Department of Oral and Maxillofacial Rehabilitation, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8525, Japan.
Arch Oral Biol. 2013 Nov;58(11):1659-66. doi: 10.1016/j.archoralbio.2013.08.010. Epub 2013 Aug 31.
CCN proteins are extracellular and cell-associated molecules involved in several developmental processes, but their expression patterns and regulation in tooth development remain unclear. Here we first determined the expression patterns of CCN genes in mouse tooth germs. We found that at early stages CCN2 was detected in dental lamina, dental mesenchyme, and primary enamel knot, while other CCN family members were expressed broadly. By the bell stage, all members were expressed in differentiating odontoblasts and ameloblasts, but CCN1 and CCN2 transcripts were conspicuous in differentiating osteoblasts in dental follicle. Next, we asked what signalling molecules regulate CCN2 expression and what roles CCN2 may have. We found that upon surgical removal of dental epithelium CCN2 was not longer expressed in dental mesenchyme in cultured bud stage germs. Implantation of beads pre-coated with BMPs and FGFs onto E12-13 mandibular explants induced CCN2 expression in dental mesenchyme. There was a dose-dependent effect of BMP-4 on CCN2 induction; a concentration of 100 ng/μl was able to induce strong CCN2 expression while a minimum concentration of 25 ng/μl was needed to elicit appreciable expression. Importantly, Noggin treatment inhibited endogenous and BMP-induced CCN2 expression, verifying that CCN2 expression in developing tooth germs requires BMP signalling. Lastly, we found that rCCN2 stimulated proliferation in dental mesenchyme in a dose-dependent manner. Together, the data indicate that expression of CCN genes is spatio-temporally regulated in developing tooth germs. CCN2 expression appears to depend on epithelial and mesenchymal-derived signalling factors, and CCN2 can elicit strong proliferation in dental mesenchyme.
CCN 蛋白是细胞外和细胞相关的分子,参与多种发育过程,但它们在牙齿发育中的表达模式和调节仍不清楚。在这里,我们首先确定了 CCN 基因在小鼠牙胚中的表达模式。我们发现,在早期阶段,CCN2 被检测到在牙板、牙间质和初级釉结中表达,而其他 CCN 家族成员则广泛表达。在钟状期,所有成员都在分化的成牙本质细胞和成釉细胞中表达,但 CCN1 和 CCN2 转录物在牙滤泡中分化的成骨细胞中很明显。接下来,我们询问是什么信号分子调节 CCN2 的表达,以及 CCN2 可能扮演什么角色。我们发现,在牙上皮被手术切除后,培养的芽期牙胚中的牙间质中不再表达 CCN2。将预先包被 BMP 和 FGF 的珠子植入 E12-13 下颌离体组织中,诱导牙间质中 CCN2 的表达。BMP-4 对 CCN2 诱导有剂量依赖性效应;100ng/μl 的浓度能够诱导强烈的 CCN2 表达,而 25ng/μl 的最低浓度足以引起可观的表达。重要的是, Noggin 处理抑制了内源性和 BMP 诱导的 CCN2 表达,证实了 CCN2 在发育中的牙胚中的表达需要 BMP 信号。最后,我们发现 rCCN2 以剂量依赖的方式刺激牙间质的增殖。总之,数据表明 CCN 基因在发育中的牙胚中时空调节表达。CCN2 的表达似乎依赖于上皮和间质衍生的信号因子,CCN2 可以在牙间质中引起强烈的增殖。