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Bruton's tyrosine kinase activity and inositol 1,4,5-trisphosphate production are not altered in DT40 lymphoma B cells exposed to power line frequency magnetic fields.

作者信息

Miller S C, Furniss M J

机构信息

Signal Transduction Laboratory, Pharmaceutical Discovery Division, SRI International, Menlo Park, California 94025, USA.

出版信息

J Biol Chem. 1998 Dec 4;273(49):32618-26. doi: 10.1074/jbc.273.49.32618.

DOI:10.1074/jbc.273.49.32618
PMID:9830001
Abstract

Exposure of wild-type DT40 lymphoma B cells or Bruton's tyrosine kinase (BTK)-deficient DT40 cells reconstituted with the human btk gene to a 1-gauss 60-Hz electromagnetic field (EMF) has been reported to rapidly increase inositol 1,4,5-trisphosphate (Ins 1,4, 5-P3) production (1,2). Here we have used BTK-deficient DT40 B cells reconstituted with the human btk gene to evaluate the reproducibility of these findings. An experimental design with blinded exposures and anti-IgM treatment to induce Ins 1,4,5-P3 production as a positive control, showed no significant effect of a 1-gauss 60-Hz EMF on Ins 1,4,5-P3 production. Because recent work has shown that the activation of BTK was required for EMF-responsiveness (2), we also evaluated the reproducibility of this finding in wild-type DT40 cells. BTK was activated in a dose- and time-dependent manner by treatment with the tyrosine phosphatase inhibitor pervanadate. However, the ability to detect BTK activation, as measured by increased autophosphorylation by immune complex kinase assay, was dependent on the kinase buffer. Using cells from the original investigators, no evidence was obtained to support the hypothesis that exposure to a 1-gauss 60-Hz EMF had a causal effect on protein-tyrosine kinase activities affecting Ins 1,4,5-P3 production.

摘要

相似文献

1
Bruton's tyrosine kinase activity and inositol 1,4,5-trisphosphate production are not altered in DT40 lymphoma B cells exposed to power line frequency magnetic fields.
J Biol Chem. 1998 Dec 4;273(49):32618-26. doi: 10.1074/jbc.273.49.32618.
2
Stimulation of Bruton's tyrosine kinase (BTK) and inositol 1,4,5-trisphosphate production in leukemia and lymphoma cells exposed to low energy electromagnetic fields.
Leuk Lymphoma. 2000 Dec;40(1-2):149-56. doi: 10.3109/10428190009054892.
3
Electromagnetic field-induced stimulation of Bruton's tyrosine kinase.电磁场诱导的布鲁顿酪氨酸激酶刺激
J Biol Chem. 1998 May 15;273(20):12397-401. doi: 10.1074/jbc.273.20.12397.
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Bruton's tyrosine kinase prevents activation of the anti-apoptotic transcription factor STAT3 and promotes apoptosis in neoplastic B-cells and B-cell precursors exposed to oxidative stress.布鲁顿酪氨酸激酶可阻止抗凋亡转录因子STAT3的激活,并促进暴露于氧化应激的肿瘤性B细胞和B细胞前体发生凋亡。
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5
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Stimulation of Src family protein-tyrosine kinases as a proximal and mandatory step for SYK kinase-dependent phospholipase Cgamma2 activation in lymphoma B cells exposed to low energy electromagnetic fields.在暴露于低能量电磁场的淋巴瘤B细胞中,Src家族蛋白酪氨酸激酶的激活是SYK激酶依赖性磷脂酶Cγ2激活的近端且必需步骤。
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7
BTK as a mediator of radiation-induced apoptosis in DT-40 lymphoma B cells.
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8
Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model.在X连锁无丙种球蛋白血症细胞模型中,自然发生的布鲁顿酪氨酸激酶突变无显性负效应。
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Bruton's tyrosine kinase as an inhibitor of the Fas/CD95 death-inducing signaling complex.布鲁顿酪氨酸激酶作为Fas/CD95死亡诱导信号复合物的抑制剂。
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10
Transcription factor STAT5A is a substrate of Bruton's tyrosine kinase in B cells.转录因子STAT5A是B细胞中布鲁顿酪氨酸激酶的底物。
J Biol Chem. 2001 Aug 17;276(33):31216-28. doi: 10.1074/jbc.M104874200. Epub 2001 Jun 18.

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