| Literature DB >> 30853186 |
Ryo Aizawa1, Atsushi Yamada2, Tatsuaki Seki3, Junichi Tanaka4, Ryo Nagahama5, Mikiko Ikehata6, Tadashi Kato7, Akiko Sakashita8, Hiroaki Ogata8, Daichi Chikazu9, Koutaro Maki10, Kenji Mishima4, Matsuo Yamamoto3, Ryutaro Kamijo11.
Abstract
Cdc42 (cell division cycle 42) is ubiquitously expressed small GTPases belonging to the Rho family of proteins. Previously, we generated limb bud mesenchyme-specific Cdc42 inactivated mice (Cdc42 conditional knockout mice; Cdc42 fl/fl; Prx1-Cre), which showed short limbs and cranial bone deformities, though the mechanism related to the cranium phenotype was unclear. In the present study, we investigated the role of Cdc42 in cranial bone development. Our results showed that loss of Cdc42 caused a defect of intramembranous ossification in cranial bone tissues which is related to decreased expressions of cranial suture morphogenesis genes, including Indian hedgehog (Ihh) and bone morphogenetic proteins (BMPs). These findings demonstrate that Cdc42 plays a crucial role in cranial osteogenesis, and is controlled by Ihh- and BMP-mediated signaling during cranium development.Entities:
Keywords: Cdc42; Conditional knockout mice; Osteogenesis; Suture
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Year: 2019 PMID: 30853186 DOI: 10.1016/j.bbrc.2019.02.106
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575