Suardita Ketut, Fujimoto Katsumi, Oda Ryo, Shimazu Atsushi, Miyazaki Kazuko, Kawamoto Takeshi, Kato Yukio
Department of Dental and Medical Biochemistry, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Japan.
J Biol Chem. 2002 Dec 13;277(50):48579-86. doi: 10.1074/jbc.M209243200. Epub 2002 Oct 8.
Membrane-bound transferrin-like protein (MTf) is expressed in parallel with the expression of cartilage-characteristic genes during differentiation of chondrocytes, and the MTf level is much higher in cartilage than in other tissues. To investigate the role of MTf in cartilage, we examined the effects of growth factors on MTf expression in mouse prechondrogenic ATDC5 cells and the effect of MTf overexpression on differentiation of ATDC5 and mouse pluripotent mesenchymal C3H10T1/2 cells. In ATDC5 cultures, bone morphogenetic protein-2 and transforming growth factor-beta as well as insulin induced MTf mRNA expression when these peptides induced chondrogenic differentiation. Forced expression of rabbit MTf in ATDC5 cells induced aggrecan, type II collagen, matrilin-1, type X collagen mRNAs, and cell-shape changes from fibroblastic cells to spherical chondrocytes. Accordingly, the synthesis and accumulation of proteoglycans were higher in MTf-expressing cultures than in control cultures. These effects of MTf overexpression correlated with the MTf protein level on the cell surface and decreased in the presence of anti-MTf antibody. However, the aggrecan mRNA level in the ATDC5 cells overexpressing MTf was lower than that in wild type ATDC5 cells exposed to 10 microg/ml insulin. MTf overexpression in C3H10T1/2 cells also induced aggrecan and/or type II collagen mRNA but not the spherical phenotype. These findings suggest that the expression of MTf on the cell surface facilitates the differentiation of prechondrogenic cells, although MTf overexpression alone seems to be insufficient to commit pluripotent mesenchymal cells to the chondrocyte lineage.
膜结合转铁蛋白样蛋白(MTf)在软骨细胞分化过程中与软骨特征性基因的表达平行,且MTf在软骨中的水平远高于其他组织。为了研究MTf在软骨中的作用,我们检测了生长因子对小鼠软骨前体细胞ATDC5中MTf表达的影响,以及MTf过表达对ATDC5和小鼠多能间充质细胞C3H10T1/2分化的影响。在ATDC5培养物中,骨形态发生蛋白-2、转化生长因子-β以及胰岛素在诱导软骨分化时可诱导MTf mRNA表达。在ATDC5细胞中强制表达兔MTf可诱导聚集蛋白聚糖、II型胶原、基质连接蛋白-1、X型胶原mRNA表达,并使细胞形态从成纤维细胞样转变为球形软骨细胞。因此,在表达MTf的培养物中蛋白聚糖的合成和积累高于对照培养物。MTf过表达的这些作用与细胞表面的MTf蛋白水平相关,且在抗MTf抗体存在时作用减弱。然而,过表达MTf的ATDC5细胞中聚集蛋白聚糖mRNA水平低于暴露于10μg/ml胰岛素的野生型ATDC5细胞。在C3H10T1/2细胞中过表达MTf也可诱导聚集蛋白聚糖和/或II型胶原mRNA表达,但不会诱导形成球形表型。这些发现表明,细胞表面MTf的表达促进软骨前体细胞的分化,尽管单独的MTf过表达似乎不足以使多能间充质细胞定向分化为软骨细胞谱系。