Page last updated: 2024-10-24

cellular hypotonic salinity response

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 detection of, or exposure to, a decrease in the concentration of salt (particularly but not exclusively sodium and chloride ions) in the environment. [GOC:mah]

Cellular hypotonic salinity response is a complex process that involves multiple signaling pathways and cellular adaptations to maintain osmotic balance when exposed to a lower salt concentration (hypotonic) environment.

When a cell is exposed to a hypotonic environment, the water potential outside the cell becomes lower than that inside the cell. This leads to water influx into the cell, causing it to swell and potentially burst. To prevent this, cells employ various mechanisms to adapt and maintain their integrity:

**1. Sensing and Transducing the Hypotonic Stress:**

* **Osmoreceptors:** Cells possess specialized proteins (osmoreceptors) that detect the changes in osmotic pressure and initiate signaling pathways. These receptors can be located in the plasma membrane, cytoplasm, or nucleus.
* **Signaling Cascades:** Activated osmoreceptors trigger a cascade of signaling events. For example, the MAPK (mitogen-activated protein kinase) pathway is often involved in mediating the response to hypotonic stress.

**2. Cellular Adaptations:**

* **Water Channels (Aquaporins):** Cells regulate water movement through specialized protein channels called aquaporins. In hypotonic conditions, aquaporin activity can be regulated to control water influx.
* **Ion Transport:** The cell adjusts the concentration of ions, particularly potassium (K+) and sodium (Na+), across the plasma membrane to maintain osmotic balance. This involves activating ion pumps, channels, and transporters.
* **Organic Solute Accumulation:** Cells can accumulate organic solutes, such as amino acids, sugars, and glycerol, to increase their intracellular osmotic pressure and counteract the osmotic imbalance.
* **Volume Regulation:** To maintain cell volume, cells can activate mechanisms like the regulatory volume decrease (RVD) pathway, which involves the efflux of ions and organic solutes to reduce cell volume.

**3. Transcriptional and Post-Transcriptional Regulation:**

* **Gene Expression Changes:** The hypotonic stress response also involves changes in gene expression. Cells can upregulate the expression of genes involved in ion transport, water channel regulation, and stress response proteins.
* **Protein Modification:** Post-translational modifications like phosphorylation and ubiquitination can alter the activity of existing proteins, further fine-tuning the cellular response to hypotonic stress.

**Overall, the cellular hypotonic salinity response is a dynamic and multi-faceted process that involves sensing, signal transduction, and diverse cellular adaptations to maintain osmotic balance and cell integrity in a hypotonic environment.**'
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Proteins (2)

ProteinDefinitionTaxonomy
Transient receptor potential cation channel subfamily V member 4A transient receptor potential cation channel TRPV4 that is encoded in the genome of human. [PRO:CNA, UniProtKB:Q9HBA0]Homo sapiens (human)
Fructose-1,6-bisphosphatase 1A fructose-1,6-bisphosphatase 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P09467]Homo sapiens (human)

Compounds (32)

CompoundDefinitionClassesRoles
rtki cpdaromatic ether;
monochlorobenzenes;
quinazolines
antineoplastic agent;
antiviral agent;
epidermal growth factor receptor antagonist;
geroprotector
cannabinolCannabinol: A physiologically inactive constituent of Cannabis sativa L.dibenzopyran
disulfiramorganic disulfide;
organosulfur acaricide
angiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor;
EC 3.1.1.1 (carboxylesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
ferroptosis inducer;
fungicide;
NF-kappaB inhibitor
pd 1530354-((3-bromophenyl)amino)-6,7-dimethoxyquinazoline: structure given in first source

PD-153035 : A member of the class of quinazolines carrying a 3-bromophenylamino substituent at position 4 and two methoxy substituents at positions 6 and 7.
aromatic amine;
aromatic ether;
bromobenzenes;
quinazolines;
secondary amino compound
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
epidermal growth factor receptor antagonist
thiramthiram : An organic disulfide that results from the formal oxidative dimerisation of N,N-dimethyldithiocarbamic acid. It is widely used as a fungicidal seed treatment.

Thiram: A dithiocarbamate chemical, used commercially in the rubber processing industry and as a fungicide. In vivo studies indicate that it inactivates the enzyme GLUTATHIONE REDUCTASE. It has mutagenic activity and may induce chromosomal aberrations.
organic disulfideantibacterial drug;
antifungal agrochemical;
antiseptic drug
adenosine monophosphateAdenosine Monophosphate: Adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2'-, 3'-, or 5'-position.adenosine 5'-phosphate;
purine ribonucleoside 5'-monophosphate
adenosine A1 receptor agonist;
cofactor;
EC 3.1.3.1 (alkaline phosphatase) inhibitor;
EC 3.1.3.11 (fructose-bisphosphatase) inhibitor;
fundamental metabolite;
micronutrient;
nutraceutical
bis(1-piperidylthiocarbonyl)disulfidebis(1-piperidylthiocarbonyl)disulfide: indicator for analysis of copper; structure
monosulfirammonosulfiram: monosulfide derivative of disulfide DISULFIRAM; structureorganosulfur compound
dibenzothiazyl disulfidedibenzothiazol-2-yl disulfide : An organic disulfide resulting from the formal oxidative coupling of the thiol groups of two molecules of 1,3-benzothiazole-2-thiol. It is used as an accelerator in the rubber industry.

dibenzothiazyl disulfide: vulcanizing accelerant
benzothiazoles;
organic disulfide
allergen
diphenyl disulfidebenzenes
cannabichromene1-benzopyran
aica ribonucleotideAICA ribonucleotide : A 1-(phosphoribosyl)imidazolecarboxamide that is acadesine in which the hydroxy group at the 5' position has been converted to its monophosphate derivative.

AICA ribonucleotide: purine precursor that has antineoplastic activity
1-(phosphoribosyl)imidazolecarboxamide;
aminoimidazole
cardiovascular drug;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
plant metabolite;
Saccharomyces cerevisiae metabolite
(6ar-trans)-isomer of tetrahydrocannabivarin 9
dioxiramdioxiram: structure given in first source
mdl29,951
(+)-usnic acidusnic acid
1-(4-Methoxyphenyl)-2-nitroethylene4-methoxy-beta-nitrostyrene: has vasodilator activity; structure in first sourcemethoxybenzenes
hc 0300312-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)-N-(4-isopropylphenyl)acetamide: a TRPA1 channel blocker
1-phenyl-2-nitropropene1-phenyl-2-nitropropene: RN given refers to cpd without isomeric designation
hc-067047HC-067047: a TRPA1 antagonist; structure in first source
rn 1734RN 1734: a TRPV4 antagonist; structure in first source
herbacetinherbacetin : A pentahydroxyflavone that is kaempferol substituted by a hydroxy group at position 8. It is a natural flavonoid from flaxseed which exerts antioxidant, anti-inflammatory and anticancer activities.

herbacetin: from Ramose Scouring Rush Herb; structure in first source
7-hydroxyflavonol;
pentahydroxyflavone
angiogenesis inhibitor;
anti-inflammatory agent;
antilipemic drug;
antineoplastic agent;
apoptosis inducer;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
plant metabolite
gossypetingossypetin : A hexahydroxyflavone having the hydroxy groups placed at the 3-, 3'-, 4'-, 5- 7- and 8-positions.

gossypetin: inhibits activity of penicillinase enzyme in E coli
7-hydroxyflavonol;
hexahydroxyflavone
plant metabolite
baicaleintrihydroxyflavoneangiogenesis inhibitor;
anti-inflammatory agent;
antibacterial agent;
anticoronaviral agent;
antifungal agent;
antineoplastic agent;
antioxidant;
apoptosis inducer;
EC 1.13.11.31 (arachidonate 12-lipoxygenase) inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
ferroptosis inhibitor;
geroprotector;
hormone antagonist;
plant metabolite;
prostaglandin antagonist;
radical scavenger
scutellareinscutellarein : Flavone substituted with hydroxy groups at C-4', -5, -6 and -7.

scutellarein: aglycone of scutellarin from Scutellaria baicalensis; carthamidin is 2S isomer of scutellarein; do not confuse with isoscutellarein and/or isocarthamidin which are respective regioisomers, or with the scutelarin protein
tetrahydroxyflavonemetabolite
beta-nitrostyrenebeta-nitrostyrene: RN given refers to cpd without isomeric designation
cannabigerolcannabigerol : A member of the class of resorcinols that is resorcinol which is substituted by a (2E)-3,7-dimethylocta-2,6-dien-1-yl group at position 2 and by a pentyl group at position 5. It is a natural product found in Cannabis sativa and Helichrysum species.

cannabigerol: RN given refers to (E)-isomer; structure given in first source
phytocannabinoid;
resorcinols
anti-inflammatory agent;
antibacterial agent;
antioxidant;
appetite enhancer;
cannabinoid receptor agonist;
neuroprotective agent;
plant metabolite
n,n'-((5-(2-amino-5-(2-methylpropyl)-4-thiazolyl)-2-furanyl)phosphinylidene)bis(alanine) diethyl esterN,N'-((5-(2-amino-5-(2-methylpropyl)-4-thiazolyl)-2-furanyl)phosphinylidene)bis(alanine) diethyl ester: structure in first source
mb 05032
cannabidivarincannabidivarin: from Cannabis sativamonoterpenoid
N-(3-ethynylphenyl)-6,7-dimethoxy-4-quinazolinaminequinazolines
gsk 1016790aGSK1016790A : A tertiary carboxamide that is piperazine in which one of the amino groups has undergone condensation with the carboxy group of N-[(2,4-dichlorophenyl)sulfonyl]-L-serine, while the other has undergone condensation with the carboxy group of N-(1-benzothiophen-2-ylcarbonyl)-L-leucine. It is a cell-permeable, potent and selective agonist of the TRPV4 (transient receptor potential vanilloid 4) channel.1-benzothiophenes;
aromatic primary alcohol;
dichlorobenzene;
N-acylpiperazine;
sulfonamide;
tertiary carboxamide
TRPV4 agonist