Natural killer (NK) cells play a key role in inflammation and tumor regression through their ability to migrate into tissues. The two major subsets in NK cells are CD56
bright CD16
dim/- and CD56
dim CD16
+. The cytotoxic activity of CD56
dim NK cells is significantly greater than that of CD56
bright cells. Regarding cytokine production, the situation is inverted. CD56
bright NK cells are the most efficient cytokine producers. The role of CD56
bright CD16
- cells is not clear. CXCL12 is a chemokine that promotes Iymphocyte invasion and migration into tissues; however, the mechanism for this process remains incompletely understood. This study demonstrated that the NK92 cell population, which is the human NK cell line, was CD56
bright CD16
-. We examined the production of pro-matrix metalloproteinase (MMP) 1 induced by CXCL12 stimulation on NK92 cells. Pro-MMP 1 production was significantly enhanced by CXCL12 stimulation. In addition, the production of pro-MMP 1 was markedly inhibited by SB203580 (p38 inhibitor). These results suggest that p38, which is the family of mitogen activated protein kinases (MAPKs), was involved in the production of pro-MMP 1 from CXCL12-stimulated CD56
bright CD16
- NK92 cells.
View full abstract