Target type: biologicalprocess
A homeostatic process involved in the maintenance of a steady state level of aspartate within a cell. [GOC:tb]
Intracellular aspartate homeostasis is a tightly regulated process that maintains the appropriate balance of aspartate within cells. Aspartate is a key metabolite involved in numerous cellular processes, including amino acid biosynthesis, the citric acid cycle, and the urea cycle. To ensure proper cellular function, aspartate levels must be tightly controlled, and this is achieved through a complex interplay of transport, synthesis, and degradation pathways.
**Aspartate Transport:**
* **Active transport:** Aspartate is transported into cells via specific membrane transporters, such as the glutamate-aspartate transporter (GLAST) and the aspartate transporter (AST). These transporters utilize energy to move aspartate against its concentration gradient, ensuring its accumulation inside the cell.
* **Passive diffusion:** Aspartate can also enter cells through passive diffusion, driven by its concentration gradient. This process is less efficient than active transport and is less relevant in maintaining overall aspartate homeostasis.
**Aspartate Synthesis:**
* **Transamination:** Aspartate is synthesized from oxaloacetate through the transamination reaction catalyzed by the enzyme aspartate aminotransferase (AST). This reaction involves the transfer of an amino group from glutamate to oxaloacetate, resulting in the formation of aspartate and α-ketoglutarate.
* **Other pathways:** Aspartate can also be synthesized through other pathways, such as the breakdown of purines and pyrimidines, but these are less significant contributors to overall aspartate homeostasis.
**Aspartate Degradation:**
* **Degradation to oxaloacetate:** Aspartate can be degraded back to oxaloacetate through the reverse reaction catalyzed by AST. This reaction is important for replenishing the citric acid cycle and for providing carbon skeletons for gluconeogenesis.
* **Urea cycle:** Aspartate is also a key component of the urea cycle, where it is used to remove excess nitrogen from the body. In this process, aspartate reacts with citrulline to form argininosuccinate, which is subsequently cleaved to form arginine and fumarate. The fumarate produced in this reaction can then enter the citric acid cycle.
**Regulation of Aspartate Homeostasis:**
* **Metabolic feedback:** The activity of the enzymes involved in aspartate synthesis and degradation is regulated by the cellular concentration of aspartate and other metabolites. For example, high aspartate levels can inhibit the activity of AST, while low aspartate levels can stimulate its activity.
* **Hormonal control:** Hormones such as insulin and glucagon can also influence aspartate homeostasis by regulating the activity of key enzymes and transporters.
* **Cellular signaling pathways:** Cellular signaling pathways, such as the mTOR pathway, can also modulate aspartate homeostasis by affecting the expression and activity of genes involved in aspartate metabolism.
**Significance of Aspartate Homeostasis:**
* **Essential for metabolic processes:** Proper aspartate homeostasis is essential for many metabolic processes, including amino acid biosynthesis, energy production, and nitrogen excretion.
* **Cell signaling and neurotransmission:** Aspartate is also involved in cell signaling and neurotransmission. It is an excitatory neurotransmitter in the brain and plays a role in learning and memory.
* **Disease implications:** Dysregulation of aspartate homeostasis can contribute to various diseases, such as cancer, diabetes, and neurodegenerative disorders.
In conclusion, intracellular aspartate homeostasis is a tightly regulated process that ensures the proper balance of aspartate within cells. This balance is critical for numerous metabolic processes, cell signaling, and overall cellular function. Understanding the mechanisms underlying aspartate homeostasis is important for developing strategies to treat diseases associated with its dysregulation.'
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Protein | Definition | Taxonomy |
---|---|---|
Acetyl-CoA carboxylase 2 | An acetyl-CoA carboxylase 2 that is encoded in the genome of human. [PRO:DNx, UniProtKB:O00763] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
cp-640186 | CP-640186: a potent inhibitor of mammalian Acetyl-coenzyme A carboxylases & can reduce body weight and improve insulin sensitivity in test animals; structure in first source | anthracenes; bipiperidines; morpholines; N-acylpiperidine | |
3,5-dichloro-2-hydroxy-N-(2-methoxy-5-phenylphenyl)benzenesulfonamide | biphenyls |