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. 2018 May 14;2018:9707543. doi: 10.1155/2018/9707543

Table 3.

Induction of gene expression in cultured RAW264.7 macrophages.

Gene name Functions Fold difference (treated versus untreated) P value (t-test, n = 3)
C4b Complement component 2.69 0.0155
Cxcl3 Chemokine ligand 3, a chemoattractant for neutrophils 8.45 0.0006
Il23a Interleukin 23 p19 for memory T cells −1.56 0.0276
Kng1 Suppressing tumor cell proliferation 13.56 0.0331
Lta (Tnfb) Lymphotoxin alpha, immunostimulation 2.89 0.0029
Nos2 Nitric oxide synthase 2, producing NO 9.71 0.0061
Tlr1 Toll-like receptor 1, recognizing pathogen-associated molecular patterns 2.55 0.0038
Tnf Tumor necrosis factor: inducing cell death 2.89 0.0081
Tnfsf14 TNF (ligand)superfamily, member 14, stimulating T cell proliferation and inducing cell death 2.99 0.0108

RAW264.7 macrophages were stimulated in the absence (untreated, culture medium only) or presence of 100 µg/mL of DI product in culture medium (treated) for 24 h. A panel of 84 genes related to “Inflammatory Response and Autoimmunity” was determined using PCR array. Data are presented as a list of gene expression that is statistically changed by extract treatment in four separate experiments.