Details

Autor(en) / Beteiligte

• Prinz, Daniela
• Klein, Klara
• List, Julia
• Knab, Vanessa M.
• Menzl, Ingeborg
• Leidenfrost, Nicoletta
• Heller, Gerwin
• Polić, Bojan
• Putz, Eva Maria
• Witalisz‐Siepracka, Agnieszka
• Sexl, Veronika
• Gotthardt, Dagmar

Titel

Loss of NKG2D in murine NK cells leads to increased perforin production upon long‐term stimulation with IL‐2

Ist Teil von

• European journal of immunology, 2020-06, Vol.50 (6), p.880-890

Ort / Verlag

Germany: Wiley Subscription Services, Inc

Erscheinungsjahr

2020

Link zum Volltext

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• NK cells are innate lymphocytes responsible for lysis of pathogen‐infected and transformed cells. One of the major activating receptors required for target cell recognition is the NK group 2D (NKG2D) receptor. Numerous reports show the necessity of NKG2D for effective tumor immune surveillance. Further studies identified NKG2D as a key element allowing tumor immune escape. We here use a mouse model with restricted deletion of NKG2D in mature NKp46+ cells (NKG2DΔNK). NKG2DΔNK NK cells develop normally, have an unaltered IFN‐γ production but kill tumor cell lines expressing NKG2D ligands (NKG2DLs) less efficiently. However, upon long‐term stimulation with IL‐2, NKG2D‐deficient NK cells show increased levels of the lytic molecule perforin. Thus, our findings demonstrate a dual function of NKG2D for NK cell cytotoxicity; while NKG2D is a crucial trigger for cytotoxicity of tumor cells expressing activating ligands it is also capable to limit perforin production in IL‐2 activated NK cells. NKG2D has a dual function in NK cell cytotoxicity; while NKG2D is a crucial trigger for cytotoxicity against tumor cells expressing activating ligands, it limits perforin production in IL‐2 activated NK cells. The increased perforin levels are not linked to an altered activation of the JAK/STAT pathway.