Koda Naoki, Sato Tempei, Shinohara Masahiro, Ichinose Shizuko, Ito Yoshiaki, Nakamichi Ryo, Kayama Tomohiro, Kataoka Kensuke, Suzuki Hidetsugu, Moriyama Keiji, Asahara Hiroshi
Department of Systems BioMedicine, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Maxillofacial Orthognathics, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
Development. 2017 Jan 15;144(2):313-320. doi: 10.1242/dev.135798. Epub 2016 Dec 19.
The periodontal ligament (PDL), which connects the teeth to the alveolar bone, is essential for periodontal tissue homeostasis. Although the significance of the PDL is recognized, molecular mechanisms underlying PDL function are not well known. We report that mohawk homeobox (Mkx), a tendon-specific transcription factor, regulates PDL homeostasis by preventing its degeneration. Mkx is expressed in the mouse PDL at the age of 10 weeks and expression remained at similar levels at 12 months. In Mkx mice, age-dependent expansion of the PDL at the maxillary first molar (M1) furcation area was observed. Transmission electron microscopy (TEM) revealed that Mkx mice presented collagen fibril degeneration in PDL with age, while the collagen fibril diameter gradually increased in Mkx mice. PDL cells lost their shape in Mkx mice, suggesting changes in PDL properties. Microarray and quantitative polymerase chain reaction (qPCR) analyses of Mkx PDL revealed an increase in osteogenic gene expression and no change in PDL- and inflammatory-related gene expression. Additionally, COL1A1 and COL1A2 were upregulated in Mkx-overexpressing human PDL fibroblasts, whereas osteogenic genes were downregulated. Our results indicate that Mkx prevents PDL degeneration by regulating osteogenesis.
连接牙齿与牙槽骨的牙周韧带(PDL)对于牙周组织的稳态至关重要。尽管PDL的重要性已得到认可,但其功能的分子机制尚不明确。我们报告称,肌腱特异性转录因子莫霍克同源框(Mkx)通过防止PDL退变来调节其稳态。Mkx在10周龄小鼠的PDL中表达,并在12个月时保持在相似水平。在Mkx基因敲除小鼠中,观察到上颌第一磨牙(M1)分叉区的PDL随年龄增长而扩张。透射电子显微镜(TEM)显示,随着年龄增长,Mkx基因敲除小鼠的PDL中出现胶原纤维退变,而Mkx基因敲除小鼠的胶原纤维直径逐渐增加。在Mkx基因敲除小鼠中,PDL细胞失去了其形态,提示PDL特性发生了变化。对Mkx基因敲除小鼠的PDL进行微阵列和定量聚合酶链反应(qPCR)分析,结果显示成骨基因表达增加,而与PDL和炎症相关的基因表达没有变化。此外,在过表达Mkx的人PDL成纤维细胞中,COL1A1和COL1A被上调,而成骨基因被下调。我们的结果表明,Mkx通过调节成骨作用来防止PDL退变。