Mast cell

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Mast cell
SMCpolyhydroxysmall.jpg
Mast cells
Latinmastocytus
CodeTH H2.00.03.0.01010
 
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Mast cell
SMCpolyhydroxysmall.jpg
Mast cells
Latinmastocytus
CodeTH H2.00.03.0.01010

A mast cell (also known as mastocyte and labrocyte[1]) is a resident cell of several types of tissues and contains many granules rich in histamine and heparin. Although best known for their role in allergy and anaphylaxis, mast cells play an important protective role as well, being intimately involved in wound healing and defense against pathogens.[2]

The mast cell is very similar in both appearance and function to the basophil, a type of white blood cell. However, they are not the same, as they arise from different cell lines.[3]

Origin and classification[edit]

Illustration depicting mast cell activation and anaphylaxis
Mast cell

Mast cells were first described by Paul Ehrlich in his 1878 doctoral thesis on the basis of their unique staining characteristics and large granules. These granules also led him to the incorrect belief that they existed to nourish the surrounding tissue, so he named them "Mastzellen" (from the German: Mast, "fattening" as of animals).[4][5] They are now considered to be part of the immune system.

Mast cells are very similar to basophil granulocytes (a class of white blood cells) in blood. Both are granulated cells that contain histamine and heparin, an anticoagulant. Both cells also release histamine upon binding to immunoglobulin E.[3] These similarities have led many to speculate that mast cells are basophils that have "homed in" on tissues. Furthermore they share a common precursor in bone marrow expressing the CD34 molecule. Basophils leave the bone marrow already mature, whereas the mast cell circulates in an immature form, only maturing once in a tissue site. The site an immature mast cell settles in probably determines its precise characteristics.[2] The first in vitro differentiation and growth of a pure population of mouse mast cells has been carried out using conditioned medium derived from concanavalin A-stimulated splenocytes.[6] Later, it was discovered that T cell-derived interleukin 3 was the component present in the conditioned media that was required for mast cell differentiation and growth.[7]

Two types of mast cells are recognized, those from connective tissue and a distinct set of mucosal mast cells. The activities of the latter are dependent on T-cells.[8]

Mast cells are present in most tissues characteristically surrounding blood vessels and nerves, and are especially prominent near the boundaries between the outside world and the internal milieu, such as the skin, mucosa of the lungs and digestive tract, as well as in the mouth, conjunctiva and nose.[2]

Physiology[edit]

The role of mast cells in the development of allergy.

Mast cells play a key role in the inflammatory process. When activated, a mast cell rapidly releases its characteristic granules and various hormonal mediators into the interstitium. Mast cells can be stimulated to degranulate by direct injury (e.g. physical or chemical [such as opioids, alcohols, and certain antibiotics such as polymyxins]), cross-linking of Immunoglobulin E (IgE) receptors, or by activated complement proteins.[2]

Mast cells express a high-affinity receptor (FcεRI) for the Fc region of IgE, the least-abundant member of the antibodies. This receptor is of such high affinity that binding of IgE molecules is essentially irreversible. As a result, mast cells are coated with IgE, which is produced by plasma cells (the antibody-producing cells of the immune system). IgE molecules, like all antibodies, are specific to one particular antigen.

In allergic reactions, mast cells remain inactive until an allergen binds to IgE already in association with the cell (see above). Other membrane activation events can either prime mast cells for subsequent degranulation or can act in synergy with FcεRI signal transduction.[9] Allergens are generally proteins or polysaccharides. The allergen binds to the antigen-binding sites, which are situated on the variable regions of the IgE molecules bound to the mast cell surface. It appears that binding of two or more IgE molecules (cross-linking) is required to activate the mast cell. The clustering of the intracellular domains of the cell-bound Fc receptors, which are associated with the cross-linked IgE molecules, causes a complex sequence of reactions inside the mast cell that lead to its activation. Although this reaction is most well understood in terms of allergy, it appears to have evolved as a defense system against intestinal worm infestations (tapeworms, etc.)[citation needed].

The molecules thus released into the extracellular environment include:[2]

Structure of histamine

Histamine dilates post-capillary venules, activates the endothelium, and increases blood vessel permeability. This leads to local edema (swelling), warmth, redness, and the attraction of other inflammatory cells to the site of release. It also depolarizes nerve endings (leading to itching or pain). Cutaneous signs of histamine release are the "flare and wheal"-reaction. The bump and redness immediately following a mosquito bite are a good example of this reaction, which occurs seconds after challenge of the mast cell by an allergen.[2]

The other physiologic activities of mast cells are much less well-understood. Several lines of evidence suggest that mast cells may have a fairly fundamental role in innate immunity – they are capable of elaborating a vast array of important cytokines and other inflammatory mediators such as TNFa, they express multiple "pattern recognition receptors" thought to be involved in recognizing broad classes of pathogens, and mice without mast cells seem to be much more susceptible to a variety of infections.[citation needed]

Mast cell granules carry a variety of bioactive chemicals. These granules have been found to be transferred to adjacent cells of the immune system and neurons in a process of transgranulation via mast cell pseudopodia.[10]

Role in disease[edit]

Allergic disease[edit]

Many forms of cutaneous and mucosal allergy are mediated in large part by mast cells; they play a central role in asthma, eczema, itch (from various causes) and allergic rhinitis and allergic conjunctivitis. Antihistamine drugs act by blocking histamine action on nerve endings. Cromoglicate-based drugs (sodium cromoglicate, nedocromil) block a calcium channel essential for mast cell degranulation, stabilizing the cell and preventing release of histamine and related mediators. Leukotriene antagonists (such as montelukast and zafirlukast) block the action of leukotriene mediators and are being used increasingly in allergic diseases.[2]

Calcium triggers the secretion of histamine from mast cells after previous exposure to sodium fluoride. The secretory process can be divided into a fluoride-activation step and a calcium-induced secretory step. It was observed that the fluoride-activation step is accompanied by an elevation of cAMP levels within the cells. The attained high levels of cAMP persist during histamine release. It was further found that catecholamines do not markedly alter the fluoride-induced histamine release. It was also confirmed that the second, but not the first, step in sodium fluoride-induced histamine secretion is inhibited by theophylline.[11] Vasodilation and increased permeability of capillaries are a result of both H1 and H2 receptor types.[12]

Stimulation of histamine activates a histamine (H2)-sensitive adenylate cyclase of oxyntic cells, and there is a rapid increase in cellular [cAMP] that is involved in activation of H+ transport and other associated changes of oxyntic cells.[13]

Anaphylaxis[edit]

In anaphylaxis (a severe systemic reaction to allergens, such as nuts, bee stings, or drugs), body-wide degranulation of mast cells leads to vasodilation and, if severe, symptoms of life-threatening shock.[citation needed]

Histamine is a vasodilatory substance released during anaphylaxis.[14]

Autoimmunity[edit]

Mast cells are implicated in the pathology associated with the autoimmune disorders rheumatoid arthritis, bullous pemphigoid, and multiple sclerosis. They have been shown to be involved in the recruitment of inflammatory cells to the joints (e.g., rheumatoid arthritis) and skin (e.g. bullous pemphigoid) and this activity is dependent on antibodies and complement components.[15]

Reproductive disorders[edit]

Mast cells are present within the endometrium, with increased activation and release of mediators in endometriosis.[16] In males, mast cells are present in the testes and are increased in oligo- and azoospermia, with mast cell mediators directly suppressing sperm motility in a potentially reversible manner.[16]

Mast cell disorders[edit]

Mastocytosis is a rare condition featuring proliferation of mast cells. It exists in a cutaneous and systemic form, with the former being limited to the skin and the latter involving multiple organs.[2] Mast cell tumors are often seen in dogs and cats.[17]

Histological staining[edit]

Toluidine blue: one of the most common stains for acid mucopolysaccharides and glycoaminoglycans, components of mast cells granules.[18]

Surface markers: Cell surface markers of mast cells were referred in detail by Heneberg,[19] claiming that mast cells may be inadverently included in the stem or progenitor cell isolates since part of them is positive for the CD34 antigen. The classical mast cell markers include the high affinity IgE receptor, CD25 (non-neoplastic mast cells), CD117 (c-Kit), CD23, and CD203c (for most of the mast cell populations). Expression of some molecules may change in course of the mast cell activation.[20]

References[edit]

  1. ^ "labrocytes". Memidex. 
  2. ^ a b c d e f g h Prussin C, Metcalfe DD (2003). "IgE, mast cells, basophils, and eosinophils". J Allergy Clin Immunol 111 (2 Suppl): S486–94. doi:10.1067/mai.2003.120. PMID 12592295. 
  3. ^ a b Marieb, Elaine N. & Katja Hoehn. Human Anatomy and Physiology. Seventh edition. San Francisco: Pearson Benjamin Cummings, 2007. pg. 659.
  4. ^ Ehrlich P. Beiträge zur Theorie und Praxis der histologischen Färbung. Dissertation at Leipzig University, 1878.
  5. ^ [1]
  6. ^ Razin E, Cordon-Cardo C, Good RA (April 1981). "Growth of a pure population of mouse mast cells in vitro with conditioned medium derived from concanavalin A-stimulated splenocytes.". Proc Natl Acad Sci U S A. 78 (4): 2559–61. PMC 319388. PMID 6166010. 
  7. ^ Razin E, Ihle JN, Seldin D, Mencia-Huerta JM, Katz HR, LeBlanc PA, Hein A, Caulfield JP, Austen KF, Stevens RL. (March 1984). "Interleukin 3: A differentiation and growth factor for the mouse mast cell that contains chondroitin sulfate E proteoglycan.". J Immunol. 132 (3): 1479–86. PMID 6198393. 
  8. ^ Denburg, Judah A. (1998). Allergy and allergic diseases: the new mechanisms and therapeutics. Totowa, NJ: Humana Press. ISBN 0-89603-404-6. 
  9. ^ Pulendran B, Ono SJ (May 2008). "A shot in the arm for mast cells". Nat. Med. 14 (5): 489–90. doi:10.1038/nm0508-489. PMID 18463655. 
  10. ^ Wilhelm M, Silver R, Silverman AJ (November 2005). "Central nervous system neurons acquire mast cell products via transgranulation". Eur. J. Neurosci. 22 (9): 2238–48. doi:10.1111/j.1460-9568.2005.04429.x. PMID 16262662. 
  11. ^ Agents and Actions, 1983, Volume 13, Issue 2-3, pp 132-137 Sodium fluoride evoked histamine release from mast cells. A study of cyclic AMP levels and effects of catecholamines Per E. Alm
  12. ^ Dachman WD, et al. Journal J Allergy Clin Immunol. 1994 Mar;93(3):606-14
  13. ^ Am J Physiol. 1982 Feb;242(2):G79-84.
  14. ^ Dachman WD, et al. J Allergy Clin Immunol. 1994 Mar;93(3):606-14
  15. ^ David M. Lee, Daniel S. Friend, Michael F. Gurish, Christophe Benoist, Diane Mathis, Michael B. Brenner. (2002.) "Mast Cells: A Cellular Link Between Autoantibodies and Inflammatory Arthritis", Science, 297(5587):1689-92.
  16. ^ a b Menzies, F. M.; Shepherd, M. C.; Nibbs, R. J.; Nelson, S. M. (2010). "The role of mast cells and their mediators in reproduction, pregnancy and labour". Human Reproduction Update 17 (3): 383–396. doi:10.1093/humupd/dmq053. PMID 20959350.  edit
  17. ^ "Cutaneous Mast Cell Tumors". The Merck Veterinary Manual. 2006. Retrieved 2007-07-08. 
  18. ^ Nelly Blumenkrantz and Gustav Asboe-Hansen. (1975.) "A selective stain for mast cells", The Histochemical Journal, 7(3):277-82.
  19. ^ Heneberg, Petr (2011). "Mast cells and basophils: trojan horses of conventional lin- stem/progenitor cell isolates". Current Pharmaceutical Design 17 (34): 3753–3771. PMID 22103846. Retrieved 21 May 2012. 
  20. ^ Lebduska, Pavel; Korb J, Tumova M, Heneberg P, Draber P (2007). "Topography of signaling molecules as detected by electron microscopy on plasma membrane sheets isolated from non-adherent mast cells". Journal of Immunological Methods 328 (1-2): 139–151. doi:10.1016/j.jim.2007.08.015. PMID 17900607. Retrieved 21 May 2012. 

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