Fig. 6.
Fig. 6. Morphologic and phenotypical characterization of the C2174PBL cells. / (A,B) C2174PBL cell line cytospins after 20 months of culture; note the presence of multinucleated giant cells (Giemsa staining). Original magnification of each, × 40. (C) An aliquot of the C2174PBL cultured PBMCs permeabilized and then stained with rabbit specific antibodies (CD3 FITC, CD8 FITC) and EBV-LMP1 antibody (LMP1 PE) was fixed in paraformaldehyde placed in mounting media and analyzed using a Leica DMRA microscope (using program QFISH). Original magnification, × 63. The upper portion of panel C shows a double-positive cell for LMP1 and CD3. The dent present on the upper right corner clearly shows evidence of an adjacent double-negative cell. The middle panel shows an LMP1-positive and a CD8−cell, whereas the lower panel shows a CD3+ and an LMP1-negative cell. (D) Histogram plots from the FACS analysis of the C2174 cultured PBMCs at 20 months of culture. Blue lines indicate specific isotypic control.

Morphologic and phenotypical characterization of the C2174PBL cells.

(A,B) C2174PBL cell line cytospins after 20 months of culture; note the presence of multinucleated giant cells (Giemsa staining). Original magnification of each, × 40. (C) An aliquot of the C2174PBL cultured PBMCs permeabilized and then stained with rabbit specific antibodies (CD3 FITC, CD8 FITC) and EBV-LMP1 antibody (LMP1 PE) was fixed in paraformaldehyde placed in mounting media and analyzed using a Leica DMRA microscope (using program QFISH). Original magnification, × 63. The upper portion of panel C shows a double-positive cell for LMP1 and CD3. The dent present on the upper right corner clearly shows evidence of an adjacent double-negative cell. The middle panel shows an LMP1-positive and a CD8cell, whereas the lower panel shows a CD3+ and an LMP1-negative cell. (D) Histogram plots from the FACS analysis of the C2174 cultured PBMCs at 20 months of culture. Blue lines indicate specific isotypic control.

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