Lack of effect of flurothyl, a non-anesthetic fluorinated ether, on rat brain synaptic plasma membrane calcium-atpase

Life Sciences ◽  
1999 ◽  
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pp. 179-183 ◽  
Author(s):  
J-L. Horn ◽  
P.K. Janicki ◽  
J.J. Franks
2010 ◽  
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Author(s):  
Katharine A. Kenyon ◽  
Eric A. Bushong ◽  
Amy S. Mauer ◽  
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Richard J. Weinberg ◽  
...  

2010 ◽  
Vol 518 (16) ◽  
pp. spc1-spc1
Author(s):  
Katharine A. Kenyon ◽  
Eric A. Bushong ◽  
Amy S. Mauer ◽  
Emanuel E. Strehler ◽  
Richard J. Weinberg ◽  
...  

1992 ◽  
Vol 136 (1) ◽  
pp. 123-126 ◽  
Author(s):  
Rick K. Yip ◽  
Mordecai P. Blaustein ◽  
Kenneth D. Philipson

2000 ◽  
Vol 32 (2-3) ◽  
pp. 100-105 ◽  
Author(s):  
Lijun Bian ◽  
Junwen Zeng ◽  
Douglas Borchman ◽  
Christopher A. Paterson

Heart ◽  
2014 ◽  
Vol 100 (Suppl 4) ◽  
pp. A17.1-A17
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RR Baggott ◽  
A Alfranca ◽  
MD López-Maderuelo ◽  
TMA Mohamed ◽  
A Escolano ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Maylin Merino-Wong ◽  
Barbara A. Niemeyer ◽  
Dalia Alansary

Immune responses involve mobilization of T cells within naïve and memory compartments. Tightly regulated Ca2+ levels are essential for balanced immune outcomes. How Ca2+ contributes to regulating compartment stoichiometry is unknown. Here, we show that plasma membrane Ca2+ ATPase 4 (PMCA4) is differentially expressed in human CD4+ T compartments yielding distinct store operated Ca2+ entry (SOCE) profiles. Modulation of PMCA4 yielded a more prominent increase of SOCE in memory than in naïve CD4+ T cell. Interestingly, downregulation of PMCA4 reduced the effector compartment fraction and led to accumulation of cells in the naïve compartment. In silico analysis and chromatin immunoprecipitation point towards Ying Yang 1 (YY1) as a transcription factor regulating PMCA4 expression. Analyses of PMCA and YY1 expression patterns following activation and of PMCA promoter activity following downregulation of YY1 highlight repressive role of YY1 on PMCA expression. Our findings show that PMCA4 adapts Ca2+ levels to cellular requirements during effector and quiescent phases and thereby represent a potential target to intervene with the outcome of the immune response.


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