6.9:
Internal Receptors
Internal receptors are soluble proteins that bind signaling molecules inside cells, either in the cytoplasm or nucleus, to trigger a response, such as a change in gene expression.
Typically, the ligands that bind to internal receptors are hydrophobic, non-polar molecules that diffuse through the plasma membrane of the targeted cells, or are compounds that may be synthesized intracellularly.
Once a ligand binds, a conformational change is induced in the receptor, which allows it to bind with other molecules in the cell.
For example, when the hormone testosterone, or its enzymatically converted form dihydrotestosterone, DHT, binds to an androgen receptor in the cytoplasm, the ligand-bound complex then undergoes structural changes, allowing it to move into the nucleus, dimerize, and expose a DNA-binding site, a region on the receptor that recognizes specific nucleotide sequences of DNA.
In this case, the areas of binding are called hormone, or androgen-response elements, which modulate the activity of certain genes, either promoting or blocking the synthesis of mRNAs to mediate androgen-specific effects in cells.
6.9:
Internal Receptors
Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
Similar to membrane-bound receptors, binding of a ligand to a receptor located in the cytoplasm or nucleus of a cell causes a conformational change in the receptor. Like transcription factors, the active receptor can bind to receptor-specific DNA binding sites to increase or decrease the transcription of target genes. In the case of an intracellular receptor located in the cytoplasm, the receptor-ligand complex must first cross the nuclear membrane.
Many steroid hormones, including estrogen and testosterone, use intracellular receptors to induce specific effects. As an example, estrogen can diffuse across the membrane; binding of estrogen to its receptor results in dimerization of the receptors and transport of the ligand-receptor complex to the nucleus. Once in the nucleus, the complex can bind to DNA sequences called Estrogen-Response Elements (EREs). Depending on the other transcription factors and co-activators, binding of activated estrogen receptors (ERs) to EREs may cause an increase or decrease in transcription of target genes.
The activation of other intracellular receptors, including some thyroid hormone receptors, requires that ligands cross both the plasma membrane and nuclear membrane, as the corresponding receptors reside in the nucleus. These ligand-receptor complexes then can bind to DNA, similar to the mechanism described above.
Suggested Reading
Murphy, Elizabeth. "Estrogen signaling and cardiovascular disease." Circulation Research 109, no. 6 (2011): 687-696. [Source]
Sever, Richard, and Christopher K. Glass. "Signaling by nuclear receptors." Cold Spring Harbor Perspectives in Biology 5, no. 3 (2013): a016709. [Source]
Azeem, Waqas, Margrete Reime Hellem, Jan Roger Olsen, Yaping Hua, Kristo Marvyin, Yi Qu, Biaoyang Lin, Xisong Ke, Anne Margrete Øyan, and Karl-Henning Kalland. "An androgen response element driven reporter assay for the detection of androgen receptor activity in prostate cells." PloS One 12, no. 6 (2017): e0177861. [Source]