Proplatelet formation of megakaryocytes is triggered by autocrine-synthesized estradiol

被引:84
作者
Nagata, Y
Yoshikawa, J
Hashimoto, A
Yamamoto, M
Payne, AH
Todokoro, K
机构
[1] RIKEN, Inst Phys & Chem Res, Cell Fate Signaling Res Unit, Wako, Saitama 3510198, Japan
[2] Univ Tsukuba, Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan
[3] Stanford Univ, Sch Med, Dept Obstet & Gynecol, Div Reprod Biol, Stanford, CA 94305 USA
关键词
sex steroid hormone; p45; NF-E2; proplatelet; 3; beta-HSD; hematopoiesis;
D O I
10.1101/gad.1128003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A matured megakaryocyte releases thousands of platelets through a drastic morphological change, proplatelet formation (PPF). The megakaryocyte/erythrocyte-specific transcription factor, p45 NF-E2, is essential for initiating PPF, but the factor regulating PPF has not been identified. Here we report that estradiol synthesized in megakaryocytes triggers PPF. We demonstrate that a key enzyme for steroid hormone biosynthesis, 3beta-hydroxysteroid dehydrogenase (3beta-HSD), is a target of p45 NF-E2, and rescues PPF of p45 NF-E2-deficient megakaryocytes. We also show that estradiol is synthesized within megakaryocytes, and that extracellular estradiol stimulates PPF, inhibition of 3beta-HSD activity blocks PPF, and estrogen receptor antagonists inhibit platelet production in vivo. We conclude that autocrine estradiol action regulates platelet production by triggering PPF.
引用
收藏
页码:2864 / 2869
页数:6
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