Cdc42 regulates cranial suture morphogenesis and ossification.

Authors :: Aizawa R
Yamada A
Seki T
Tanaka J
Nagahama R
Ikehata M
Kato T
Sakashita A
Ogata H
Chikazu D
Maki K
Mishima K
Yamamoto M
Kamijo R
Source :: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2019 Apr 30; Vol. 512 (2), pp. 145-149. Date of Electronic Publication: 2019 Mar 07.
Publication Year :: 2019
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 <superscript> fl/fl</superscript> ; 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.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)