SLC10A4, a member of the solute carrier family 10, plays a pivotal role in the cellular uptake of various compounds, including bile acids, steroids, and thyroid hormones. As a transmembrane transporter, SLC10A4 is essential for maintaining cellular homeostasis and regulating metabolic processes through the transport of substrates across the cell membrane. Functionally, SLC10A4 is involved in bile acid recycling, steroid hormone signaling, and thyroid hormone metabolism, highlighting its significance in diverse physiological functions.
Activation of SLC10A4 is intricately regulated by various cellular signaling pathways and molecular mechanisms. One prominent mode of activation involves the modulation of gene expression through epigenetic modifications, such as histone acetylation and deacetylation. Compounds like sodium butyrate, retinoic acid, and curcumin activate SLC10A4 by promoting histone acetylation, leading to enhanced transcription of the SLC10A4 gene and increased transporter expression and activity. Additionally, certain agents, such as forskolin and sulforaphane, activate SLC10A4 by stimulating specific signaling pathways, such as the cAMP-PKA pathway and the Nrf2-mediated antioxidant response, respectively, resulting in the upregulation of transporter function. Overall, the activation of SLC10A4 is a tightly regulated process involving multiple cellular pathways and molecular mechanisms, ensuring proper substrate transport and cellular function.
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