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A desmosome (/ˈdɛzməˌsm/;[1][2] "binding body"), also known as a macula adhaerens (plural: maculae adhaerentes) (Latin for adhering spot), is a cell structure specialized for cell-to-cell adhesion. A type of junctional complex, they are localized spot-like adhesions randomly arranged on the lateral sides of plasma membranes. The desmosome was first discovered by Giulio Bizzozero, an Italian pathologist.[3] He named these “dense nodules” the “nodes of Bizzozero." In 1920, the term “desmosome” was termed by Josef Schaffer. The first combining form, desmo-, New Latin from Greek desmos, bond, carries meaning of binding or bonding things together. Combined with -some, which comes from soma, body, it thus makes a desmosome a "binding body."

Desmosome
Desmosome cell junction en.svg
A desmosome.
Desmosome - 2.png
The extracellular core region containing desmocollin and desmoglein, and the plaque contain desmoplakin, which attaches to keratin intermediate filaments.
Details
Identifiers
Latin Desmosoma
Macula adhaerens
TH H1.00.01.1.02015
FMA 67412
Anatomical terminology

Desmosomes are one of the stronger cell-to-cell adhesion types and are found in tissue that experience intense mechanical stress, such as cardiac muscle tissue, bladder tissue, gastrointestinal mucosa, and epithelia.[3]

Contents

StructureEdit

Desmosomes are composed of desmosome-intermediate filament complexes (DIFC), which is a network of cadherin proteins, linker proteins and keratin intermediate filaments.[4] The DIFCs can be broken into three regions: the extracellular core region, or desmoglea, the outer dense plaque, or ODP, and the inner dense plaque, or IDP.[3]

The extracellular core region, approximately 34 nm in length, contains desmoglein and desmocollin, which are in the cadherin family of cell adhesion proteins. Both have five extracellular domains, and have calcium-binding motifs.  Extracellular calcium helps form the cadherin adhesion by allowing the cadherin extracellular domain on desmoglein and desmocollin to become rigid.[5] They bind to each other via homophilic interactions in the extracellular space near their N-termini. Desmoglein and desmocollin have a single pass transmembrane region plus an intracellular anchor to secure its position in the cell membrane. Desmogleins and the desmocollin Dsc “a” form contain an intracellular cadherin domain, which binds to plakoglobin.[3]

The outer dense plaque, which is about 15-20 nm in length, contains the intracellular ends of desmocollin and desmoglein, the N-terminus side of desmoplakin, and the armadillo family of mediatory proteins plakoglobin and plakophilin.[3] Armadillo proteins are involved in mediating attachment to intracellular filaments and cell membrane proteins. Armadillo proteins consist of β-catenin, p120-catenin, plakoglobin (γ-catenin), and plakophilins 1-3. In desmosomes, plakoglobin and plakophilin help secure desmoplakin and keratin filaments to the desmosome structure. Plakoglobin has 12-arm repeats with a head and tail structure. Plakophillins have 9-arm repeats, and exist in 2 isoforms: a shorter “a” form and longer “b” form.

The inner dense plaque, also about 15-20 nm in length, contains the C-terminus end of desmoplakin and their attachment to keratin intermediate filaments. Desmoplakin is the most abundant part of the desmosome,[6] as is operates as the mediator between the cadherin proteins in the plasma membrane and the keratin filaments. Desmoplakin has two isoforms that differ in the length of their middle rod domain. All desmoplakins have an N-terminal head, a C-tail consisting of three plakin repeats, and a glycine-serine-arginine rich domain (GSR) at the C-end.

DiseasesEdit

Mutations within the desmosome are the main cause of Arrhythmogenic right ventricular cardiomyopathy (ARVC),a life-threatening disease caused by mutations usually in Desmoglein 2, but sometimes in Desmocollin 2. It often afflicts (although not exclusive to) young male athletes. The current incidence within the population is accepted as 1/10,000 however it is thought that 1/200 may have a mutation that may predispose to ARVC.[7] Symptoms of ARVC include fainting, shortness of breath, and heart palpitations and the condition is treated by implanting a small defibrillator device.

Blistering diseases such as Pemphigus vulgaris (PV) and Pemphigus foliaceus (PF) are autoimmune diseases in which auto-antibodies target demsogleins. PV is caused by circulating autoantibodies (IgG) that target Dsg3 (Desmoglein 3) and sometimes Dsg1. PV is manifested by suprabasal acantholysis, or blisters in the mucus membrane and blisters in the epidermis. PF patients have autoantibodies that target Dsg1 with superficial blisters on the epidermis with no mucus membrane issues. Both disease result in a loss of keratinocyte adhesion. Pemphigus can also be caused by a bacterial infection: bullous impetigo is an infection caused by a staphylococcus bacterium that releases a toxin that cleaves the Dsg1 extracellular domain.

Similar symptoms occur with Hailey–Hailey disease, though the cause is not autoimmune but genetic. A haploinsufficiency of the ATP2C1 gene located on chromosome 3, which encodes the protein hSPCA1, causes malformation of the desmosomes.

Desmoglein 1 haploinsufficiency leads to striate palmoplantar keratoderma, a disease which causes extreme thickening of the epidermis. Loss of Desmoglein 4 leads to defective hair-follicle differentiation.[3]

Epidermolysis bullosa simplex is an epidermal blistering disease caused by mutations in genes coding for keratin 5 and 14, which attach to desmoplakin. This disease manifests as rupture of the basal epidermis when stress is applied. Mild instances of this condition tend to affect the hands and feet while more severe cases can cause blistering over the entire body.[8] Ectodermal dysplasia or skin fragility syndrome is caused by Plakophillin 1 mutations. This is manifested by detachment of intermediate filaments and desmoplakin from the desmosome.[4]

See alsoEdit

ReferencesEdit

  1. ^ "Desmosome". Oxford Dictionaries. Oxford University Press. Retrieved 2016-01-21. 
  2. ^ "Desmosome". Merriam-Webster Dictionary. Retrieved 2016-01-21. 
  3. ^ a b c d e f Delva, Emmanuella; Tucker, Dana K.; Kowalczyk, Andrew P. (August 2009). "The desmosome". Cold Spring Harbor Perspectives in Biology. 1 (2): a002543. doi:10.1101/cshperspect.a002543. ISSN 1943-0264. PMC 2742091 . PMID 20066089. 
  4. ^ a b Garrod, David; Chidgey, Martyn (2008-03-01). "Desmosome structure, composition and function". Biochimica et Biophysica Acta (BBA) - Biomembranes. Apical Junctional Complexes Part I. 1778 (3): 572–587. doi:10.1016/j.bbamem.2007.07.014. 
  5. ^ Pokutta, Sabine; Weis, William I. (2007). "Structure and mechanism of cadherins and catenins in cell-cell contacts". Annual Review of Cell and Developmental Biology. 23: 237–261. doi:10.1146/annurev.cellbio.22.010305.104241. ISSN 1081-0706. PMID 17539752. 
  6. ^ Mueller, H.; Franke, W. W. (1983-02-05). "Biochemical and immunological characterization of desmoplakins I and II, the major polypeptides of the desmosomal plaque". Journal of Molecular Biology. 163 (4): 647–671. ISSN 0022-2836. PMID 6341602. 
  7. ^ Lahtinen, AM; Lehtonen, E; Marjamaa, A; Kaartinen, M; Heliö, T; Porthan, K; Oikarinen, L; Toivonen, L; Swan, H; Jula, A; Peltonen, L; Palotie, A; Salomaa, V; Kontula, K (2011). "Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy". Heart Rhythm. 8 (8): 1214–21. doi:10.1016/j.hrthm.2011.03.015. PMID 21397041. 
  8. ^ "Desmosomes". biologydictionary.net. Retrieved 27 December 2017. 

External linksEdit