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Published on: June 2, 2020
Osteoclasts isolated from membranous bone in children exhibit nuclear estrogen and progesterone receptors
J M Pensler1, J A Radosevich, R Higbee
1Department of Surgery, Northwestern University Medical School, Chicago, IL 60614.
Insights
Sex steroid hormones, estrogen and progesterone, directly influence bone resorption. Researchers found nuclear receptors for these hormones in children's osteoclasts, suggesting a direct mechanism for hormone action on bone.
Area of Science:
- Endocrinology
- Cell Biology
- Orthopedics
Background:
- Osteoclasts are critical for bone remodeling and resorption.
- The role of sex steroid hormones in bone metabolism is well-established, but direct mechanisms in osteoclasts are less understood.
Purpose of the Study:
- To investigate the presence and function of sex steroid hormone receptors in human osteoclasts from children.
- To explore the potential for direct hormonal modulation of bone resorption.
Main Methods:
- Isolation of osteoclasts from membranous bone of pediatric patients undergoing craniotomy.
- Functional assays including tartrate-resistant acid phosphatase production and resorption lacunae formation.
- Immunohistochemical detection and radioimmunoassay quantification of nuclear estrogen and progesterone receptors.
Main Results:
- Isolated osteoclasts exhibited characteristic bone resorption functions.
- Nuclear estrogen and progesterone receptors were successfully identified and quantified in osteoclasts.
- Receptor presence suggests a direct pathway for sex steroid hormone influence on osteoclast activity.
Conclusions:
- Human osteoclasts possess nuclear receptors for estrogen and progesterone.
- This finding supports a direct mechanism by which sex steroid hormones can modulate bone resorption in children.
- Establishes a potential cellular basis for hormonal effects on bone health and disease.
Abstract:
Osteoclasts were isolated from membranous bone from four children without metabolic bone disease who were undergoing craniotomy for either tumor or trauma. Both freshly isolated osteoclasts and those cultured for 4-7 days exhibited the following characteristics: production of tartrate-resistant acid phosphatase (9.5-14.8 units), contraction in response to application of 100 mg/ml of human calcitonin, and formation of resorption lacunae on devitalized bone wafers. Nuclear estrogen and progesterone receptors were demonstrated by immunohistochemical techniques and quantitated in two of the patients by radioimmunoassay (estrogen receptor RIA, 23.6 and 23.8 cpm/micrograms protein; progesterone receptor RIA, 36.7 and 74.2 cpm/micrograms protein). The demonstration of sex steroid hormone receptors in the nucleus of osteoclasts derived from children with normal membranous bone has established a potential mechanism whereby direct modulation of bone resorption by the sex steroid estrogen and progesterone may occur.
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