Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4
The data described here is related to the research article titled (Gabl et al., 2016) [1]. Pepducins with peptide sequence derived from one of the intracellular domains of a given G-protein coupled receptor (GPCR) can either activate or inhibit cell functions. Here we include data on human neutrophi...
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doaj-06d48cf33d7047f3a4b47128e2885a982020-11-25T01:44:32ZengElsevierData in Brief2352-34092016-09-018411414Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4André Holdfeldt0Malene Winther1Michael Gabl2Claes Dahlgren3Huamei Forsman4Department of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, SwedenDepartment of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, SwedenDepartment of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, SwedenDepartment of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, SwedenCorresponding author: Tel.: +46 31 3424972; Mobile: +46 070 8701899.; Department of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, SwedenThe data described here is related to the research article titled (Gabl et al., 2016) [1]. Pepducins with peptide sequence derived from one of the intracellular domains of a given G-protein coupled receptor (GPCR) can either activate or inhibit cell functions. Here we include data on human neutrophil function induced by pepducins derived from β2AR (ICL3-8) and CXCR4 (ATI-2341), respectively. ICL3-8 exerts neither direct activating effect on the NADPH-oxidase as measured by superoxide release nor inhibitory effect on FPR signaling. ATI-2341 dose-dependently triggers neutrophil activation and these cells were subsequently desensitized in their response to FPR2 specific agonists F2Pal10 and WKYMVM. Moreover, the ATI-2341 response is inhibited by PBP10 and the peptidomimetic Pam-(Lys-betaNSpe)6-NH2 (both are FPR2 specific inhibitors), but not to the FPR1 specific inhibitor cyclosporine H.http://www.sciencedirect.com/science/article/pii/S2352340916303535 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
André Holdfeldt Malene Winther Michael Gabl Claes Dahlgren Huamei Forsman |
spellingShingle |
André Holdfeldt Malene Winther Michael Gabl Claes Dahlgren Huamei Forsman Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 Data in Brief |
author_facet |
André Holdfeldt Malene Winther Michael Gabl Claes Dahlgren Huamei Forsman |
author_sort |
André Holdfeldt |
title |
Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 |
title_short |
Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 |
title_full |
Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 |
title_fullStr |
Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 |
title_full_unstemmed |
Data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2AR and CXCR4 |
title_sort |
data on human neutrophil activation induced by pepducins with amino acid sequences derived from β2ar and cxcr4 |
publisher |
Elsevier |
series |
Data in Brief |
issn |
2352-3409 |
publishDate |
2016-09-01 |
description |
The data described here is related to the research article titled (Gabl et al., 2016) [1]. Pepducins with peptide sequence derived from one of the intracellular domains of a given G-protein coupled receptor (GPCR) can either activate or inhibit cell functions. Here we include data on human neutrophil function induced by pepducins derived from β2AR (ICL3-8) and CXCR4 (ATI-2341), respectively. ICL3-8 exerts neither direct activating effect on the NADPH-oxidase as measured by superoxide release nor inhibitory effect on FPR signaling. ATI-2341 dose-dependently triggers neutrophil activation and these cells were subsequently desensitized in their response to FPR2 specific agonists F2Pal10 and WKYMVM. Moreover, the ATI-2341 response is inhibited by PBP10 and the peptidomimetic Pam-(Lys-betaNSpe)6-NH2 (both are FPR2 specific inhibitors), but not to the FPR1 specific inhibitor cyclosporine H. |
url |
http://www.sciencedirect.com/science/article/pii/S2352340916303535 |
work_keys_str_mv |
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