| First Author | Fehniger TA | Year | 2007 |
| Journal | Immunity | Volume | 26 |
| Issue | 6 | Pages | 798-811 |
| PubMed ID | 17540585 | Mgi Jnum | J:123588 |
| Mgi Id | MGI:3718856 | Doi | 10.1016/j.immuni.2007.04.010 |
| Citation | Fehniger TA, et al. (2007) Acquisition of murine NK cell cytotoxicity requires the translation of a pre-existing pool of granzyme B and perforin mRNAs. Immunity 26(6):798-811 |
| abstractText | Although activated murine NK cells can use the granule exocytosis pathway to kill target cells immediately upon recognition, resting murine NK cells are minimally cytotoxic for unknown reasons. Here, we showed that resting NK cells contained abundant granzyme A, but little granzyme B or perforin; in contrast, the mRNAs for all three genes were abundant. Cytokine-induced in vitro activation of NK cells resulted in potent cytotoxicity associated with a dramatic increase in granzyme B and perforin, but only minimal changes in mRNA abundance for these genes. The same pattern of regulation was found in vivo with murine cytomegalovirus infection as a physiologic model of NK cell activation. These data suggest that resting murine NK cells are minimally cytotoxic because of a block in perforin and granzyme B mRNA translation that is released by NK cell activation. |
