Abstract

NK cell function in the rat is only defined in a rudimentary way due to missing tools for clear NK cell identification. The present study introduces the congenic LEW.BH-NKC rat strain which allows distinct detection of rat NK cells using commercial antibodies. LEW.BH-NKC rats were exposed in vivo to the porcine B cell line L23 by subcutaneous transfer of L23 cell suspension. We used Luciferase transgeneic L23 cells to follow the course of rejection by living imaging. L23 cells were rejected within five days after placement under the skin thus the rejection is mediated by innate immune responses in the first place. Indeed we found increased percentages of NK cells in the blood, spleen and in draining lymph nodes using flow cytometry methods. Surprisingly, we found as a consequence a decrease in proliferative T cell response in the draining lymph nodes. We identified NK cells as mediators of this regulation by in vitro performed mixed lymphocyte reactions. The remarkable feature was the naive state of NK cells exhibiting the regulative capacity. Furthermore, the regulation was not exclusively mediated by IL-10 as it has been reported before for influence of T cell response by activated NK cells but predominantly by TGF-β. Interestingly, after initiation of the adaptive immune response, NK cells failed to take influence on the proliferation of T cells. We conclude that naive NK cells build up a threshold of activation impulse that T cells have to overcome.

Highlights

  • Natural killer (NK) cells were identified in the 1970 as a nonphagocytic lymphocyte population with high cytotoxic potential which at first exclusively was correlated with antibody dependent cytotoxicity (ADCC) [1,2]

  • The staining of cells derived from Lewis wt rats using monoclonal antibody (mAb) 3.2.3 does not give specific information about NK cells since this common antibody cross-reacts with NKR-P1B which is expressed on monocytes (Fig. 1B)

  • A congenic rat strain was generated in our lab carrying the natural killer complex (NKC) of Black Hooded rats on Lewis rat background

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Summary

Introduction

Natural killer (NK) cells were identified in the 1970 as a nonphagocytic lymphocyte population with high cytotoxic potential which at first exclusively was correlated with antibody dependent cytotoxicity (ADCC) [1,2]. Due to the immediate response after direct engagement of activatory receptors, control of NK activation is crucial to prevent autoimmune response. This is guaranteed by constitutively expressed inhibitory receptors. In humans these receptors are assigned to the killer cell Ig-like receptors (KIR) and in rodents to the family of killer cell lectin-like receptors (KLR). The majority of these receptors interact with self-MHC I molecules and reveal cytoplasmatic immuno receptors tyrosine-based inhibitory motifs (ITIM) cells lacking self-MHC molecules are recognised as targets [4]

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