Osteoblastic Lrp4 promotes osteoclastogenesis by regulating ATP release and adenosine-A_2AR signaling.

ABSTRACT: Bone homeostasis depends on the functional balance of osteoblasts (OBs) and osteoclasts (OCs). Lrp4 is a transmembrane protein that is mutated in patients with high bone mass. Loss of Lrp4 in OB-lineage cells increases bone mass by elevating bone formation by OBs and reducing bone resorption by OCs. However, it is unclear how Lrp4 deficiency in OBs impairs osteoclastogenesis. Here, we provide evidence that loss of Lrp4 in the OB lineage stabilizes the prorenin receptor (PRR) and increases PRR/V-ATPase-driven ATP release, thereby enhancing the production of the ATP derivative adenosine. Both pharmacological and genetic inhibition of adenosine-_2A receptor (A_2AR) in culture and Lrp4 mutant mice diminishes the osteoclastogenic deficit and reduces trabecular bone mass. Fur

SUBMITTER: Xiong L 

PROVIDER: S-EPMC5350517 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature