The category of LYPD3 activators primarily contains chemical agents that function within crucial cellular pathways, casting an indirect influence on LYPD3's activity. A significant factor in understanding these activators is the insight into LYPD3's involvement in processes such as cell migration and adhesion. Chemicals like Retinoic Acid are instrumental in gene expression modulation, targeting genes within the axis of cell migration and adhesion. The resultant modulation, driven by Retinoic Acid, can alter the expression or functional landscape of LYPD3, effectively positioning it as an indirect activator.
Furthermore, the cellular energy regulation centerpoint, AMPK, becomes a focal pathway when considering LYPD3's association with cell migration. The activation of AMPK by agents like AICAR serves to shape the energy metabolism of the cell, and, in turn, processes that are energy-dependent, such as cell migration. This cascading influence can trickle down to proteins like LYPD3, making AICAR an indirect modulator. The recurring theme of cyclic nucleotides, particularly cAMP, is hard to ignore in the realm of cellular signaling. Chemicals like Rolipram and Dibutyryl-cAMP, which either elevate or mimic cAMP, steer several cellular signaling cascades. Such cascades, if intertwined with the functional domain of LYPD3, can be indirectly influenced by these chemicals. On similar lines, the intricate network of protein kinases, epitomized by PKC, serves as an avenue of LYPD3 modulation. Chemicals like PMA, which activate PKC, might regulate cellular events wherein LYPD3 plays a role, effectively marking PMA as an indirect LYPD3 activator.
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