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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