Okahata Saori, Yamamoto Ryuji, Yamakoshi Yasuo, Fukae Makoto
Department of Periodontics and Endodontics, Tsurumi University, 2-1-3 Tsurumi-ku, Yokohama, Japan.
J Oral Biosci. 2011;53(1):72-81. doi: 10.2330/joralbiosci.53.72.
Proteoglycans and their constituent glycosaminoglycan (GAG) have been proposed to be involved in the inhibition of mineralization in unmineralized tissue, predentin. Among the proteoglycans secreted by odontoblasts, we focused on the large chondroitin sulfate proteoglycan, versican, for its large binding capacity for calcium ions. The aims of this study were the determination of the full-length sequence and splicing variants of the porcine versican, and the detection of versican in the porcine predentin. The complete coding sequence of the porcine versican mRNA was cloned to be 11,775 nucleotides long and encode 3,924 amino acids, and four splicing variants, V0, V1, V2 and V3, were characterized in the isolated porcine cartilage cells. The number of potential GAG attachment sites was 15 in the V0 variant, 13 in the V1 variant, 2 in the V2 variant and 0 in the V3 variant. They were deposited in DDBJ. The V1 variant was determined by RT-PCR in the odontoblasts, dental papilla cells, dental follicle cells, periodontal ligament cells, dental pulp cells, and gingival cells of pigs, although a small amount of the V0 valiant was found in the dental papilla cells. The predentin was prepared from developing porcine permanent incisor tooth germs and its soluble proteins were extracted in order to be partially characterized by protein and proteinase profiles. The versican V1 cleavage products were detected in the predentin extract by Western blotting analysis. These results suggested that the versican splice variant V1 implicates both the control of the mineralization and the activities of the predentin metalloproteinases, because it has 13 GAG chains that bind a large amount of calcium.
蛋白聚糖及其组成的糖胺聚糖(GAG)被认为参与了未矿化组织前期牙本质中矿化的抑制过程。在成牙本质细胞分泌的蛋白聚糖中,我们聚焦于硫酸软骨素蛋白聚糖versican,因为它对钙离子具有较大的结合能力。本研究的目的是确定猪versican的全长序列和剪接变体,并检测猪前期牙本质中的versican。猪versican mRNA的完整编码序列被克隆出来,长度为11775个核苷酸,编码3924个氨基酸,并且在分离的猪软骨细胞中鉴定出了四种剪接变体V0、V1、V2和V3。V0变体中潜在的GAG附着位点有15个,V1变体中有13个,V2变体中有2个,V3变体中为0个。它们已存入日本DNA数据库(DDBJ)。通过逆转录聚合酶链反应(RT-PCR)在猪的成牙本质细胞、牙乳头细胞、牙囊细胞、牙周膜细胞、牙髓细胞和牙龈细胞中检测到了V1变体,尽管在牙乳头细胞中发现了少量的V0变体。从发育中的猪恒切牙牙胚制备前期牙本质,并提取其可溶性蛋白,以便通过蛋白质和蛋白酶谱进行部分表征。通过蛋白质印迹分析在前期牙本质提取物中检测到了versican V1的裂解产物。这些结果表明,versican剪接变体V1既参与了矿化的调控,也参与了前期牙本质金属蛋白酶的活性调控,因为它有13条能结合大量钙离子的GAG链。