Figure 2
Figure 2. Modulation of chemokine receptor expression by sHLA-G on NK cells from tonsil. Cytofluorimetric analysis of chemokine receptor expression on purified total NK cells from tonsil, gating on CD56bright or CD56dim NK cells on the basis of CD56 expression. (A) Representative staining with anti-CD56 mAb. The expression of chemokine receptors was evaluated on CD56bright (B) and CD56dim (C) NK cells, either untreated (black bars) or treated with sHLA-G (white bars). Data are expressed as MRFI. Means of 5 different experiments ± SD are shown. Asterisks indicate significant differences. The insets in panels B and C show representative stainings of NK cells, ctr, or treated with sHLA-G, with anti-CXCR3 and anti-CXCR5 mAbs. Black profiles indicate staining with specific mAbs, whereas gray profiles indicate staining with irrelevant isotype-matched mAb.

Modulation of chemokine receptor expression by sHLA-G on NK cells from tonsil. Cytofluorimetric analysis of chemokine receptor expression on purified total NK cells from tonsil, gating on CD56bright or CD56dim NK cells on the basis of CD56 expression. (A) Representative staining with anti-CD56 mAb. The expression of chemokine receptors was evaluated on CD56bright (B) and CD56dim (C) NK cells, either untreated (black bars) or treated with sHLA-G (white bars). Data are expressed as MRFI. Means of 5 different experiments ± SD are shown. Asterisks indicate significant differences. The insets in panels B and C show representative stainings of NK cells, ctr, or treated with sHLA-G, with anti-CXCR3 and anti-CXCR5 mAbs. Black profiles indicate staining with specific mAbs, whereas gray profiles indicate staining with irrelevant isotype-matched mAb.

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