Page last updated: 2024-10-24

cellular response to indole-3-methanol

Definition

Target type: biologicalprocess

Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an indole-3-methanol stimulus. [GOC:mah, GOC:yaf]

Indole-3-methanol (I3M), a naturally occurring compound found in cruciferous vegetables, elicits a complex cellular response by modulating multiple signaling pathways. I3M's biological activity is primarily attributed to its ability to activate aryl hydrocarbon receptor (AhR), a ligand-activated transcription factor. Upon binding to I3M, AhR translocates from the cytoplasm to the nucleus, where it forms a heterodimer with the aryl hydrocarbon receptor nuclear translocator (ARNT). This complex then binds to specific DNA sequences called dioxin response elements (DREs) in the promoter regions of target genes.

The activation of AhR by I3M leads to the transcriptional regulation of a diverse array of genes involved in various cellular processes, including xenobiotic metabolism, immune response, cell growth, and differentiation. For instance, I3M induces the expression of cytochrome P450 enzymes, such as CYP1A1 and CYP1B1, which are crucial for the detoxification of foreign compounds.

Furthermore, I3M's interaction with AhR can modulate the immune system. It has been shown to suppress inflammatory responses by inhibiting the production of pro-inflammatory cytokines, such as TNF-α and IL-6. Additionally, I3M can enhance the activity of natural killer (NK) cells, which play a role in eliminating infected or cancerous cells.

In terms of cell growth and differentiation, I3M exhibits a multifaceted role. It has been observed to promote cell proliferation in certain cell types, while simultaneously inhibiting the growth of others. This differential effect may be attributed to the context-dependent activation of downstream signaling pathways.

Beyond AhR activation, I3M has been shown to interact with other signaling pathways, including the nuclear factor erythroid 2-related factor 2 (Nrf2) pathway. Nrf2 is a transcription factor that plays a crucial role in protecting cells against oxidative stress. I3M's activation of Nrf2 leads to the upregulation of antioxidant genes, contributing to the overall protection of cells from damage.

In summary, the cellular response to I3M is a complex and multifaceted process involving the modulation of multiple signaling pathways. The activation of AhR and Nrf2 pathways plays a significant role in mediating I3M's effects on xenobiotic metabolism, immune response, cell growth, and differentiation. Further research is ongoing to fully elucidate the intricate mechanisms underlying I3M's biological activity and its potential therapeutic applications.'
"

Proteins (3)

ProteinDefinitionTaxonomy
Breast cancer type 1 susceptibility proteinA breast cancer type 1 susceptibility protein that is encoded in the genome of human. [PRO:DNx]Homo sapiens (human)
Catenin beta-1A catenin beta-1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P35222]Homo sapiens (human)
Cadherin-1A cadherin-1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P12830]Homo sapiens (human)

Compounds (7)

CompoundDefinitionClassesRoles
beta-thujaplicinbeta-thujaplicin : A monoterpenoid that is cyclohepta-2,4,6-trien-1-one substituted by a hydroxy group at position 2 and an isopropyl group at position 4. Isolated from Thuja plicata and Chamaecyparis obtusa, it exhibits antimicrobial activities.

beta-thujaplicin: structure
cyclic ketone;
enol;
monoterpenoid
antibacterial agent;
antifungal agent;
antineoplastic agent;
antiplasmodial drug;
plant metabolite
salvinsalvin: 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
toxoflavintoxoflavin : 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
cercosporincercosporin : 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-42773aromatic 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 ccalphostin C: structure given in first source; isolated from Cladosporium cladosporioides