Tenascin Activators encompass a selection of chemical compounds that indirectly promote Tenascin's activity by influencing various signaling pathways and cellular processes associated with the extracellular matrix (ECM). Forskolin, for instance, increases intracellular cAMP levels, subsequently activating protein kinase A (PKA), which can phosphorylate proteins involved in ECM remodeling, a process where Tenascin is a critical player. Similarly, Epigallocatechin gallate and Genistein, through their kinase inhibition, might shift the signaling equilibrium in such a way as to support Tenascin's role in ECM organization. Sphingosine-1-phosphate and Thapsigargin, by modulating lipid signaling and increasing intracellular calcium, respectively, can potentiate the cellular processes in which Tenascin is fundamentally involved, such as cell adhesion and migration. Moreover, PI3K inhibitors like LY294002 and Wortmannin could indirectly enhance Tenascin activity by impacting cellular survival pathways, potentially leading to ECM component upregulation.
The influence of Tenascin activators extends further through compounds that alter MAPK signaling. PD 98059, a MEK inhibitor, SB203580, a p38 MAPK inhibitor, and U0126, another MEK1/2 inhibitor, could all create conditions that favor Tenascin's contribution to ECM structure.
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