In the mouse, ovariectomy (OVX) leads to signi®cant reductions in cancellous bone volume while estrogen (17b-estradiol, E2) replacement not only prevents bone loss but can increase bone formation. As the E2dependent increase in bone formation would require the proliferation and differentiation of os
Estrogen stimulates differentiation of megakaryocytes and modulates their expression of estrogen receptors α and β
✍ Scribed by Sharyn Bord; Emma Frith; Deborah C. Ireland; Mike A. Scott; Jenny I.O. Craig; Juliet E. Compston
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 203 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Estrogen has multifunctional effects influencing growth, differentiation, and function in many tissues. High‐dose estrogen has been shown to produce anabolic skeletal effects in the skeleton of postmenopausal women with increased megakaryocyte (MK) population in the bone marrow, suggesting a possible role for these cells in bone remodelling. To investigate if estrogen stimulates megakaryocytopoiesis and affects on estrogen receptor (ER) expression, CD34(+) cells were cultured for 6, 9, and 14 days plus or minus low‐dose or high‐dose 17β estradiol (E). Cells were immunolocalised for CD61, CD41, ERα and β. ER mRNA expression was assessed by RT‐PCR. Cells formed more CD61 positive MK colonies with low‐ and high‐dose E treatment (P < 0.001) at 6 and 9 days. CD41 expression was increased dose‐dependently in MK (3‐ and 5‐fold P < 0.001) at 9 days. E‐stimulated ERα expression at 6 days (P < 0.001) whilst ERβ was dose‐dependently increased only at 9 days (P < 0.01). ERα mRNA was increased at 6 days but not at 14 days whilst ERβ mRNA expression was only increased at 14 days with E treatment. These results demonstrate that E stimulates the colony forming potential of CD34(+) cells to a more megakaryocytic phenotype in vitro. This finding together with the stimulation of ER protein and mRNA expression adds to the increasing evidence for a role for MKs in estrogen‐induced bone formation. © 2004 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
A number of studies suggest that an inverse correlation exists between the epidermal growth factor-receptor and the estrogen receptor expression in primary human breast carcinoma as well as in established human breast carcinoma cell lines. Recent studies suggest that the epidermal growth factor-rece
## Abstract Estrogen receptor (ER)‐α can signal either via estrogen response element (ERE)‐mediated pathways or via alternate pathways involving protein–protein or membrane signaling. We previously demonstrated that, as compared to wild type (WT) controls, mice expressing a mutant ER‐α lacking the
## Abstract The present study was conducted to investigate the mRNA expression of the two estrogen receptor (ER) subtypes ERα and ERβ in the brain of Japanese quail embryos. We found expression of both ERα and ERβ mRNA in homogenate of whole head from 6‐day‐old embryos, and in brain homogenate from
## Abstract Ovaries from adult mice lacking both estrogen receptors ERα and ERβ (ERαβKO mice) contain abnormal cells sharing morphologic features with Sertoli cells, which are located mainly in the interstitial compartment. We show here that these cells express the Sertoli cell markers __TIF1β__, _