Nal.pone.0055203.gpresent study confirms MMP-2 as a molecular target of

Nal.pone.0055203.gpresent study confirms MMP-2 as a molecular target of aeroplysinin-1 (Figure 1B). A second experimental approach to get more information on potential new molecular targets of aeroplysinin-1 has been the use of commercial low-density arrays of genes related with angiogenesis. In many published articles, authors make only an array experiment or a duplicate experiment, and in only a few published articles these experiments are independently repeated three or more times. Nonetheless, in the present study we only selected those modulatory effects that consistently were repeated in thewhole set 1531364 of five independent experiments. Among those genes fulfilling this strong requirement, the only two ones with decreases higher than 25 in their BIBS39 price 80-49-9 custom synthesis expression levels were TSP-1 and MCP1. Gene expression results obtained with gene arrays should be validated by using alternative, independent experimental approaches. Our results in the array experiments were confirmed by different, independent experimental approaches (Figure 2) showing that aeroplysinin-1 treatment down-regulates TSP-1 and MCP-1, two gene products involved in angiogenesis and also related to inflammation. TSP-1 has been described as anAeroplysinin-1 Inhibits Pro-Inflammatory MoleculesFigure 4. Aeroplysinin-1 abrogates the expression of PMA-induced COX-2 protein. A) PMA (50 ng/mL)-induced COX-2 mRNA was detected by qPCR, using the levels of amplification of GAPDH as a control. B) PMA (50 ng/mL)-induced COX-2 protein levels were detected by Western blotting as described, using the levels of b-actin as a control. C) The expression levels of the protein COX-2 were also analyzed in experiments carried out in the presence of cycloheximide (CHX), as shown in a Western blot. Cells were treated with cycloheximide (90 mg/mL) for 1 h. After washing both control and CHX-pretreated cells were treated in complete medium with PMA (50 ng/mL) in the presence or absence of aeroplysinin-1 (10 mM) for 4.5 h. D) The histogram shows the quantification of three independent experiments as that shown in C. doi:10.1371/journal.pone.0055203.gendogenous anti-angiogenic compound. However, TSP-1 is multifunctional, playing different biological activities in different cell types [21]. In fact, TSP-1 is one of the major proteins released from activated platelets [22]. Furthermore, TSP-1 expression is up-regulated in inflammation and inflammation-dependent pathologies, including atherosclerosis and coronary artery disease [22?4]. Very recently, it has been suggested that some of the pathophysiological connections of TSP-1 expression might be through its function as a hub in a mechanism for autocrine regulation of T cell adhesion and migration [24]. On the other hand, MCP-1 is a member of the C-C class of 24786787 the beta chemokine family with inflammatory properties [25]. MCP-1 up-regulation is related to macrophage recruitment, angiogenesis and survival in human breast cancer [26]. In addition, MCP-1 plays a critical role in the recruitment and activation of monocytes and in the development of atherosclerosis [27]. We have recently shown that another anti-angiogenic natural compound (namely, epigallocatechin 3-gallate) exerts also a potent inhibitory effect on MCP-1 in inflammatory cells [28,29]. In conclusion, the extreme selectivity of the conditions established in our experimental setup has been essential to identify two true positives as new molecular targets for the biological effects of aeroplysinin-1. Furt.Nal.pone.0055203.gpresent study confirms MMP-2 as a molecular target of aeroplysinin-1 (Figure 1B). A second experimental approach to get more information on potential new molecular targets of aeroplysinin-1 has been the use of commercial low-density arrays of genes related with angiogenesis. In many published articles, authors make only an array experiment or a duplicate experiment, and in only a few published articles these experiments are independently repeated three or more times. Nonetheless, in the present study we only selected those modulatory effects that consistently were repeated in thewhole set 1531364 of five independent experiments. Among those genes fulfilling this strong requirement, the only two ones with decreases higher than 25 in their expression levels were TSP-1 and MCP1. Gene expression results obtained with gene arrays should be validated by using alternative, independent experimental approaches. Our results in the array experiments were confirmed by different, independent experimental approaches (Figure 2) showing that aeroplysinin-1 treatment down-regulates TSP-1 and MCP-1, two gene products involved in angiogenesis and also related to inflammation. TSP-1 has been described as anAeroplysinin-1 Inhibits Pro-Inflammatory MoleculesFigure 4. Aeroplysinin-1 abrogates the expression of PMA-induced COX-2 protein. A) PMA (50 ng/mL)-induced COX-2 mRNA was detected by qPCR, using the levels of amplification of GAPDH as a control. B) PMA (50 ng/mL)-induced COX-2 protein levels were detected by Western blotting as described, using the levels of b-actin as a control. C) The expression levels of the protein COX-2 were also analyzed in experiments carried out in the presence of cycloheximide (CHX), as shown in a Western blot. Cells were treated with cycloheximide (90 mg/mL) for 1 h. After washing both control and CHX-pretreated cells were treated in complete medium with PMA (50 ng/mL) in the presence or absence of aeroplysinin-1 (10 mM) for 4.5 h. D) The histogram shows the quantification of three independent experiments as that shown in C. doi:10.1371/journal.pone.0055203.gendogenous anti-angiogenic compound. However, TSP-1 is multifunctional, playing different biological activities in different cell types [21]. In fact, TSP-1 is one of the major proteins released from activated platelets [22]. Furthermore, TSP-1 expression is up-regulated in inflammation and inflammation-dependent pathologies, including atherosclerosis and coronary artery disease [22?4]. Very recently, it has been suggested that some of the pathophysiological connections of TSP-1 expression might be through its function as a hub in a mechanism for autocrine regulation of T cell adhesion and migration [24]. On the other hand, MCP-1 is a member of the C-C class of 24786787 the beta chemokine family with inflammatory properties [25]. MCP-1 up-regulation is related to macrophage recruitment, angiogenesis and survival in human breast cancer [26]. In addition, MCP-1 plays a critical role in the recruitment and activation of monocytes and in the development of atherosclerosis [27]. We have recently shown that another anti-angiogenic natural compound (namely, epigallocatechin 3-gallate) exerts also a potent inhibitory effect on MCP-1 in inflammatory cells [28,29]. In conclusion, the extreme selectivity of the conditions established in our experimental setup has been essential to identify two true positives as new molecular targets for the biological effects of aeroplysinin-1. Furt.