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Resolution: standard / high Figure 2.
Immunoglobulin secretion from CD3-CD38bright cells in bone marrow. (A) Fresh bone marrow-derived mononuclear cells (BMMCs) were stained with PerCP cyanin
5.5 dye for flow cytometric cell sorting (FL2H) according to immunoglobulin D (IgD)
phycoerythrin and CD38 expression, resulting in four populations: CD38low cells, IgD+CD38high cells, IgD-CD382+ cells and IgD-CD38bright cells. These cell populations were incubated on precoated ELISPOT plates as described
in the Methods section. (B) Using the enzyme-linked immunosorbent spot assay, we detected the number of spot-forming
units (SFUs) and quantified them for the IgG, IgM and IgA isotypes. PBS = phosphate-buffered
saline. Bars represent means ± SEM of five experiments. (C) Calculated total number of SFUs for total immunoglobulin (total Ig) secretion. (D) 2 × 2 table showing the sensitivity and specificity of the population of CD3-CD38bright cells to secrete immunoglobulins. The sensitivity was 92.9%, and the specificity was
53.6%. FACS = fluorescence-activated cell sorting.
Teng et al. Arthritis Research & Therapy 2012 14:R57 doi:10.1186/ar3770 |