TY - JOUR
T1 - O30 Natural compounds affecting neutrophil migration
T2 - The 5th International Conference on the Mechanism of Action of Nutraceuticals
AU - Morad, Hassan
AU - Luqman, Suaib
AU - McNaughton, Peter
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Hydrogen peroxide (H2O2) has recently been identified as the earliest messenger released by damaged tissues and is crucial for the chemoattraction of neutrophils to sites of injury and infection. However, how neutrophils sense and respond to H2O2 remains unresolved. Recently, we have identified the transient potential receptor melastatin-2 ion channel (TRPM2) as having a key role in directing the chemotaxis of neutrophils towards hydrogen peroxide (H2O2), in both in vitro and in vivo models. We isolated neutrophils from wild-type and TRPM2−/− mice and we observed that the genetic deletion of TRPM2 results in a reduction in both the speed and directionality of the neutrophil migration up a gradient of H2O2. We tested a diverse group of natural products, including a range of terpenes, alkaloids and flavonoids, for their effects on this H2O2-induced neutrophil chemotaxis using the Ibidi-chemotaxis system, which allows live-cell imaging in vitro of migration over time. From our screen, we have identified: beta-carotene, artemisinin, ferulic acid and N-acetylcysteine as compounds which reduce neutrophil chemotaxis in a comparable way to TRPM2 deletion, leading to the suggestion that they may be acting as TRPM2 inhibitors. Moreover, our compounds induce a more pronounced reduction in chemotaxis than the currently available TRPM2 inhibitors, which lack potency and selectivity. The natural compounds we have tested may have clinical applications; for example, in the treatment of inflammatory conditions, such as sepsis, which are characterised by excessive and damaging neutrophil migration.
AB - Hydrogen peroxide (H2O2) has recently been identified as the earliest messenger released by damaged tissues and is crucial for the chemoattraction of neutrophils to sites of injury and infection. However, how neutrophils sense and respond to H2O2 remains unresolved. Recently, we have identified the transient potential receptor melastatin-2 ion channel (TRPM2) as having a key role in directing the chemotaxis of neutrophils towards hydrogen peroxide (H2O2), in both in vitro and in vivo models. We isolated neutrophils from wild-type and TRPM2−/− mice and we observed that the genetic deletion of TRPM2 results in a reduction in both the speed and directionality of the neutrophil migration up a gradient of H2O2. We tested a diverse group of natural products, including a range of terpenes, alkaloids and flavonoids, for their effects on this H2O2-induced neutrophil chemotaxis using the Ibidi-chemotaxis system, which allows live-cell imaging in vitro of migration over time. From our screen, we have identified: beta-carotene, artemisinin, ferulic acid and N-acetylcysteine as compounds which reduce neutrophil chemotaxis in a comparable way to TRPM2 deletion, leading to the suggestion that they may be acting as TRPM2 inhibitors. Moreover, our compounds induce a more pronounced reduction in chemotaxis than the currently available TRPM2 inhibitors, which lack potency and selectivity. The natural compounds we have tested may have clinical applications; for example, in the treatment of inflammatory conditions, such as sepsis, which are characterised by excessive and damaging neutrophil migration.
U2 - 10.1016/j.bcp.2017.06.095
DO - 10.1016/j.bcp.2017.06.095
M3 - Meeting abstract
SN - 0006-2952
VL - 139
SP - 119
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
ER -