2008AFRICAN JOURNAL OF BIOTECHNOLOGYOpen access

Garcinia kola extract reduced lipopolysaccharide activation of macrophages using U937 cells as a model

Tebekeme Okoko, Ibiba F. Oruambo

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Abstract

The effect of Garcinia kola heckel seed extract on the promonocytic cell line U937 activated by lipopolysaccharide (LPS) was investigated. 200 l of U937 cells maintained in culture at 5 x 105 cells per ml was delivered into wells of a culture plate according to groups. Cells were pre-treated with 20 l of 100 ng/ml phorbol myristate acetate (PMA) for 24, 48, or 72 h in order to transform them to the macrophage form. Following the PMA treatment, some cells were incubated with 100 g/ml LPS (group C), while others (group D) were treated with 100 g/ml LPS and 100 il of 100 g/ml of the G. kola methanolic extract. Other cells (groups A, and B) were incubated with neither LPS nor extract. 24 h later, the supernatants were analysed for the production of TNF- and IL6 as indices for the activation of macrophages. The results show that the G. kola extract reduced the tendency of LPS to activate the cells. However, highest activation of LPS was observed when the cells were incubated with PMA for 48 h prior to the addition of LPS. This suggests that stimulation of U937 cells with PMA is necessary for the production of cytokines and that G. kola possesses considerable immunomodulatory activity.

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What this paper is about

The effect of Garcinia kola heckel seed extract on the promonocytic cell line U937 activated by lipopolysaccharide (LPS) was investigated. 200 l of U937 cells maintained in culture at 5 x 105 cells per ml was delivered into wells of a culture plate according to groups. Cells were pre-treated with 20 l of 100 ng/ml phorbol myristate acetate (PMA) for 24, 48, or 72 h in order to transform them to the macrophage form. Following the PMA treatment, some cells were incubated with 100 g/ml LPS (group C), while others (group D) were treated with 100 g/ml LPS and 100 il of 100 g/ml of the G. kola methanolic extract. Other cells (groups A, and B) were incubated with neither LPS nor extract. 24 h later, the supernatants were analysed for the production of TNF- and IL6 as indices for the activation of macrophages. The results show that the G. kola extract reduced the tendency of LPS to activate the cells. However, highest activation of LPS was observed when the cells were incubated with PMA for 48 h prior to the addition of LPS. This suggests that stimulation of U937 cells with PMA is necessary for the production of cytokines and that G. kola possesses considerable immunomodulatory activity.

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Available abstract

The effect of Garcinia kola heckel seed extract on the promonocytic cell line U937 activated by lipopolysaccharide (LPS) was investigated. 200 l of U937 cells maintained in culture at 5 x 105 cells per ml was delivered into wells of a culture plate according to groups. Cells were pre-treated with 20 l of 100 ng/ml phorbol myristate acetate (PMA) for 24, 48, or 72 h in order to transform them to the macrophage form. Following the PMA treatment, some cells were incubated with 100 g/ml LPS (group C), while others (group D) were treated with 100 g/ml LPS and 100 il of 100 g/ml of the G. kola methanolic extract. Other cells (groups A, and B) were incubated with neither LPS nor extract. 24 h later, the supernatants were analysed for the production of TNF- and IL6 as indices for the activation of macrophages. The results show that the G. kola extract reduced the tendency of LPS to activate the cells. However, highest activation of LPS was observed when the cells were incubated with PMA for 48 h prior to the addition of LPS. This suggests that stimulation of U937 cells with PMA is necessary for the production of cytokines and that G. kola possesses considerable immunomodulatory activity.

Key concepts: Lipopolysaccharide, Garcinia kola, U937 cell, Cell culture, Stimulation, Macrophage, Chemistry, THP1 cell line

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