Fibroblast Growth Factor 17 (FGF-17) is a member of the fibroblast growth factor family, a group of structurally related proteins that are broad-spectrum modulators of cell proliferation and differentiation. FGF-17 in particular has been the subject of interest for its role in the development of the nervous system, where it is involved in the proliferation and differentiation of cells within the central nervous system, as well as in limb development. The expression of FGF-17 is tightly controlled and occurs in specific patterns during embryonic development, indicating its critical function in proper morphogenesis and organogenesis. The protein operates by binding to FGF receptors, which activate a cascade of downstream signaling pathways that govern developmental processes, cell survival, and growth.
The regulation of FGF-17 expression can be influenced by a diverse array of chemical compounds, known as activators, which can upregulate or stimulate the production of this growth factor. These activators can induce the expression of FGF-17 through various mechanisms, such as initiating transcriptional changes, activating signaling pathways, and modifying epigenetic marks. For instance, compounds like retinoic acid and Vitamin D3 interact with their respective receptors to stimulate the expression of genes during development, including FGF-17. Other molecules, such as forskolin, work by elevating intracellular signaling molecules like cAMP, subsequently activating protein kinases that lead to the expression of target genes. Histone deacetylase inhibitors like trichostatin A and sodium butyrate can alter chromatin structure, facilitating transcriptional activators to enhance gene expression, including that of FGF-17. Moreover, hormonal molecules, such as estrogens and triiodothyronine, bind to their specific hormone receptors, influencing gene expression patterns in a manner that can lead to the upregulation of FGF-17. While the interplay between these activators and the expression of FGF-17 is an ongoing area of study, it is clear that the precise control of FGF-17 levels is a complex process involving multiple regulatory factors.
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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 may upregulate FGF-17 by binding to retinoic acid receptors, initiating transcriptional changes in developmental genes. | ||||||
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $71.00 $163.00 $296.00 | 2 | |
Active metabolites of Cholecalciferol can stimulate FGF-17 expression by engaging vitamin D receptors that elevate gene transcription in target cells. | ||||||
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 can induce FGF-17 expression by raising intracellular cAMP, which in turn activates protein kinase A (PKA) and other downstream effectors involved in gene transcription. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Dexamethasone may stimulate FGF-17 expression via glucocorticoid receptor-mediated activation of specific transcription factors. | ||||||
Lithium | 7439-93-2 | sc-252954 | 50 g | $214.00 | ||
Lithium chloride can upregulate FGF-17 by activating the Wnt/β-catenin signaling pathway, which plays a crucial role in gene transcription linked to development and growth. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $63.00 $182.00 | 8 | |
β-Estradiol can stimulate FGF-17 transcription by binding to estrogen receptors, which interact with estrogen response elements on the FGF-17 gene promoter. | ||||||
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 may increase FGF-17 expression by inhibiting histone deacetylases, thereby allowing transcriptional activators greater access to DNA. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine can induce FGF-17 expression by demethylating DNA and removing epigenetic silencing marks, facilitating gene activation. | ||||||
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 may stimulate the expression of FGF-17 by inhibiting histone deacetylases, leading to a more relaxed chromatin state and active gene transcription. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $28.00 $38.00 | 5 | |
Isoproterenol can upregulate FGF-17 expression through β-adrenergic receptors, activating cAMP-dependent pathways that culminate in increased gene transcription. | ||||||