Skeletal Effects of Inducible ER? Deletion in Osteocytes in Adult Mice


Estrogen is known to regulate bone metabolism in both women and men, but substantial gaps remain in our knowledge of estrogen and estrogen receptor alpha (ER?) regulation of adult bone metabolism. Studies using global ER?-knockout mice were confounded by high circulating sex-steroid levels, and osteocyte/osteoblast-specific ER? deletion may be confounded by ER? effects on growth versus the adult skeleton. Thus, we developed mice expressing the tamoxifen-inducible CreERT2 in osteocytes using the 8-kilobase (kb) Dmp1 promoter (Dmp1CreERT2). These mice were crossed with ER?fl//fl mice to create ER??Ocy mice, permitting inducible osteocyte-specific ER? deletion in adulthood. After intermittent tamoxifen treatment of adult 4-month-old mice for 1?month, female, but not male, ER??Ocy mice exhibited reduced spine bone volume fraction (BV/TV (?20.1%, p = 0.004) accompanied by decreased trabecular bone formation rate (?18.9%, p = 0.0496) and serum P1NP levels (?38.9%, p = 0.014). Periosteal (+65.6%, p = 0.004) and endocortical (+64.1%, p = 0.003) expansion were higher in ER??Ocy mice compared to control (Dmp1CreERT2) mice at the tibial diaphysis, reflecting the known effects of estrogen to inhibit periosteal apposition and promote endocortical formation. Increases in Sost (2.1-fold, p = 0.001) messenger RNA (mRNA) levels were observed in trabecular bone at the spine in ER??Ocy mice, consistent with previous reports that estrogen deficiency is associated with increased circulating sclerostin as well as bone SOST mRNA levels in humans. Further, the biological consequences of increased Sost expression were reflected in significant overall downregulation in panels of osteoblast and Wnt target genes in osteocyte-enriched bones from ER??Ocy mice. These findings thus establish that osteocytic ER? is critical for estrogen action in female, but not male, adult bone metabolism. Moreover, the reduction in bone formation accompanied by increased Sost, decreased osteoblast, and decreased Wnt target gene expression in ER??Ocy mice provides a direct link in vivo between ER? and Wnt signaling. © 2022 American Society for Bone and Mineral Research (ASBMR).