Chromaffin cell

Chromaffin cells, also called pheochromocytes (or phaeochromocytes), are neuroendocrine cells found mostly in the medulla of the adrenal glands in mammals. These cells serve a variety of functions such as serving as a response to stress, monitoring carbon dioxide and oxygen concentrations in the body, maintenance of respiration and the regulation of blood pressure.[1] They are in close proximity to pre-synaptic sympathetic ganglia of the sympathetic nervous system, with which they communicate, and structurally they are similar to post-synaptic sympathetic neurons. In order to activate chromaffin cells, the splanchnic nerve of the sympathetic nervous system releases acetylcholine, which then binds to nicotinic acetylcholine receptors on the adrenal medulla. This causes the release of catecholamines. The chromaffin cells release catecholamines: ~80% of adrenaline (epinephrine) and ~20% of noradrenaline (norepinephrine) into systemic circulation for systemic effects on multiple organs (similarly to secretory neurones of the hypothalamus), and can also send paracrine signals. Hence they are called neuroendocrine cells.

Medullary chromaffin cell
Adrenal gland. (Medulla labeled at bottom right.)
Details
LocationMedulla adrenal gland
Identifiers
Latinendocrinocytus medullaris
MeSHD019439
THH3.08.02.6.00015
FMA69263
Anatomical terms of microanatomy

Structure

There are two types of cells that originate from the neural crest and are related to the sympathetic nervous system (originate from a cell called sympathogonia):[2]

1) Neuroblasts: These cells migrate, during the fourth to the fifth week of fetal development in humans, on both sides of the spinal cord toward the region just behind the dorsal aorta forming the two chains of sympathetic ganglia (Sympathetic chain). From these ganglia, the post synaptic sympathetic fibers will arise and extend toward their target organ. Some of these cells will migrate to the adrenal medulla to form sympathetic ganglia cells within the adrenal medulla (without postsynaptic sympathetic fibers). A tumor arising from these cells is called neuroblastoma.[3]

2) Chromaffin cells (or pheochromocytes): These cells will migrate to the area adjacent to the sympathetic ganglia (hence the name paraganglia) and to the adrenal medulla where they will be the most abundant type of cells. The largest extra-adrenal cluster of chromaffin cells in mammals is the organ of Zuckerkandl.[4] Tumors arising from these cell are called paragangliomas or pheochromocytomas. These terms can be used interchangeably but usually paraganglioma refer to a tumor originating from chromaffin cells outside the adrenal gland, which can also be called extra-adrenal pheochromocytoma, whereas pheochromocytoma typically refer to a tumor originating from the chromaffin cells within the adrenal gland.[2]

Chromaffin cells also settle near the vagus nerve and carotid arteries. In lower concentrations, extra-adrenal chromaffin cells also reside in the bladder wall, prostate, and behind the liver.

In non-mammals, chromaffin cells are found in a variety of places, generally not organised as an individual organ, and may be without innervation, relying only on endocrine or paracrine signals for secretion.[5][6]

Function
Adrenaline (Epinephrine)
Noradrenaline (Norepinephrine)

Chromaffin cells of the adrenal medulla are innervated by the splanchnic nerve and secrete adrenaline (epinephrine), noradrenaline (norepinephrine), some dopamine, enkephalin and enkephalin-containing peptides, and a few other hormones into the blood stream. The secreted adrenaline and noradrenaline play an important role in the sympathetic nervous system response, commonly called the fight-or-flight response. The enkephalins and enkephalin-containing peptides are related to, but distinct from endogenous peptides named endorphins (which are secreted from the pituitary); all of these peptides bind to opioid receptors and produce analgesic (and other) responses. The hormones are secreted from chromaffin granules; this is where the enzyme dopamine β-hydroxylase catalyses the conversion of dopamine to noradrenaline.[7] Distinct N and E cell forms exist (also Na and A cells in British nomenclature - noradrenaline and adrenaline); the former produce norepinephrine, the latter arise out of N cells through interaction with glucocorticoids, and convert norepinephrine into epinephrine.[8]

Catecholamine biosynthesis
Catecholamine biosynthesis

Clinical significance

Neoplasms arising from these cells are pheochromocytomas (also called chromaffin or sympathetic paragangliomas, in contrast to non-chromaffin or parasympathetic paragangliomas of glomus cells). Sometimes only neoplasms of adrenal origin are named pheochromocytomas, while others are named extra-adrenal paragangliomas.

Heart failure

Following heart failure, the body increases sympathetic activity to the adrenal medulla as the compensatory mechanism to increase heart rate and cardiac output. This increased sympathetic activity leads to chronically increased synthesis and secretion of catecholamines from the adrenal chromaffin cells. This chronic increase of epinephrine and norepinephrine secretion causes desensitization of the chromaffin cells to catecholamines resulting in a decrease in production and presence of α2 adrenergic receptors on their cell membrane. This desensitization and downregulation of α2 adrenergic receptors is caused by the upregulation of the enzyme Adrenal G protein coupled receptor kinase 2 (GRK2) which effectively eliminates the normal autocrine-type negative feedback that normally prevents the cells from over producing the catecholamines and replaces it with a positive feedback loop in which increased secretion further elicits more secretion.[9] This upregulation of GRK2 is also accompanied by upregulation and increased production of the enzyme tyrosine hydroxylase, which catalyzes the rate limiting step of catecholamine synthesis.[10]

History

The word "chromaffin" comes from a portmanteau of chromium and affinity. They are named as such because they can be visualised by staining with chromium salts. Chromium salts oxidise and polymerise catecholamines to form a brown color, most strongly in the cells secreting noradrenaline. Chromaffin cells are also called pheochromocytes.

The enterochromaffin cells are so named because of their histological similarity to chromaffin cells (they also stain yellow when treated with chromium salts), but their function is quite different and they are not derivatives of the neural crest.

Paraganglia are clusters of either chromaffin cells or glomus cells near sympathetic ganglia.

See also

References
  1. Schober, Andreas; Parlato, Rosanna; Huber, Katrin; Kinscherf, Ralf; Hartleben, Björn; Huber, Tobias B; Schütz, Günther; Unsicker, Klaus (2013). "Cell Loss and Autophagy in the Extra-Adrenal Chromaffin Organ of Zuckerkandl are Regulated by Glucocorticoid Signalling". Journal of Neuroendocrinology. 25 (1): 34–47. doi:10.1111/j.1365-2826.2012.02367.x. ISSN 0953-8194. PMC 3564403. PMID 23078542.
  2. "Chapter 179. The Paraganglionic System: The Paraganglia - Review of Medical Embryology Book - LifeMap Discovery". discovery.lifemapsc.com. Archived from the original on 2016-12-20. Retrieved 2017-06-03.
  3. "Chapter 164. The Autonomic Nervous System: The Sympathetic System - Review of Medical Embryology Book - LifeMap Discovery". discovery.lifemapsc.com. Archived from the original on 2017-05-05. Retrieved 2017-06-03.
  4. Schober, Andreas; Parlato, Rosanna; Huber, Katrin; Kinscherf, Ralf; Hartleben, Björn; Huber, Tobias B.; Schütz, Günther; Unsicker, Klaus (1 January 2013). "Cell Loss and Autophagy in the Extra-Adrenal Chromaffin Organ of Zuckerkandl are Regulated by Glucocorticoid Signalling". Journal of Neuroendocrinology. 25 (1): 34–47. doi:10.1111/j.1365-2826.2012.02367.x. PMC 3564403. PMID 23078542.
  5. Perry, SF; Capaldo, A (Nov 16, 2011). "The autonomic nervous system and chromaffin tissue: neuroendocrine regulation of catecholamine secretion in non-mammalian vertebrates". Autonomic Neuroscience: Basic and Clinical. 165 (1): 54–66. doi:10.1016/j.autneu.2010.04.006. PMID 20547474. S2CID 42402600.
  6. Pohorecky, LA; Wurtman, RJ (Mar 1971). "Adrenocortical control of epinephrine synthesis" (PDF). Pharmacological Reviews. 23 (1): 1–35. PMID 4941407. Archived from the original (PDF) on 2016-03-05. Retrieved 2013-03-01.
  7. Szewczyk, A; Lobanov, NA; Kicińska, A; Wójcik, G; Nałecz, MJ (2001). "ATP-sensitive K+ transport in adrenal chromaffin granules" (PDF). Acta Neurobiologiae Experimentalis. 61 (1): 1–12. PMID 11315316. Archived from the original (PDF) on 2017-08-09. Retrieved 2013-02-25.
  8. Young; Lowe; Stevens; Heath, eds. (2006). Wheater's Functional Histology (5th ed.). Edinburgh: Churchill Livingstone. ISBN 978-0-443-06850-8.
  9. Jafferjee, Malika; Reyes Valero, Thairy; Marrero, Christine; McCrink, Katie A.; Brill, Ava; Lymperopoulos, Anastasios (2016-03-01). "GRK2 Up-Regulation Creates a Positive Feedback Loop for Catecholamine Production in Chromaffin Cells". Molecular Endocrinology. 30 (3): 372–381. doi:10.1210/me.2015-1305. ISSN 0888-8809. PMC 5414648. PMID 26849467.
  10. Lymperopoulos, Anastasios; Rengo, Giuseppe; Gao, Erhe; Ebert, Steven N.; Dorn, Gerald W.; Koch, Walter J. (2010-05-21). "Reduction of Sympathetic Activity via Adrenal-targeted GRK2 Gene Deletion Attenuates Heart Failure Progression and Improves Cardiac Function after Myocardial Infarction". Journal of Biological Chemistry. 285 (21): 16378–16386. doi:10.1074/jbc.M109.077859. ISSN 0021-9258. PMC 2871505. PMID 20351116.

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