Abstract:
:Activation of Jurkat T cells with phytohemagglutinin, CD3 or CD2 mAbs results in a marked inhibition of phosphatidylserine (PS) synthesis. Monitoring PS synthesis in T cells shows that: (i) after modulation of CD3 molecules the cells become refractory to further treatment with CD3 mAbs as well as to a further challenge with CD2 mAbs; and (ii) treatment of T cells with fluoride ions and cholera toxin, two known effectors of guanosine triphosphate-binding proteins, also resulted in a strong inhibition of the synthesis of this phospholipid. The inhibition of PS synthesis thus appears to be regulated similarly to the other activation events, suggesting that transmembrane signalling mechanisms leading to PS inhibition are the same as those previously proposed for increasing phosphatidylinositides turnover and subsequent rise in the intracellular calcium concn in lymphocytes.
journal_name
Mol Immunoljournal_title
Molecular immunologyauthors
Pelassy C,Dallanegra A,Aussel C,Fehlmann Mdoi
10.1016/0161-5890(89)90072-2subject
Has Abstractpub_date
1989-11-01 00:00:00pages
1081-6issue
11eissn
0161-5890issn
1872-9142journal_volume
26pub_type
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