Date published: 2025-9-16

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HECA Activators

HECA, a crucial protein in lymphocyte trafficking and homing, is regulated by a series of chemical activators that influence its activity through various signaling pathways. Forskolin, through its activation of adenylate cyclase, elevates intracellular cAMP levels, subsequently enhancing PKA activity. This activation cascade indirectly promotes HECA's functional role in guiding lymphocytes to their targeted locations. Similarly, PMA and Ionomycin, by activating PKC and increasing intracellular calcium levels respectively, modulate signaling pathways that directly influence HECA's interactions with endothelial cells, crucial for lymphocyte adhesion and migration. Sphingosine-1-Phosphate, engaging with its receptors, initiates signaling that can further augment HECA's role in lymphocyte egress, an essential step in immune surveillance. Moreover, the phosphodiesterase 4 inhibitor Rolipram, by increasing cAMP levels, indirectly potentiates HECA's activity in the immune response.

Further refining the regulation of HECA are compounds that modulate specific signaling pathways. BAY 11-7082, an NF-κB inhibitor, alters inflammatory response pathways, thereby indirectly enhancing HECA's involvement in lymphocyte trafficking during inflammation. Similarly, SB203580 and U0126, inhibitors of p38 MAPK and MEK1/2 respectively, shift signaling dynamics in a manner that favors HECA's role in lymphocyte migration. The PI3K inhibitors LY294002 and Wortmannin, by altering PI3K-dependent pathways, contribute to the modulation of HECA's activity in lymphocyte adhesion and migration. The calcium ionophore A23187 further supports this regulation by increasing intracellular calcium, which is pivotal in activating pathways influencing HECA's function. Lastly, Staurosporine, despite its broad kinase inhibition spectrum, may indirectly enhance HECA's role by affecting specific kinases involved in lymphocyte adhesion and trafficking. Collectively, these activators orchestrate a complex regulatory network, fine-tuning HECA's pivotal role in the immune system.

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