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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002703naa a2200277 4500
001oai:DiVA.org:liu-81990
003SwePub
008120927s2006 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-819902 URI
024a https://doi.org/10.1074/jbc.M6013472002 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Gasser, Andreasu University Medical Center Hamburg-Eppendorf, Germany4 aut
2451 0a Second Messenger Function of Nicotinic Acid Adenine Dinucleotide Phosphate Revealed by an Improved Enzymatic Cycling Assay
264 1b American Society for Biochemistry and Molecular Biology,c 2006
338 a print2 rdacarrier
520 a Nicotinic acid adenine dinucleotide phosphate (NAADP) is the most potent activator of Ca2+ release from intracellular stores known today. Although recent reports have suggested an important function of NAADP in human T lymphocytes, direct evidence for receptor-induced formation of NAADP is yet missing in these cells. Thus, we developed a highly sensitive and specific enzyme assay capable of quantifying low fmol amounts of NAADP. In unstimulated T cells, the NAADP concentration amounted to 4.4 +/- 1.6 nm (0.055 +/- 0.028 pmol/mg of protein). Stimulation of the cells via the T cell receptor/CD3 complex resulted in biphasic elevation kinetics of cellular NAADP levels and was characterized by a bell-shaped concentration-response curve for NAADP. In contrast, the NAADP concentration was elevated neither upon activation of the ADP-ribose/TRPM2 channel Ca2+ signaling system nor by an increase of the intracellular Ca2+ concentration upon thapsigargin stimulation. T cell receptor/CD3 complex-mediated NAADP formation was dependent on the activity of tyrosine kinases because genistein completely blocked NAADP elevation. Thus, we propose a regulated formation of NAADP upon specific stimulation of the T cell receptor/CD3 complex, suggesting a function of NAADP as a Ca2+-mobilizing second messenger during T cell activation.
700a Bruhn, Sören,d 1976-u University Medical Center Hamburg-Eppendorf, Germany4 aut0 (Swepub:liu)sorbr27
700a Guse, Andreasu University Medical Center Hamburg-Eppendorf, Germany4 aut
710a University Medical Center Hamburg-Eppendorf, Germany4 org
773t Journal of Biological Chemistryd : American Society for Biochemistry and Molecular Biologyg 281:25, s. 16906-16913q 281:25<16906-16913x 0021-9258x 1083-351X
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-81990
8564 8u https://doi.org/10.1074/jbc.M601347200

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