Estrogen stimulates differentiation of megakaryocytes and modulates their expression of estrogen receptors α and β

被引:24
|
作者
Bord, S [1 ]
Frith, E
Ireland, DC
Scott, MA
Craig, JIO
Compston, JE
机构
[1] Univ Cambridge, Addenbrookes Hosp, Sch Clin Med, Cambridge CB2 2QQ, England
[2] Addenbrookes Hosp, Dept Haematol, Cambridge CB2 2QQ, England
关键词
karyocytopoiesis; immunocytochemistry; ER alpha; ER beta; bone remodelling; estradiol; CD34(+); CD61; CD41;
D O I
10.1002/jcb.20035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 170 estradiol (E). Cells were immunolocalised for CD61, CD41, ERalpha and beta. 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 ERa expression at 6 days (P<0.001) whilst ERbeta was dose-dependently increased only at 9 days (P<0.01). ERalpha mRNA was increased at 6 days but not at 14 days whilst ERbeta 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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:249 / 257
页数:9
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