Abstract
Natural killer (NK) cells are involved not only in resistance to tumors and infection, but also in some transplantation reactions. A specific, inexpensive method for purifying large numbers of NK cells is often required. All NK cells in H-2 b mice express the surface marker NK1.1. We report a method for positively selecting NK1.1 + spleen cells from normal and Poly I:C-stimulated C56B1 6 mice using a magnetic cell separation technique known as MACS. Our results show that cytotoxic activity directed at YAC-1 target cells by normal and Poly I:C-stimulated spleen cells could be increased five-fold using this method. We also found that spleen cells from mice given Poly I:C could lyse NK-resistant, BW1100 target cells, and that this activity could be increased two-fold. Flow cytometry analysis of Poly I:C-stimulated, MACS enriched, NK1.1 + spleen cells revealed the presence of two subpopulations: one consisting of LGL and the other consisting of smaller, agranular lymphocytes (SAL). After enrichment, the percentage of NK1.1 + spleen cells increased from 69% to 91% in the LGL subpopulation and from 33% to 73% in the SAL subpopulation. These results clearly demonstrate the effectiveness of the MACS technique for purifying large numbers of NK1.1 + cells for both flow cytometric and functional analyses.
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