Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice

Shino Kondoh, Kazuki Inoue, Katsuhide Igarashi, Hiroe Sugizaki, Yuko Shirode-Fukuda, Erina Inoue, Taiyong Yu, Jun K. Takeuchi, Jun Kanno, Lynda Bonewald, Yuuki Imai

Research output: Contribution to journalArticle

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Abstract

Estrogens are well known steroid hormones necessary to maintain bone health. In addition, mechanical loading, in which estrogen signaling may intersect with the Wnt/β-catenin pathway, is essential for bone maintenance. As osteocytes are known as the major mechanosensory cells embedded in mineralized bone matrix, osteocyte ERα deletion mice (ERαδOcy/δOcy) were generated by mating ERα floxed mice with Dmp1-Cre mice to determine the role of ERα in osteocytes. Trabecular bone mineral density of female, but not male ERαδOcy/δOcy mice was significantly decreased. Bone formation parameters in ERαδOcy/δOcy were significantly decreased while osteoclast parameters were unchanged. This suggests that ERα in osteocytes exerts osteoprotective function by positively controlling bone formation. To identify potential targets of ERα, gene array analysis of Dmp1-GFP osteocytes sorted by FACS from ERαδOcy/δOcy and control mice was performed. Gene expression microarray followed by gene ontology analyses revealed that osteocytes from ERαδOcy/δOcy highly expressed genes categorized in 'Secreted' when compared to control osteocytes. Among them, expression of Mdk and Sostdc1, both of which are Wnt inhibitors, was significantly increased without alteration of expression of the mature osteocyte markers such as Sost and β-catenin. Moreover, hindlimb suspension experiments showed that trabecular bone loss due to unloading was greater in ERαδOcy/δOcy mice without cortical bone loss. These data suggest that ERα in osteocytes has osteoprotective functions in trabecular bone formation through regulating expression of Wnt antagonists, but conversely plays a negative role in cortical bone loss due to unloading.

Original languageEnglish (US)
Pages (from-to)68-77
Number of pages10
JournalBone
Volume60
DOIs
StatePublished - Mar 2014
Externally publishedYes

Fingerprint

Osteocytes
Osteogenesis
Estrogen Receptors
Catenins
Estrogens
Hindlimb Suspension
Cancellous Bone
Bone and Bones
Gene Ontology
Bone Matrix
Wnt Signaling Pathway
Osteoclasts
Bone Density
Genes
Steroids
Maintenance
Hormones
Gene Expression

Keywords

  • Bone formation
  • Estrogen
  • Estrogen receptor α
  • Osteocyte
  • Wnt signaling

ASJC Scopus subject areas

  • Physiology
  • Endocrinology, Diabetes and Metabolism
  • Histology

Cite this

Kondoh, S., Inoue, K., Igarashi, K., Sugizaki, H., Shirode-Fukuda, Y., Inoue, E., ... Imai, Y. (2014). Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice. Bone, 60, 68-77. https://doi.org/10.1016/j.bone.2013.12.005

Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice. / Kondoh, Shino; Inoue, Kazuki; Igarashi, Katsuhide; Sugizaki, Hiroe; Shirode-Fukuda, Yuko; Inoue, Erina; Yu, Taiyong; Takeuchi, Jun K.; Kanno, Jun; Bonewald, Lynda; Imai, Yuuki.

In: Bone, Vol. 60, 03.2014, p. 68-77.

Research output: Contribution to journalArticle

Kondoh, S, Inoue, K, Igarashi, K, Sugizaki, H, Shirode-Fukuda, Y, Inoue, E, Yu, T, Takeuchi, JK, Kanno, J, Bonewald, L & Imai, Y 2014, 'Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice', Bone, vol. 60, pp. 68-77. https://doi.org/10.1016/j.bone.2013.12.005
Kondoh S, Inoue K, Igarashi K, Sugizaki H, Shirode-Fukuda Y, Inoue E et al. Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice. Bone. 2014 Mar;60:68-77. https://doi.org/10.1016/j.bone.2013.12.005
Kondoh, Shino ; Inoue, Kazuki ; Igarashi, Katsuhide ; Sugizaki, Hiroe ; Shirode-Fukuda, Yuko ; Inoue, Erina ; Yu, Taiyong ; Takeuchi, Jun K. ; Kanno, Jun ; Bonewald, Lynda ; Imai, Yuuki. / Estrogen receptor α in osteocytes regulates trabecular bone formation in female mice. In: Bone. 2014 ; Vol. 60. pp. 68-77.
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