Target type: biologicalprocess
The cell fate determination process in which a cell becomes capable of differentiating autonomously into a glial cell regardless of its environment; upon determination, the cell fate cannot be reversed. [GOC:go_curators, GOC:mtg_sensu]
Glial cell fate determination is a complex and tightly regulated process that ensures the proper development and function of the nervous system. Glial cells, which provide structural support and metabolic sustenance to neurons, arise from glial progenitors, multipotent cells that can give rise to various glial subtypes. The fate decision of glial progenitors is influenced by a combination of intrinsic factors, such as gene expression and signaling pathways, and extrinsic cues from the microenvironment, including neuron-glia interactions and extracellular matrix components.
During development, glial progenitors undergo a series of molecular and morphological changes that lead to their differentiation into specific glial subtypes. This process involves the activation of specific transcription factors, signaling pathways, and epigenetic modifications that regulate the expression of genes required for glial cell identity and function.
One of the key transcription factors involved in glial cell fate determination is the bHLH factor Olig2. Olig2 is expressed in glial progenitors and plays a crucial role in promoting glial cell fate and suppressing neuronal fate. In the absence of Olig2, glial progenitors fail to differentiate into astrocytes and oligodendrocytes, and instead adopt a neuronal fate.
Another important signaling pathway involved in glial cell fate determination is the Notch signaling pathway. Notch signaling is activated by cell-cell interactions and leads to the activation of downstream target genes that regulate glial cell fate. For example, activation of Notch signaling in glial progenitors can promote oligodendrocyte differentiation and suppress astrocyte differentiation.
In addition to intrinsic factors, extrinsic cues from the microenvironment also play a critical role in glial cell fate determination. For example, neuron-glia interactions can influence glial cell fate by providing signals that promote the differentiation of specific glial subtypes. For example, neurons can release factors that promote astrocyte differentiation, such as TNFα and TGFβ.
The extracellular matrix, which surrounds glial progenitors and other cells in the nervous system, also provides cues that can influence glial cell fate. For example, the extracellular matrix component laminin has been shown to promote oligodendrocyte differentiation.
Overall, glial cell fate determination is a complex and dynamic process that involves the interplay of intrinsic and extrinsic factors. Understanding the molecular mechanisms underlying glial cell fate determination is essential for understanding the development and function of the nervous system and for developing therapies for glial cell disorders.'
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Protein | Definition | Taxonomy |
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Catenin beta-1 | A catenin beta-1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P35222] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
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salvin | salvin: a biocyclic diterpenoid; from sage and rosemary (Lamiaceae) | abietane diterpenoid; carbotricyclic compound; catechols; monocarboxylic acid | angiogenesis modulating agent; anti-inflammatory agent; antineoplastic agent; antioxidant; apoptosis inducer; food preservative; HIV protease inhibitor; plant metabolite |
toxoflavin | toxoflavin : A pyrimidotriazine that is 1,6-dimethyl-1,5,6,7-tetrahydropyrimido[5,4-e][1,2,4]triazine with oxo groups at positions 5 and 7. toxoflavin: azapteridine antibiotic; structure | carbonyl compound; pyrimidotriazine | antibacterial agent; antineoplastic agent; apoptosis inducer; bacterial metabolite; toxin; virulence factor; Wnt signalling inhibitor |
cercosporin | cercosporin : An organic heterohexacyclic compound that is perylo[1,12-def][1,3]dioxepine-6,11-dione substituted by hydroxy groups at positions 5 and 12, by methoxy groups at positions 7 and 10, and by 2-hydroxypropyl groups at positions 8 and 9 (the R,R-stereoisomer). It is a phytotoxin which was first isolated from the pathogenic soybean fungus, Cercospora kikuchii and later found in multiple members of the genus Cercospora. cercosporin: phyytotoxin from Cercospora beticola Sacc; posses photodynamic action on mice, bacteria & plants | ||
LSM-42773 | aromatic ketone | ||
etodolac, (-)-isomer | (R)-etodolac : The R-enantiomer of etodolac. It is inactive, in contrast to the enantiomer, (S)-etodolac, which is a preferential inhibitor of cyclo-oxygenase 2 and a non-steroidal anti-inflammatory. The racemate is commonly used for the treatment of rheumatoid arthritis and osteoarthritis, and for the alleviation of postoperative pain. | etodolac | |
ucn 1028 c | calphostin C: structure given in first source; isolated from Cladosporium cladosporioides |