Enomoto-Iwamoto M, Enomoto H, Komori T, Iwamoto M
Department of Biochemistry, Osaka University Faculty of Dentistry, Japan.
Osteoarthritis Cartilage. 2001;9 Suppl A:S76-84. doi: 10.1053/joca.2001.0448.
Cbfa1 is a transcription factor, which is classified into the runt family. The mice lacking this gene display complete loss of bone formation, indicating that Cbfa1 is an essential factor for osteoblast differentiation. The Cbfa1-deficient mice also show an abnormality in cartilage development. Although cartilage anlagens are well formed in these mice, endochondral ossification is blocked, and most of chondrocytes fail to differentiate into their maturation form as characterized by the absence of type X collagen and low levels of alkaline phosphatase activity. It is suggested that Cbfa1 may participate in chondrocyte differentiation. In this study, we have investigated the role of Cbfa1 in chondrocytes during their cytodifferentiation in vitro.
To investigate the role of Cbfa1 in regulation of chondrocyte differentiation, we over-expressed Cbfa1 or its dominant negative form in cultured chick chondrocytes using a retrovirus (RCAS)system and examined changes in chondrocyte behaviour induced by the introduced genes.
Mature chondrocytes isolated form the cephalic portion of sterna seemed to express Cbfa1 more prominently than immature chondrocytes isolated from the one-third caudal portion of sterna. Over-expression of Cbfa1 in immature chondrocytes strongly stimulated alkaline phosphatase activity and matrix calcification. In contrast, expression of a dominant negative form of Cbfa1, which lacks the C-terminal PST domain, severely inhibited alkaline phosphatase activity and matrix calcification in mature chondrocytes.
Taken together with the observation that Cbfa1 transcripts dominantly localized in hypertrophic chondrocytes as well as in osteoblasts, it is suggested that Cbfa1 plays an important role in the progression of chondrocyte maturation.
Cbfa1是一种转录因子,属于 runt 家族。缺乏该基因的小鼠表现出骨形成完全缺失,这表明Cbfa1是成骨细胞分化的关键因子。Cbfa1基因缺陷的小鼠还表现出软骨发育异常。尽管这些小鼠的软骨原基形成良好,但软骨内骨化受阻,大多数软骨细胞无法分化为成熟形式,其特征是缺乏X型胶原蛋白且碱性磷酸酶活性水平较低。有研究表明Cbfa1可能参与软骨细胞分化。在本研究中,我们调查了Cbfa1在体外软骨细胞分化过程中的作用。
为了研究Cbfa1在软骨细胞分化调控中的作用,我们使用逆转录病毒(RCAS)系统在培养的鸡软骨细胞中过表达Cbfa1或其显性负性形式,并检测导入基因诱导的软骨细胞行为变化。
从胸骨头部分离的成熟软骨细胞似乎比从胸骨尾部三分之一处分离的未成熟软骨细胞更显著地表达Cbfa1。在未成熟软骨细胞中过表达Cbfa1强烈刺激碱性磷酸酶活性和基质钙化。相反,缺乏C末端PST结构域的Cbfa1显性负性形式的表达严重抑制成熟软骨细胞中的碱性磷酸酶活性和基质钙化。
结合Cbfa1转录本主要定位于肥大软骨细胞和成骨细胞的观察结果,提示Cbfa1在软骨细胞成熟进程中起重要作用。