| Literature DB >> 27993989 |
Naoki Koda1,2, Tempei Sato1, Masahiro Shinohara1,3, Shizuko Ichinose4, Yoshiaki Ito1, Ryo Nakamichi1, Tomohiro Kayama1, Kensuke Kataoka1, Hidetsugu Suzuki1, Keiji Moriyama2, Hiroshi Asahara5,6.
Abstract
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.Entities:
Keywords: Collagen; Mohawk; Mouse; Osteogenic change; PDL homeostasis
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Year: 2016 PMID: 27993989 PMCID: PMC5394762 DOI: 10.1242/dev.135798
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868