Fibroblast growth factors (FGF) are a family of cell signalling proteins produced by macrophages; they are involved in a wide variety of processes, most notably as crucial elements for normal development in animal cells. Any irregularities in their function lead to a range of developmental defects. These growth factors typically act as systemic or locally circulating molecules of extracellular origin that activate cell surface receptors. A defining property of FGFs is that they bind to heparin and to heparan sulfate. Thus, some are sequestered in the extracellular matrix of tissues that contains heparan sulfate proteoglycans and are released locally upon injury or tissue remodeling.
In humans, 23 members of the FGF family have been identified, all of which are structurally related signaling molecules:
Members FGF1 through FGF10 all bind fibroblast growth factor receptors (FGFRs). FGF1 is also known as acidic fibroblast growth factor, and FGF2 is also known as basic fibroblast growth factor.
Members FGF11, FGF12, FGF13, and FGF14, also known as FGF homologous factors 1-4 (FHF1-FHF4), have been shown to have distinct functions compared to the FGFs. Although these factors possess remarkably similar sequence homology, they do not bind FGFRs and are involved in intracellular processes unrelated to the FGFs. This group is also known as "iFGF".
Human FGF18 is involved in cell development and morphogenesis in various tissues including cartilage.
Human FGF20 was identified based on its homology to Xenopus FGF-20 (XFGF-20).
FGF15 through FGF23 were described later and functions are still being characterized. FGF15 is the mouse ortholog of human FGF19 (there is no human FGF15) and, where their functions are shared, they are often described as FGF15/19. In contrast to the local activity of the other FGFs, FGF15/19, FGF21 and FGF23 have hormonal systemic effects.
The mammalian fibroblast growth factor receptor family has 4 members, FGFR1, FGFR2, FGFR3, and FGFR4.
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This course provides a comprehensive overview of the biology of cancer, illustrating the mechanisms that cancer cells use to grow and disseminate at the expense of normal tissues and organs.
The course covers in detail molecular mechanisms of cancer development with emphasis on cell cycle control, genome stability, oncogenes and tumor suppressor genes.
Students will learn essentials of cell and developmental biology with an engineering mind set, with an emphasis on animal model systems and quantitative approaches.
This course will provide the fundamental knowledge in neuroscience required to
understand how the brain is organised and how function at multiple scales is
integrated to give rise to cognition and beh
This course will provide the fundamental knowledge in neuroscience required to
understand how the brain is organised and how function at multiple scales is
integrated to give rise to cognition and beh
This course will provide the fundamental knowledge in neuroscience required to
understand how the brain is organised and how function at multiple scales is
integrated to give rise to cognition and beh
Fibroblast growth factor 2, also known as basic fibroblast growth factor (bFGF) and FGF-β, is a growth factor and signaling protein encoded by the FGF2 gene. It binds to and exerts effects via specific fibroblast growth factor receptor (FGFR) proteins, themselves a family of closely related molecules. Fibroblast growth factor protein was first purified in 1975; soon thereafter three variants were isolated: 'basic FGF' (FGF2); Heparin-binding growth factor-2; and Endothelial cell growth factor-2.
Le facteur de croissance nerveuse ou NGF (acronyme de l'appellation anglophone Nerve growth factor) est un polypeptide de la famille des neurotrophines. Il est impliqué dans la croissance, la prolifération et la survie d'un certain nombre de neurones mais également d'autres cellules. Ce facteur de croissance a été le premier à avoir été identifié et à ce titre constitue le prototype de cette famille de facteurs. Son gène, NGF, est situé sur le chromosome 1 humain.
La neurogenèse désigne l'ensemble du processus de formation d'un neurone fonctionnel du système nerveux à partir d'une cellule souche neurale. Elle a principalement lieu lors du développement neuronal du cerveau chez l'embryon et l'enfant (« neurogenèse primaire »). Certaines structures cérébrales des mammifères continuent cependant à produire des neurones chez l'individu adulte (). Issues du neuroectoderme, provenant lui-même de l'ectoderme, ces cellules migrent pendant la formation des structures du système nerveux central (tube neural puis vésicules cérébrales primitives : prosencéphale, mésencéphale et rhombencéphale).
Couvre les structures des protéines, les fonctions cellulaires, le cytosquelette, l'ingénierie tissulaire et les ligands.
Explore les récepteurs nucléaires, la voie JAK-STAT, les facteurs de croissance, les perturbateurs endocriniens et les récepteurs aux œstrogènes.
Explore les mécanismes de signalisation cellulaire, y compris les récepteurs, les voies et la transduction du signal pour la régulation des gènes et les réponses cellulaires.
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