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Knocking out FAM20C in pre-osteoblasts leads to up-regulation of osteoclast differentiation to affect long bone development.

Authors :
Jiang, Lili
Liu, Xinpeng
Liu, Lixue
Su, Lide
Lu, Zeyu
Zhang, Hong
Guo, Yuyao
Zhang, Wenxuan
Zhang, Shujian
Xu, Wenxia
Zhang, Jiahui
Zhang, Kai
Zhan, Yuanbo
Xie, Xiaohua
Li, Runhang
Dong, Xinhe
Jin, Han
Zhang, Bin
Li, Ying
Source :
Gene. Jul2024, Vol. 915, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

• FAM20C phosphorylates regulatory proteins involved in bone development. • A novel Osx-Cre; FAM20Cflox/flox knockout (oKO) mouse model is established. • oKO has lower bone mineralization, along with greater hypertrophic cartilage. • oKO has up-regulation of osteoclast differentiation genes Sirpb1a-c and Mapk13. • Osteogenesis-related genes Osx, Alp, Ocn, Mepe, and Col2 are downregulated in oKO. Family with sequence similarity 20 member C (FAM20C) is a Golgi casein kinase that phosphorylates extracellularly-secreted regulatory proteins involved in bone development and mineralization, but its specific role in bone development is still largely unknown. In this study, to examine the specific mechanisms that FAM20C influences bone development, we cross-bred Osx-Cre with FAM20Cflox/flox mice to establish a Osx-Cre; FAM20Cflox/flox knockout (oKO) mouse model; FAM20C was KO in pre-osteoblasts. oKO development was examined at 1–10 weeks, in which compared to control FAM20Cflox/flox, they had lower body weights and bone tissue mineralization. Furthermore, oKO had lower bone volume fractions, thickness, and trabecular numbers, along with higher degrees of trabecular separation. These mice also had decreased femoral metaphyseal cartilage proliferation layer, along with thickened hypertrophic layer and increased apoptotic cell counts. Transcriptomic analysis found that differentially-expressed genes in oKO were concentrated in the osteoclast differentiation pathway, in line with increased osteoclast presence. Additionally, up-regulation of osteoclast-related, and down-regulation of osteogenesis-related genes, were identified, in which the most up-regulated genes were signal regulatory protein β-1 family (Sirpb1a-c) and mitogen-activated protein kinase 13. Overall, FAM20C KO in pre-osteoblasts leads to abnormal long bone development, likely due to subsequent up-regulation of osteoclast differentiation-associated genes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03781119
Volume :
915
Database :
Academic Search Index
Journal :
Gene
Publication Type :
Academic Journal
Accession number :
176992149
Full Text :
https://doi.org/10.1016/j.gene.2024.148396