The vitamin D receptor-mediated activation of phosphatidylinositol 3-kinase (PI3Kα) plays a role in the 1α,25-dihydroxyvitamin D3-stimulated increase in steroid sulphatase activity in myeloid leukaemic cell lines

被引:26
作者
Hughes, Philip J. [1 ]
Lee, Jimmy S. [2 ]
Reiner, Neil E. [2 ]
Brown, Geoffrey [1 ]
机构
[1] Univ Birmingham, Div Immun & Infect, Sch Med, Birmingham B15 2TT, W Midlands, England
[2] Univ British Columbia, Dept Med, Div Infect Dis, Fac Med & Sci,Vancouver Coastal Hlth Res Inst, Vancouver, BC V5Z 3J5, Canada
关键词
vitamin D receptor; phosphatidlylinositol; 3-kinase; genomic and non-genomic signalling; steroid sulphatase; myeloid cells;
D O I
10.1002/jcb.21545
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
In this article we show that 1 alpha,25-dihydroxyvitamin D-3 (1 alpha,25(OH)(2)D-3) stimulates the activity of the class IA phosphatidylinositol 3-kinase PI3K alpha and its downstream target Akt in HL60, U937 and THP-1 myeloid leukaemic cell lines. Furthermore, we show that the classical nuclear vitamin D receptor (VDRnuc) is involved in this activation of the PI3K/Akt signalling in these cell lines. We have previously shown that the activity of steroid sulphatase is stimulated in HL60, U937 and THP-1 myeloid leukaemic cell lines by 1 alpha,25(OH)(2)D-3 (Hughes et al., [2001] Biochem J 355:361 -371; Hughes et al. [2005] J Cell Biochem 94:1175-1189; Hughes and Brown [2006] J Cell Biochem 98:590-617). In this article we show that the 1 alpha,25(OH)(2)D-3-stimulated increase in signalling via the PI3K/Akt pathway plays a role in the increase in steroid sulphatase activity in the HL60 U937 and THP-1 cell lines. We used a variety of pharmacological and biochemical approaches to show that activation of PI3K alpha mediates the 1 alpha,25(OH)(2)D-3-stimulated increase in steroid sulphatase activity in myeloid leukaemic cells. We also show that the PI3K/Akt dependent activation of NF-kappa B plays a role in the 1 alpha,25(OH)(2)D-3-stimulated increase in steroid sulphatase activity in myeloid leukaemic cells.
引用
收藏
页码:1551 / 1572
页数:22
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