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. 2016 Jan 21;10:371–381. doi: 10.2147/DDDT.S88193

Table 3.

Determination of B-lymphocyte proliferation by cytometry-based cell counting

Group PI (without polymyxin B) PI (with polymyxin B)
Control 1.08±0.005 1.08±0.005
LPS 1.59±0.026&& 1.19±0.02**,$$
EBNL 1.12±0.011&& 1.16±0.012**,$$
EBNM 1.15±0.01&& 1.19±0.012**,$$
EBNH 1.14±0.005&& 1.24±0.02**,$$

Notes: A total of 10 μg polymyxin B/mL and 10 μg LPS/mL or EBNE (0.19 mg/mL, 0.38 mg/mL, or 0.75 mg/mL) were dissolved in media and incubated with cells for 72 hours at 37°C with 5% CO2. Following incubation, the B lymphocytes were stained with anti-CD19 for 30 minutes at 37°C in darkness. The samples were analyzed by flow cytometry. The data are the mean ± SD (n=3/treatment).

&&

or

**

Significant difference from control group (P<0.01).

$$

The PI (with polymyxin B) significant difference from the PI (without polymyxin B) (P<0.01).

Abbreviations: LPS, lipopolysaccharide; EBNL, EBN low dose; EBNM, EBN medium dose; EBNH, EBN high dose; EBNE, EBN extract; PI, proliferation index; SD, standard deviation; EBN, Edible bird’s nest.