Cargando…

PD-1 in human NK cells: evidence of cytoplasmic mRNA and protein expression

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 de...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350684/
https://www.ncbi.nlm.nih.gov/pubmed/30723590
http://dx.doi.org/10.1080/2162402X.2018.1557030
Descripción
Sumario: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 CD56(dim) than in CD56(bright) 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.