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Updated: Jul 12, 2026

Osteoclast Derivation from Mouse Bone Marrow
Published on: November 6, 2014
Oestrogen receptors and linear bone growth
Andrei S Chagin1, Lars Sävendahl
1Pediatric Endocrinology Unit, Department of Woman and Child Health, Karolinska Institutet, Stockholm, Sweden. andrei.chagin@ki.se
Abstract:
In this review we summarize available data regarding linear growth in oestrogen receptor alpha (ERalpha)- and oestrogen receptor beta (ERbeta)-deficient mice. We discuss these findings in relation to known oestrogenic effects in humans and the possibility of applying this knowledge for the therapeutic modulation of longitudinal bone growth employing selective oestrogen receptor modulators (SERMs). We conclude that SERMs potentially could offer new possibilities to modulate bone growth by specifically targeting different oestrogen receptors within the growth plate.
Insights
Selective oestrogen receptor modulators (SERMs) may offer new ways to control bone growth. By targeting specific oestrogen receptors in the growth plate, SERMs could provide therapeutic options for modulating linear growth.
Area of Science:
- Endocrinology
- Bone Biology
- Pharmacology
Background:
- Oestrogen receptors (ERalpha and ERbeta) play crucial roles in regulating longitudinal bone growth.
- Understanding the specific functions of ERalpha and ERbeta in bone development is essential for therapeutic interventions.
- Oestrogenic effects on human bone growth provide a basis for exploring pharmacological modulation.
Purpose of the Study:
- To review available data on linear growth in mice deficient in oestrogen receptor alpha (ERalpha) and oestrogen receptor beta (ERbeta).
- To discuss these findings in the context of human oestrogenic effects on bone growth.
- To explore the potential of selective oestrogen receptor modulators (SERMs) for therapeutic modulation of longitudinal bone growth.
Main Methods:
- Review of existing scientific literature and data.
- Analysis of studies involving ERalpha- and ERbeta-deficient mouse models.
- Correlation of animal model findings with human physiological data.
Main Results:
- Data from ERalpha- and ERbeta-deficient mice provide insights into the distinct roles of these receptors in linear growth.
- Oestrogenic pathways significantly influence longitudinal bone development, as evidenced in mouse models.
- Specific targeting of oestrogen receptors is feasible.
Conclusions:
- Selective oestrogen receptor modulators (SERMs) show promise for modulating bone growth.
- Targeting specific oestrogen receptors within the growth plate offers a potential therapeutic strategy.
- SERMs could represent a novel approach to managing conditions related to abnormal longitudinal bone growth.
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