Osteoclast differentiation and dynamic mRNA expression during mice embryonic palatal bone development

• Published in: Scientific reports Vol. 13; no. 1; pp. 15170 - 14
• Main Authors: Lai, Yongzhen, Guo, Yan, Liao, Caiyu, Mao, Chuanqing, Liu, Jing, Ren, Chengyan, Yang, Wen, Luo, Lin, Chen, Weihui
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13-09-2023; Nature Publishing Group; Nature Portfolio
• Subjects: 1-Phosphatidylinositol 3-kinase; 631/136/1455; 631/136/2086; 631/136/815; 631/136/818; 631/136/83; AKT protein; Bone growth; Bone marrow; Bone remodeling; Down-regulation; Embryogenesis; Fc receptors; Gene expression; Humanities and Social Sciences; Kinases; Laboratory animals; MAP kinase; Maternal & child health; Maxilla; Mineralization; multidisciplinary; Osteoclastogenesis; Palate; Science; Science (multidisciplinary); Signal transduction
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-42423-4

This study is the first to investigate the process of osteoclast (OCL) differentiation, its potential functions, and the associated mRNA and signalling pathways in embryonic palatal bone. Our findings suggest that OCLs are involved in bone remodelling, bone marrow cavity formation, and blood vessel formation in embryonic palatal bone. We observed TRAP-positive OCLs at embryonic day 16.5 (E16.5), E17.5, and E18.5 at the palatal process of the palate (PPP) and posterior and anterior parts of the palatal process of the maxilla (PPMXP and PPMXA, respectively), with OCL differentiation starting 2 days prior to TRAP positivity. By comparing the key periods of OCL differentiation between PPMX and PPP (E14.5, E15.5, and E16.5) using RNA-seq data of the palates, we found that the PI3K-AKT and MAPK signalling pathways were sequentially enriched, which may play critical roles in OCL survival and differentiation. Csf1r, Tnfrsff11a, Ctsk, Fos, Tyrobp, Fcgr3, and Spi1 were significantly upregulated, while Pik3r3, Tgfbr1, and Mapk3k7 were significantly downregulated, in both PPMX and PPP. Interestingly, Tnfrsff11b was upregulated in PPMX but downregulated in PPP, which may regulate the timing of OCL appearance. These results contribute to the limited knowledge regarding mRNA-specific steps in OCL differentiation in the embryonic palatal bone.