ITF-1, identified as a pivotal transcription factor, plays a fundamental role in the orchestration of gene expression during various biological processes, including the development of the immune system. The protein functions as a transcriptional regulator, possessing the ability to bind to specific DNA sequences, thereby facilitating the transcription of downstream genes. ITF-1's expression is subject to precise regulation within cellular environments, as it is integral to maintaining the balance of cellular proliferation, differentiation, and function. In the complex network of intracellular signaling, ITF-1 acts as a node that integrates signals from various pathways, translating them into gene expression outcomes that are crucial for cell fate decisions. Research into the mechanisms governing ITF-1 expression has unveiled a multitude of molecular actors capable of inducing its expression, which, in turn, can have substantial effects on the cellular transcriptome.
Among the array of molecules identified to potentially induce the expression of ITF-1, retinoic acid emerges as a significant player. As a derivative of vitamin A, retinoic acid engages with its nuclear receptors to initiate a transcriptional cascade, which can result in the upregulation of ITF-1. Another influential molecule, Vitamin D3, upon its conversion to the biologically active form, has been shown to interact with its specific nuclear receptors, potentially leading to the stimulation of ITF-1 expression. Additionally, compounds such as forskolin, which increases intracellular cAMP levels, activate a cascade involving the cAMP response element-binding protein (CREB) that may culminate in elevated ITF-1 transcription. Furthermore, epigenetic modifiers like trichostatin A and sodium butyrate, which inhibit histone deacetylase activity, create a more open chromatin structure, potentially facilitating increased ITF-1 gene transcription. The diversity in the mechanisms of these molecules highlights the intricate web of regulation that controls the expression of ITF-1, reflecting the complexity of cellular homeostasis and the fine-tuned genetic responses to internal and external stimuli.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $66.00 $325.00 $587.00 $1018.00 | 28 | |
Retinoic acid can initiate transcriptional activation by binding to retinoic acid receptors, which may upregulate ITF-1 expression during processes such as hematopoietic differentiation. | ||||||
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $71.00 $163.00 $296.00 | 2 | |
Upon hydroxylation, Cholecalciferol becomes active and can stimulate the expression of ITF-1 by engaging the vitamin D receptor, notably within immune cell lineages. | ||||||
Cyclosporin A | 59865-13-3 | sc-3503 sc-3503-CW sc-3503A sc-3503B sc-3503C sc-3503D | 100 mg 100 mg 500 mg 10 g 25 g 100 g | $63.00 $92.00 $250.00 $485.00 $1035.00 $2141.00 | 69 | |
Cyclosporin A inhibits calcineurin, preventing the dephosphorylation and activation of the nuclear factor of activated T-cells (NFAT), which can lead to an increase in ITF-1 expression in T-cell lineages. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $41.00 $132.00 $214.00 $500.00 $948.00 | 119 | |
Phorbol esters, like PMA, by mimicking diacylglycerol, activate protein kinase C (PKC) and can stimulate ITF-1 expression through PKC-mediated signaling pathways that lead to transcriptional activation. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Forskolin elevates intracellular cAMP levels, thereby activating protein kinase A (PKA) which can induce the expression of ITF-1 as part of the cAMP response element-binding (CREB) protein signaling pathway. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $43.00 $73.00 $126.00 $243.00 $530.00 $1259.00 | 11 | |
Epigallocatechin Gallate has antioxidant properties and can stimulate the expression of ITF-1 potentially through the activation of Nrf2-dependent antioxidant response element (ARE) signaling pathways. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Dexamethasone binds to glucocorticoid receptors, which can translocate to the nucleus and upregulate ITF-1 expression as part of the immune response modulation and apoptosis in lymphocytes. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride inhibits glycogen synthase kinase-3 (GSK-3), which can lead to the stabilization and nuclear accumulation of β-catenin, a co-activator for lymphoid enhancer-binding factor 1 (LEF1); this pathway can induce ITF-1 expression in cells involved in immune regulation. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
Trichostatin A, as a histone deacetylase inhibitor, can lead to the acetylation of histones, reducing chromatin compaction and allowing greater access for transcriptional machinery, thus potentially increasing the transcription of ITF-1. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium butyrate also acts as a histone deacetylase inhibitor, enhancing histone acetylation and promoting a transcriptionally active chromatin state that may induce higher levels of ITF-1 transcription. | ||||||