Estrogen depletion alters osteogenic differentiation and matrix production by osteoblasts in vitro
Experimental Cell Research, ISSN: 0014-4827, Vol: 408, Issue: 1, Page: 112814
2021
- 12Citations
- 23Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations12
- Citation Indexes12
- 12
- CrossRef7
- Captures23
- Readers23
- 23
Article Description
Recent studies have revealed that the effects of estrogen deficiency are not restricted to osteoclasts and bone resorption, but that bone matrix composition is altered and osteoblasts exhibit an impaired response to mechanical stimulation. In this study, we test the hypothesis that estrogen depletion alters osteogenic differentiation and matrix production by mechanically stimulated osteoblasts in vitro. MC3T3-E1 cells were pre-treated with estrogen for 14 days, after which estrogen was withdrawn or inhibited with Fulvestrant up to 14 days. Fluid shear stress (FSS) was applied using an orbital shaker. Under estrogen depletion in static culture, osteogenic marker (ALP) and gene expression ( Runx2 ) were decreased at 2 and after 7 days of estrogen depletion, respectively. In addition, up to 7 day the inhibition of the estrogen receptor significantly decreased fibronectin expression ( FN1 ) under static conditions. Under estrogen depletion and daily mechanical stimulation, changes in expression of Runx2 occurred earlier (4 days) and by 14 days, changes in matrix production ( Col1a1 ) were reported. We propose that changes in osteoblast differentiation and impaired matrix production during estrogen depletion may contribute to the altered quality of the bone and act as a contributing factor to increased bone fragility in postmenopausal osteoporosis.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0014482721003682; http://dx.doi.org/10.1016/j.yexcr.2021.112814; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85116546738&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34492267; https://linkinghub.elsevier.com/retrieve/pii/S0014482721003682; https://dx.doi.org/10.1016/j.yexcr.2021.112814
Elsevier BV
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