Literature DB >> 30853186

Cdc42 regulates cranial suture morphogenesis and ossification.

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.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cdc42; Conditional knockout mice; Osteogenesis; Suture

Mesh:

Substances:

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


  1 in total

Review 1.  Molecular mechanisms of intermuscular bone development in fish: a review.

Authors:  Bo Li; Yuan-Wei Zhang; Xiao Liu; Li Ma; Jun-Xing Yang
Journal:  Zool Res       Date:  2021-05-18
  1 in total

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