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Electromagnetic Field-induced Stimulation of Bruton's Tyrosine Kinase
Here we present evidence that exposure of DT40 lymphoma B-cells to low energy electromagnetic fields (EMF) results in activation of phospholipase C-γ 2 (PLC-γ2), leading to increased inositol phospholipid turnover. PLC-γ2 activation in EMF-stimulated cells is mediated by stimulation of the Bruton...
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Published in: | The Journal of biological chemistry 1998-05, Vol.273 (20), p.12397-12401 |
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container_end_page | 12401 |
container_issue | 20 |
container_start_page | 12397 |
container_title | The Journal of biological chemistry |
container_volume | 273 |
creator | Kristupaitis, Daiva Dibirdik, Ilker Vassilev, Alexei Mahajan, Sandeep Kurosaki, Tomohiro Chu, Alice Tuel-Ahlgren, Lisa Tuong, Dong Pond, David Luben, Richard Uckun, Fatih M. |
description | Here we present evidence that exposure of DT40 lymphoma B-cells to low energy electromagnetic fields (EMF) results in activation of phospholipase C-γ 2 (PLC-γ2), leading to increased inositol phospholipid turnover. PLC-γ2 activation in EMF-stimulated cells is mediated by stimulation of the Bruton's tyrosine kinase (BTK), a member of the Src-related TEC family of protein tyrosine kinases, which acts downstream of LYN kinase and upstream of PLC-γ2. B-cells rendered BTK-deficient by targeted disruption of thebtk gene did not show enhanced PLC-γ2 activation in response to EMF exposure. Introduction of the wild-type (but not a kinase domain mutant) human btk gene into BTK-deficient B-cells restored their EMF responsiveness. Thus, BTK exerts a pivotal and mandatory function in initiation of EMF-induced signaling cascades in B-cells. |
doi_str_mv | 10.1074/jbc.273.20.12397 |
format | article |
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PLC-γ2 activation in EMF-stimulated cells is mediated by stimulation of the Bruton's tyrosine kinase (BTK), a member of the Src-related TEC family of protein tyrosine kinases, which acts downstream of LYN kinase and upstream of PLC-γ2. B-cells rendered BTK-deficient by targeted disruption of thebtk gene did not show enhanced PLC-γ2 activation in response to EMF exposure. Introduction of the wild-type (but not a kinase domain mutant) human btk gene into BTK-deficient B-cells restored their EMF responsiveness. Thus, BTK exerts a pivotal and mandatory function in initiation of EMF-induced signaling cascades in B-cells.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.273.20.12397</identifier><identifier>PMID: 9575194</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Agammaglobulinaemia Tyrosine Kinase ; Animals ; Chickens ; Electromagnetic Fields ; Enzyme Activation ; Isoenzymes - metabolism ; Lymphoma, B-Cell - enzymology ; Lymphoma, B-Cell - pathology ; Phospholipase C gamma ; Protein-Tyrosine Kinases - metabolism ; Tumor Cells, Cultured ; Type C Phospholipases - metabolism</subject><ispartof>The Journal of biological chemistry, 1998-05, Vol.273 (20), p.12397-12401</ispartof><rights>1998 © 1998 ASBMB. 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PLC-γ2 activation in EMF-stimulated cells is mediated by stimulation of the Bruton's tyrosine kinase (BTK), a member of the Src-related TEC family of protein tyrosine kinases, which acts downstream of LYN kinase and upstream of PLC-γ2. B-cells rendered BTK-deficient by targeted disruption of thebtk gene did not show enhanced PLC-γ2 activation in response to EMF exposure. Introduction of the wild-type (but not a kinase domain mutant) human btk gene into BTK-deficient B-cells restored their EMF responsiveness. Thus, BTK exerts a pivotal and mandatory function in initiation of EMF-induced signaling cascades in B-cells.</description><subject>Agammaglobulinaemia Tyrosine Kinase</subject><subject>Animals</subject><subject>Chickens</subject><subject>Electromagnetic Fields</subject><subject>Enzyme Activation</subject><subject>Isoenzymes - metabolism</subject><subject>Lymphoma, B-Cell - enzymology</subject><subject>Lymphoma, B-Cell - pathology</subject><subject>Phospholipase C gamma</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Type C Phospholipases - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLAzEQx4MotVbvXoQ96Wlr3rvrTUurYsGDFbyFbDIrKfuoya7Qb29KizdxLsPwf8D8ELokeEpwxm_XpZnSjE1pvCkrsiM0JjhnKRPk4xiNMaYkLajIT9FZCGschxdkhEaFyAQp-BjN5zWY3neN_myhdyZZOKht6lo7GLDJW--aoda969qkq5IHP_RdexOS1dZ3wbWQvLhWBzhHJ5WuA1wc9gS9L-ar2VO6fH18nt0vU8Mp7lMjCdiC51LqCnjGKyMZlTm2jHBBbcmM0IRZmZcVw1zgSmpJpMCUZVYICWyCrve9G999DRB61bhgoK51C90QVFbkUnBJ_jUSybmkTEYj3htNfCh4qNTGu0b7rSJY7RCriFhFxIrGe4c4Rq4O3UPZgP0NHJhG_W6vQyTx7cCrYBy0EafzkbWynfu7_AfOQ4m7</recordid><startdate>19980515</startdate><enddate>19980515</enddate><creator>Kristupaitis, Daiva</creator><creator>Dibirdik, Ilker</creator><creator>Vassilev, Alexei</creator><creator>Mahajan, Sandeep</creator><creator>Kurosaki, Tomohiro</creator><creator>Chu, Alice</creator><creator>Tuel-Ahlgren, Lisa</creator><creator>Tuong, Dong</creator><creator>Pond, David</creator><creator>Luben, Richard</creator><creator>Uckun, Fatih M.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19980515</creationdate><title>Electromagnetic Field-induced Stimulation of Bruton's Tyrosine Kinase</title><author>Kristupaitis, Daiva ; 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PLC-γ2 activation in EMF-stimulated cells is mediated by stimulation of the Bruton's tyrosine kinase (BTK), a member of the Src-related TEC family of protein tyrosine kinases, which acts downstream of LYN kinase and upstream of PLC-γ2. B-cells rendered BTK-deficient by targeted disruption of thebtk gene did not show enhanced PLC-γ2 activation in response to EMF exposure. Introduction of the wild-type (but not a kinase domain mutant) human btk gene into BTK-deficient B-cells restored their EMF responsiveness. Thus, BTK exerts a pivotal and mandatory function in initiation of EMF-induced signaling cascades in B-cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9575194</pmid><doi>10.1074/jbc.273.20.12397</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agammaglobulinaemia Tyrosine Kinase Animals Chickens Electromagnetic Fields Enzyme Activation Isoenzymes - metabolism Lymphoma, B-Cell - enzymology Lymphoma, B-Cell - pathology Phospholipase C gamma Protein-Tyrosine Kinases - metabolism Tumor Cells, Cultured Type C Phospholipases - metabolism |
title | Electromagnetic Field-induced Stimulation of Bruton's Tyrosine Kinase |
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