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

被引:25
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
相关论文
共 34 条
[1]  
ARMITAGE P, 1994, STAT INFERENCE
[2]   Megakaryocyte population in human bone marrow increases with estrogen treatment: A role in bone remodeling? [J].
Bord, S ;
Vedi, S ;
Beavan, SR ;
Horner, A ;
Compston, JE .
BONE, 2000, 27 (03) :397-401
[3]  
Bord S, 2002, BONE, V30, P651
[4]   Mechanisms by which high-dose estrogen therapy produces anabolic skeletal effects in postmenopausal women: Role of locally produced growth factors [J].
Bord, S ;
Beavan, S ;
Ireland, D ;
Horner, A ;
Compston, JE .
BONE, 2001, 29 (03) :216-222
[5]   Estrogen receptors α and β are differentially expressed in developing human bone [J].
Bord, S ;
Horner, A ;
Beavan, S ;
Compston, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (05) :2309-2314
[6]   Localization of estrogen receptor β protein expression in adult human bone [J].
Braidman, IP ;
Hainey, L ;
Batra, G ;
Selby, PL ;
Saunders, PTK ;
Hoyland, JA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (02) :214-220
[7]   Molecular basis of agonism and antagonism in the oestrogen receptor [J].
Brzozowski, AM ;
Pike, ACW ;
Dauter, Z ;
Hubbard, RE ;
Bonn, T ;
Engstrom, O ;
Ohman, L ;
Greene, GL ;
Gustafsson, JA ;
Carlquist, M .
NATURE, 1997, 389 (6652) :753-758
[8]  
CARTER JM, 1991, MED LAB SCI, V48, P134
[9]  
Cheng LZ, 2000, J CELL PHYSIOL, V184, P58, DOI 10.1002/(SICI)1097-4652(200007)184:1<58::AID-JCP6>3.0.CO
[10]  
2-B