Figure 5
Figure 5. Morphology of CpG DNA2006–activated CD27+ and CD27− B cells. Wright-Giemsa staining was used to demonstrate morphologic differences between the initial CD27+ and CD27− peripheral blood B cells as well as differentiation changes following each phase of the culture system for both populations. By the end of phase III, CD27+ and CD27− B cells had an identical plasmablast morphology. Results are representative of 4 independent experiments, each from a different blood donor. Images were photographed using a Nikon Labophot microscope (100×/1.17 numerical aperture oil objective) with a Nikon Coolpix digital camera using the manufacturer's software (Nikon, Melville, NY). JPEG images were viewed using Adobe Photoshop CS2 (Adobe Systems, San Jose, CA), and contrast adjustments were made.

Morphology of CpG DNA2006–activated CD27+ and CD27 B cells. Wright-Giemsa staining was used to demonstrate morphologic differences between the initial CD27+ and CD27 peripheral blood B cells as well as differentiation changes following each phase of the culture system for both populations. By the end of phase III, CD27+ and CD27 B cells had an identical plasmablast morphology. Results are representative of 4 independent experiments, each from a different blood donor. Images were photographed using a Nikon Labophot microscope (100×/1.17 numerical aperture oil objective) with a Nikon Coolpix digital camera using the manufacturer's software (Nikon, Melville, NY). JPEG images were viewed using Adobe Photoshop CS2 (Adobe Systems, San Jose, CA), and contrast adjustments were made.

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