Corticotropic cell
Corticotropic cell | |
---|---|
Details | |
Location | Anterior pituitary |
Function | Production of melanocyte-stimulating hormone, adrenocorticotropic hormone (ACTH) and lipotropin |
Identifiers | |
MeSH | D052680 |
TH | H3.08.02.2.00009 |
FMA | 83098 |
Anatomical terms of microanatomy |
Corticotropes (or corticotrophs) are
Function
The primary function of the corticotropic cells is to produce the
Hormone(s) | Main Targets | Effects |
---|---|---|
ACTH | Adrenal cortex | Glucocorticoid synthesis |
Skin Cells (Melanocytes), Brain, Exocrine Glands | Pigmentation of hair and skin, satiety, weight homeostasis[5] | |
CLIP | Pancreas | Insulin secretagogue, stimulates insulin release[6] |
γ-lipotropin
|
Adipose Tissue | Lipolysis, fatty acid mobilization[7] |
β-endorphin
|
Peripheral Nervous System | Pain management[8] |
Role in the Hypothalamic–pituitary–adrenal Axis
Stimulation
Corticotropic cells serve an important role within the feedback loop of the hypothalamic–pituitary–adrenal (HPA) axis and the stress response. Corticotropes produce and release ACTH, a 39 amino acid peptide hormone, in response to corticotropic releasing hormone (CRH) release from the hypothalamus. CRH is a 41-amino-acid peptide hormone that is secreted by the parvocellular neurosecretory cells, which are found within the paraventricular nucleus of the hypothalamus.[9]
Stimuli for the release of CRH from the hypothalamus include:
- Forskolin[10]
- Interleukin-6[10]
- Pituitary adenylate cyclase-activating peptide (PACAP)[10]
- Stress or trauma
- Circadian rhythms[5]
Forskolin and PACAP regulate the synthesis of CRH in the hypothalamus by binding to G protein-coupled receptors and stimulating and increase in cAMP within the cells via the action of adenylate cyclase. This activates the protein kinase A pathway, which results in the binding of cAMP response element binding protein (CREB) onto the CRH promoter region and induces transcription of CRH. This process is repressed by glucocorticoids; this inhibitory feedback helps maintain homeostasis of the stress response.[10]
Once released by the hypothalamus, CRH travels through the hypophyseal portal system to the anterior pituitary, where it binds to G protein-coupled receptors on the corticotropic cell membrane and stimulates cAMP production. The effects of CRH on pituitary corticotropes are potentiated by vasopressin (AVP); AVP is a weak inducer of ACTH production on its own, but has a strong synergistic effect on ACTH production when CRH is also bound to the receptor.[11] These signaling hormones act via signal transduction, causing the synthesis of POMC and eventual cleavage to ACTH and β-lipotropin. These peptide hormones are then released into the bloodstream, where they circulate and act on target tissues.
Function
ACTH released from the corticotropes binds to G protein-coupled receptors in the adrenal cortex, where it stimulates the production of glucocorticoids (primarily cortisol).[12] ACTH binds to the melanocortin 2 receptor and, through signal transduction, increases levels of cholesterol esterase, the transport of cholesterol across the mitochondrial membrane, cholesterol binding to P450SCC and, an increase in pregnenolone synthesis.[5] It also serves as a secondary stimulus for the synthesis of mineralocorticoids such as aldosterone, which serve an important role in regulating the salt balance of the blood.[13] Glucocorticoids released by the adrenal cortex inhibit production of CRH and ACTH, forming a negative feedback loop.[5]
Inhibition of ACTH production
Corticotropes contain
Associated diseases
Cushing's Disease
Corticotropic cells can have detrimental effects on the body if they express too much or too little ACTH. One such example is Cushing's disease, which can result from overproduction of ACTH in the corticotropes due to pituitary tumors known as corticotroph adenomas; this is the cause for roughly two-thirds of those diagnosed with Cushing's disease.[16] It is also possible that this disease can result from production of ACTH in a non-pituitary tumor, known as ectopic production, or the adrenal glands can overproduce cortisol due to an adrenal tumor.[17] This overproduction of ACTH causes an increase in cortisol levels due to increased glucocorticoid synthesis in the adrenal cortex resulting in several associated symptoms.
Symptoms of Cushing's disease include:
- Fatty deposits in the neck or back
- Stretch marks (striae)[18]
- Fatigue[18]
- Osteoporosis[18]
- Weakened immune system[18]
- Hypertension[18]
Addison's Disease
Corticotropic cells can also be the cause of Addison's disease in some instances. Addison's disease is characterized adrenal insufficiency, which is defined as the underproduction of glucocorticoids by the adrenal cortex. If the corticotropes underproduce ACTH this can result in secondary adrenal insufficiency, causing the adrenal glands to underproduce cortisol. This can be caused by tumors of the anterior pituitary or hypothalamus, inflammation, or surgery.[19] This ultimately results in the underproduction of cortisol, which has many detrimental symptoms.
Symptoms of Addison's disease include:
- Weight loss[20]
- Hypoglycemia[20]
- Hypotension[20]
- Irritability[20]
See also
- Neuroendocrinology
- Pituitary gland
- Somatotropic cell
- Lactotropic cell
- Somatomammotropic cell
- Gonadotropic cell
- Thyrotropic cell
- List of distinct cell types in the adult human body
References
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