Biogenesis of G-protein mediated calcium signaling in human megakaryocytes

被引:0
|
作者
den Dekker, E
Gorter, G
van der Vuurst, H
Heemskerk, JWM
Akkerman, JWN
机构
[1] Univ Utrecht, Med Ctr, Dept Haematol, Lab Thrombosis & Haemostasis, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Biomembrane Inst, NL-3584 CX Utrecht, Netherlands
[3] Maastricht Univ, Dept Biochem, Maastricht, Netherlands
[4] Maastricht Univ, Dept Human Biol, Maastricht, Netherlands
关键词
megakaryocytopoiesis; signaling; trimeric G-proteins; calcium;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To understand how platelet signal transduction pathways develop during megakaryocytopoiesis, we isolated human stem cells from umbilical cord blood and cultured the cells in the presence of thrombopoietin (TPO). Based on the early expression of CD61 and late expression of CD42b, immature (CD61(+)/CD42b(low)) and mature (CD61(+)/CD42b(high)) megakaryocytes were immunomagnetically purified and, together with stem cells (CD34(+)), characterized for G alpha-protein expression and agonist-induced [Ca2+](i), increases. Megakaryocytopoiesis was accompanied by down-regulation of the 43 kDa and 46 kDa variants of G(16)alpha, constant expression of G(s)alpha, and up-regulation of G(q)alpha and G(i)alpha1/2. The increase in G(q)alpha and G(i)alpha1/2 expression was accompanied by an increase in Ca2+ signaling triggered by thrombin and other agonists known to signal to Ca2+ via these G-proteins in platelets. The prostacyclin analog iloprost and TPO also induced [Ca2+](i), increases, and the iloprost-induced Ca2+ response disappeared during maturation. These data reveal sharp changes in Ca2+ regulation during megakaryocytopoiesis.
引用
收藏
页码:1106 / 1113
页数:8
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