MSP-1 Activators are thought to exert their effects through the modulation of intracellular signaling pathways. Forskolin and isoproterenol act to elevate cAMP levels, triggering PKA activation. Since PKA mediates phosphorylation events that can modify protein activity, these compounds might enhance MSP-1 activation as PKA phosphorylation is involved in its regulation. Anisomycin and TPA are known to activate JNK/SAPK and PKC pathways, respectively, which could lead to the activation of MSP-1 through stress and inflammatory response pathways or through direct phosphorylation as MSP-1 is a PKC substrate.
The increase in intracellular calcium by ionomycin and A23187 can act on various calcium-dependent signaling molecules, potentially including MSP-1 as it is responsive to calcium signaling. The use of cAMP analogs such as 8-Br-cAMP and db-cAMP can mimic the effect of cAMP elevation, directly activating cAMP-dependent pathways and potentially affecting the activation status of MSP-1. Epinephrine, as a physiological activator of adrenergic receptors, can also stimulate cAMP production and activate these pathways. Thapsigargin's role in manipulating calcium signaling can influence numerous calcium-dependent proteins and pathways, with potential effects on MSP-1. Lastly, retinoic acid modulates gene expression and could affect MSP-1.
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