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PD-1 in human NK cells: evidence of cytoplasmic mRNA and protein expression.
Mariotti, Francesca R; Petrini, Stefania; Ingegnere, Tiziano; Tumino, Nicola; Besi, Francesca; Scordamaglia, Francesca; Munari, Enrico; Pesce, Silvia; Marcenaro, Emanuela; Moretta, Alessandro; Vacca, Paola; Moretta, Lorenzo.
Afiliação
  • Mariotti FR; Department of Immunology, IRCSS Bambino Gesù Children's Hospital, Rome, Italy.
  • Petrini S; Confocal Microscopy Core Facility, Research Center, IRCSS Bambino Gesù Children's Hospital, Rome, Italy.
  • Ingegnere T; Department of Immunology, IRCSS Bambino Gesù Children's Hospital, Rome, Italy.
  • Tumino N; Department of Immunology, IRCSS Bambino Gesù Children's Hospital, Rome, Italy.
  • Besi F; Department of Immunology, IRCSS Bambino Gesù Children's Hospital, Rome, Italy.
  • Scordamaglia F; Department of Pneumology, AO Villa Scassi, Genoa, Italy.
  • Munari E; Department of Pathology, Sacro Cuore Don Calabria Hospital, Negrar, Italy.
  • Pesce S; Department of Pathology AOUI, University of Verona, Verona, Italy.
  • Marcenaro E; Department of Experimental Medicine (DIMES), University of Genova, Genoa, Italy.
  • Moretta A; Department of Experimental Medicine (DIMES), University of Genova, Genoa, Italy.
  • Vacca P; Center of Excellence for Biomedical Research (CEBR), University of Genoa, Genoa, Italy.
  • Moretta L; Department of Experimental Medicine (DIMES), University of Genova, Genoa, Italy.
Oncoimmunology ; 8(3): 1557030, 2019.
Article em En | MEDLINE | ID: mdl-30723590
ABSTRACT
Under physiological conditions, PD-1/PD-L1 interactions regulate unwanted over-reactions of immune cells and contribute to maintain peripheral tolerance. However, in tumor microenvironment, this interaction may greatly compromise the immune-mediated anti-tumor activity. PD-1+ NK cells have been detected in high percentage in peripheral blood and ascitic fluid of ovarian carcinoma patients. To acquire information on PD-1 expression and physiology in human NK cells, we analyzed whether PD-1 mRNA and protein are present in resting, surface PD-1-, NK cells from healthy donors. Both different splicing isoforms of PD-1 mRNA and a cytoplasmic pool of PD-1 protein were detected. Similar results were obtained also from both in vitro-activated and tumor-associated NK cells. PD-1 mRNA and protein were higher in CD56dim than in CD56bright NK cells. Confocal microscopy analyses revealed that PD-1 protein is present in virtually all NK cells analyzed. The present findings are compatible with a rapid surface expression of PD-1 in NK cells in response to appropriate, still undefined, stimuli.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article