Cdc42 regulates cranial suture morphogenesis and ossification.
Aizawa, Ryo; Yamada, Atsushi; Seki, Tatsuaki; Tanaka, Junichi; Nagahama, Ryo; Ikehata, Mikiko; Kato, Tadashi; Sakashita, Akiko; Ogata, Hiroaki; Chikazu, Daichi; Maki, Koutaro; Mishima, Kenji; Yamamoto, Matsuo; Kamijo, Ryutaro.
Biochem Biophys Res Commun;
512(2): 145-149, 2019 04 30.
Inglês
| MEDLINE
| ID: mdl-30853186
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; Cdc42â¯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.
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