed colonies and showed chondrocyte-like features as assessed by their ultrastructure, metachromatic staining with toluidine blue, and the production of large hydrodynamic-size proteoglycans. RMD-1 cells also differentiated into chondrocytes when the cells were plated at high density (over 2.5 x 10(5) cells/cm2) on type I collagen and incubated in medium containing 0.5% fetal bovine serum and 100 ng/ml of BMP-2. This chondrogenic differentiation was evidenced by a distinct morphological change into spherical cells, an increase in the levels of sulfated glycosaminoglycans, a decrease in type I collagen mRNA and the expression of cartilage-associated genes, including type II collagen, type IX collagen, aggrecan and alkaline phosphatase. In the presence of ascorbic acid and 10% serum, RMD-1 cells increased in size and expressed type X collagen as well as high alkaline phosphatase activity, then induced matrix mineralization. Thus, RMD-1 is a unique cell line that can differentiate from undifferentiated mesenchymal cells into hypertrophic chondrocytes.
从一只20天大的胎鼠骨骼肌中建立了一个名为RMD-1的克隆细胞系。RMD-1代表了形态学上均一的未分化间充质细胞群体,表达α-平滑肌肌动蛋白和I型胶原蛋白,但不表达与软骨相关的基因。当在含有100 ng/ml重组人骨形态发生蛋白2(rhBMP-2;BMP-2)的琼脂糖凝胶中培养时,RMD-1细胞形成集落,并通过超微结构、甲苯胺蓝异染性染色以及产生大流体动力学尺寸的蛋白聚糖表现出软骨样特征。当将RMD-1细胞以高密度(超过2.5×10⁵个细胞/cm²)接种在I型胶原蛋白上,并在含有0.5%胎牛血清和100 ng/ml BMP-2的培养基中孵育时,它们也会分化为软骨细胞。这种软骨形成分化表现为明显转变为球形细胞的形态变化、硫酸化糖胺聚糖水平的增加、I型胶原蛋白mRNA水平的降低以及包括II型胶原蛋白、IX型胶原蛋白、聚集蛋白聚糖和碱性磷酸酶在内的软骨相关基因的表达。在存在抗坏血酸和10%血清的情况下,RMD-1细胞体积增大,表达X型胶原蛋白以及高碱性磷酸酶活性,随后诱导基质矿化。因此,RMD-1是一种独特的细胞系,能够从未分化的间充质细胞分化为肥大软骨细胞。