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Up-regulation of DNAM-1 and NKp30, associated with improvement of NK cells activation after long-term culture of mononuclear cells from patients with ovarian neoplasia
Authors:Rodrigo Fernandes da Silva,Carlos Alberto Petta,Sophie Franç  oise Derchain,Evren Alici,Fernando Guimarã  es
Affiliation:1. Hospital da Mulher Professor Doutor José Aristodemo Pinotti – Centro de Atenção Integral à Saúde da Mulher, University of Campinas (UNICAMP), Campinas, Brazil;2. Departamento de Tocoginecologia, Faculdade de Ciências Médicas, University of Campinas (UNICAMP), Campinas, Brazil;3. Cell and Gene Therapy, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Huddinge, Stockholm, Sweden
Abstract:
This study aimed at evaluating the functional activation and activating receptors expression on resting, short- and long-term NK and NK-like T cells from blood of ovarian neoplasia patients. Blood from patients with adnexal benign alterations (n = 10) and ovarian cancer (grade I–IV n = 14) were collected after signed consent. Effector cells activation was evaluated by the expression of the CD107a molecule. Short-term culture was conducted overnight with IL-2 and long-term culture for 21 days, by a method designed to expand CD56+ lymphocytes. Short-term culture significantly increased NK cells activation compared to resting NK cells (p < 0.05), however, the long-term procedure supported an even higher increase (p < 0.001). Resting NK-like T cells showed poor activation, which was not altered by the culture procedures. The long-term culture effectively increased the expression of the activating receptors on NK and NK-like T cells, either by increasing the number of cells expressing a given receptor and/or by up-regulating their expression intensity. As a conclusion, the long-term culture system employed, resulted in a high number of functional NK cells. The culture system was particularly efficient on the up-regulation of NKp30 and DNAM-1 receptors on NK cells.
Keywords:NK-like T lymphocytes   NCRs (natural cytotoxic receptors)   CD107a   Degranulation   Regulatory T cells
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