Figure 1.
Figure 1. Regulation of the expression of chemokine receptors CXCR1, CXCR3, and CXCR4 on purified CD56+CD16+ NK and CD56+CD3+ NK T cells. (A) (i) CD56+ cells were purified from peripheral blood lymphocytes. (ii) Three major subpopulations of CD56+ NK cells were found: CD56+CD3+CD16– NK T cells (35%), CD56+CD16+CD3– NK cells (60%), and CD56+CD16–CD3– NK cells (5%). (B) CD56+CD16+ NK cells, but not NK T cells, express CXCR1 (ii); after 48 hours' incubation with IL-2 (1000 IU/mL), the cell-surface expression of CXCR1 is down-regulated (iii). (C) CD56+CD3+ NK T cells, but not NK cells, express high levels of CXCR4 (ii); after 48 hours' incubation with IL-2, the cell-surface expression of CXCR4 is down-regulated on both types of cells (iii). (D) NK and NK T cells express low levels of CXCR3 (ii); after 48 hours' incubation with IL-2, the cell-surface expression of CXCR3 is up-regulated on both NK and NK T cells (iii). IgG2APE and IgG1PE were used as control antibodies (panels Bi, Ci, and Di).

Regulation of the expression of chemokine receptors CXCR1, CXCR3, and CXCR4 on purified CD56+CD16+ NK and CD56+CD3+ NK T cells. (A) (i) CD56+ cells were purified from peripheral blood lymphocytes. (ii) Three major subpopulations of CD56+ NK cells were found: CD56+CD3+CD16 NK T cells (35%), CD56+CD16+CD3 NK cells (60%), and CD56+CD16CD3 NK cells (5%). (B) CD56+CD16+ NK cells, but not NK T cells, express CXCR1 (ii); after 48 hours' incubation with IL-2 (1000 IU/mL), the cell-surface expression of CXCR1 is down-regulated (iii). (C) CD56+CD3+ NK T cells, but not NK cells, express high levels of CXCR4 (ii); after 48 hours' incubation with IL-2, the cell-surface expression of CXCR4 is down-regulated on both types of cells (iii). (D) NK and NK T cells express low levels of CXCR3 (ii); after 48 hours' incubation with IL-2, the cell-surface expression of CXCR3 is up-regulated on both NK and NK T cells (iii). IgG2APE and IgG1PE were used as control antibodies (panels Bi, Ci, and Di).

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