Estrogen facilitates osteoblast differentiation by upregulating bone morphogenetic protein-4 signaling

Yoshinori Matsumoto, Fumio Otsuka, Mariko Takano-Narazaki, Takayuki Katsuyama, Eri Nakamura, Naoko Tsukamoto, Kenichi Inagaki, Kenei Sada, Hirofumi Makino

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Imbalanced functions of osteoclasts and osteoblasts are involved in various types of bone damage including postmenopausal osteoporosis. In the present study, we investigated the cellular mechanism by which estrogen interacts in the process of osteoblastic differentiation regulated by BMP-4 using mouse MC3T3-E1 cells that express estrogen receptors (ER) and BMP-4. Estradiol enhanced BMP-4-induced Runx2, osterix, ALP and osteocalcin expression in MC3T3-E1 cells. BMP-4-induced mineralization shown by Alizarin red staining was also facilitated by estrogen treatment. It was revealed that estrogen upregulated BMP-4-induced Smad1/5/8 phosphorylation, BRE-Luc activity and Id-1 mRNA expression. The expression of BMPRII was increased by estrogen in MC3T3-E1 cells, and inhibition of BMPRII or ALK-2/3 signaling impaired the effect of estrogen on BMP-4 signaling. Of note, the enhanced expression of osterix, ALP and osteocalcin mRNAs induced by BMP-4 and estrogen was reversed in the presence of an ER antagonist. Given that membrane-impermeable estrogen also upregulated BMP-4-induced expression of osteoblastic markers and Id-1 mRNA, non-genomic ER activity is involved in the mechanism by which estrogen enhances BMP-4-induced osteoblast differentiation in MC3T3-E1 cells. On the other hand, the expression of ERα and endogenous BMP-4 was suppressed by BMP-4 treatment regardless of the presence of estrogen, implying the presence of a negative feedback loop for osteoblast differentiation. Thus, estrogen is functionally involved in the process of osteoblast differentiation regulated by BMP-4 through upregulating BMP sensitivity of MC3T3-E1 cells.

Original languageEnglish
Pages (from-to)513-520
Number of pages8
JournalSteroids
Volume78
Issue number5
DOIs
Publication statusPublished - May 2013

Fingerprint

Bone Morphogenetic Protein 4
Osteoblasts
Estrogens
Estrogen Receptors
Osteocalcin
Messenger RNA
Postmenopausal Osteoporosis
Phosphorylation
Osteoclasts
Estradiol
Bone

Keywords

  • Bone morphogenetic protein (BMP)
  • Estradiol
  • Estrogen
  • Estrogen receptor (ER)
  • Mineralization
  • Osteoblast differentiation

ASJC Scopus subject areas

  • Biochemistry
  • Clinical Biochemistry
  • Endocrinology
  • Molecular Biology
  • Organic Chemistry
  • Pharmacology

Cite this

Estrogen facilitates osteoblast differentiation by upregulating bone morphogenetic protein-4 signaling. / Matsumoto, Yoshinori; Otsuka, Fumio; Takano-Narazaki, Mariko; Katsuyama, Takayuki; Nakamura, Eri; Tsukamoto, Naoko; Inagaki, Kenichi; Sada, Kenei; Makino, Hirofumi.

In: Steroids, Vol. 78, No. 5, 05.2013, p. 513-520.

Research output: Contribution to journalArticle

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