IndietroCell Signaling: Steroid Hormones and G Protein-Coupled Receptors
Guida di studio - Note intelligenti
Appunti personalizzati basati sui tuoi materiali, ampliati con definizioni chiave, esempi e contesto.
Cell Signaling Mechanisms
Steroid Hormone Signaling: Cortisol and Intracellular Receptors
Steroid hormones such as cortisol are lipid-soluble molecules that can cross the plasma membrane and interact with intracellular receptors. This process leads to changes in gene expression within the target cell.
Cortisol passes through the plasma membrane into the cytoplasm.
Steroid hormones are hydrophobic and can diffuse through the lipid bilayer of the cell membrane.
Cortisol binds to an intracellular receptor in the cytoplasm.
This forms a cortisol-receptor complex.
Cortisol-receptor complex enters the nucleus where it binds to specific genes.
The complex acts as a transcription factor, regulating gene expression.
Cortisol-receptor complex acts as a transcription factor.
It binds to DNA at specific response elements, promoting or inhibiting transcription of target genes.
The transcribed mRNA is translated into a specific protein.
This leads to the physiological effects associated with cortisol.
Example: Cortisol regulates metabolism by increasing the transcription of genes involved in gluconeogenesis in liver cells.
Step | Description |
|---|---|
1 | Cortisol passes through the plasma membrane into the cytoplasm. |
2 | Cortisol binds to an intracellular receptor, forming a cortisol-receptor complex. |
3 | Cortisol-receptor complex enters the nucleus and binds to DNA. |
4 | Cortisol-receptor complex acts as a transcription factor. |
5 | Transcription of target genes produces mRNA, which is translated into protein. |
Additional info: Steps such as "Cortisol binds to a receptor on the outside of the cell" and "Cortisol-receptor complex forms in the cytoplasm" are not applicable to steroid hormone signaling, as these hormones use intracellular, not cell-surface, receptors.
G Protein-Coupled Receptor (GPCR) Signaling: Histamine and the H1 Receptor
Histamine is a chemical messenger involved in inflammatory and allergic responses. It exerts its effects by binding to specific cell-surface receptors, such as the H1 receptor, which is a type of G protein-coupled receptor (GPCR).
Histamine binds extracellularly to the H1 receptor.
The H1 receptor is located on the plasma membrane of target cells.
Upon binding, the H1 receptor undergoes a conformational change and binds intracellularly to an inactive G protein, activating it.
This activation involves the exchange of GDP for GTP on the G protein.
The active G protein binds to the enzyme phospholipase C, activating it.
Phospholipase C then catalyzes the production of second messengers (e.g., IP3 and DAG), leading to cellular responses such as increased calcium release.
Histamine is highly hydrophilic.
As a result, it cannot cross the plasma membrane and must bind to cell-surface receptors.
Example: In allergic reactions, histamine released from mast cells binds to H1 receptors on smooth muscle cells, causing contraction and symptoms such as bronchoconstriction.
Step | Description |
|---|---|
1 | Histamine binds extracellularly to the H1 receptor. |
2 | H1 receptor activates an intracellular G protein. |
3 | Active G protein activates phospholipase C. |
4 | Phospholipase C generates second messengers, leading to a cellular response. |
Additional info: GPCR signaling is a common mechanism for transmitting signals from hydrophilic ligands that cannot cross the plasma membrane.