Rho-GEF trio regulates osteoclast differentiation and function by Rac1/Cdc42.
Exp Cell Res
; 396(1): 112265, 2020 11 01.
Article
in En
| MEDLINE
| ID: mdl-32898553
ABSTRACT
Many bone diseases result from abnormal bone resorption by osteoclasts (OCs). Studying OC related regulatory genes is necessary for the development of new therapeutic strategies. Rho GTPases have been proven to regulate OC differentiation and function and only mature OCs can carry out bone resorption. Here we demonstrate that Rac1 and Cdc42 exchange factor Triple functional domain (Trio) is critical for bone resorption caused by OCs. In this study, we created LysM-Cre;Triofl/fl conditional knockout mice in which Trio was conditionally ablated in monocytes. LysM-Cre;Triofl/fl mice showed increased bone mass due to impaired bone resorption caused by OCs. Furthermore, our in vitro analysis indicated that Trio conditional deficiency significantly suppressed OC differentiation and function. At the molecular level, Trio deficiency significantly inhibited the expression of genes critical for osteoclastogenesis and OC function. Mechanistically, our researches suggested that perturbed Rac1/Cdc42-PAK1-ERK/p38 signaling could be used to explain the lower ability of bone resorption in CKO mice. Taken together, this study indicates that Trio is a regulator of OCs. Studying the role of Trio in OCs provides a potential new insight for the treatment of OC related bone diseases.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Osteoclasts
/
Phosphoproteins
/
Bone Resorption
/
Neuropeptides
/
Protein Serine-Threonine Kinases
/
Cdc42 GTP-Binding Protein
/
Rac1 GTP-Binding Protein
/
Guanine Nucleotide Exchange Factors
/
Femur
Type of study:
Prognostic_studies
Limits:
Animals
Language:
En
Journal:
Exp Cell Res
Year:
2020
Document type:
Article