Cytokeratin
Cytokeratins are keratin proteins found in the intracytoplasmic cytoskeleton of epithelial tissue. They are an important component of intermediate filaments, which help cells resist mechanical stress.[1] Expression of these cytokeratins within epithelial cells is largely specific to particular organs or tissues. Thus they are used clinically to identify the cell of origin of various human tumors.
Naming
The term "cytokeratin" began to be used in the late 1970s, when the protein subunits of keratin intermediate filaments inside cells were first being identified and characterized.[2] In 2006 a new systematic nomenclature for mammalian keratins was created, and the proteins previously called "cytokeratins" are simply called keratins (human epithelial category). For example, cytokeratin-4 (CK-4) has been renamed keratin-4 (K4).[3] However, they are still commonly referred to as cytokeratins in clinical practice.
Types
There are two categories of cytokeratins: the acidic type I cytokeratins and the basic or neutral type II cytokeratins. Within each category, cytokeratins are numbered in order of decreasing size, from low molecular weight (LMWCKs) to high molecular weight (HMWCKs). Cytokeratins are usually found in heterodimeric pairs of acidic and basic subunits of similar size.[4]
| Basic CK (Type B / Class II) | Acidic CK (Type A / Class I) | |
|---|---|---|
| HMWCK "squamous keratins" |
CK-1 CK-2 CK-3 CK-4 CK-5 CK-6 | CK-9 CK-10 CK-11 CK-12 CK-13 CK-14 CK-15 CK-16 CK-17 |
| LMWCK "simple keratins" |
CK-7 CK-8 | CK-18 CK-19 CK-20 |
Expression of these cytokeratins is largely organ or tissue specific. The subsets of cytokeratins which an epithelial cell expresses depends mainly on the type of epithelium, the moment in the course of terminal differentiation and the stage of development. Thus a specific cytokeratin expression profile allows the identification of epithelial cells. Furthermore, this applies also to the malignant counterparts of the epithelia, (carcinomas), as the cytokeratin profile is generally retained. Thus the study of cytokeratin expression by immunohistochemistry techniques is a tool of immense value widely used for tumor diagnosis and characterization in surgical pathology.[5]
| Cytokeratin | Sites |
|---|---|
| Cytokeratin 4 |
|
| Cytokeratin 7 |
|
| Cytokeratin 8 |
|
| Cytokeratin 10 |
|
| Cytokeratin 13 |
|
| Cytokeratin 14 |
|
| Cytokeratin 18 |
|
| Cytokeratin 19 |
Does not react with hepatocytes and hepatocellular carcinoma[6] |
| Cytokeratin 20 |
|
Molecular biology
The cytokeratins are encoded by a family encompassing 30 genes. Among them, 20 are epithelial genes and the remaining 10 are specific for trichocytes.
All cytokeratin chains are composed of a central α-helix-rich domain (with a 50-90% sequence identity among cytokeratins of the same type and around 30% between cytokeratins of different type) with non-α-helical N- and C-terminal domains. The α-helical domain has 310-150 amino acids and comprises four segments in which a seven-residue pattern repeats. Into this repeated pattern, the first and fourth residues are hydrophobic and the charged residues show alternate positive and negative polarity, resulting in the polar residues being located on one side of the helix. This central domain of the chain provides the molecular alignment in the keratin structure and makes the chains form coiled dimers in solution.
The end-domain sequences of type I and II cytokeratin chains contain in both sides of the rod domain the subdomains V1 and V2, which have variable size and sequence. The type II also presents the conserved subdomains H1 and H2, encompassing 36 and 20 residues respectively. The subdomains V1 and V2 contain residues enriched by glycines and/or serines, the former providing the cytokeratin chain a strong insoluble character and facilitating the interaction with other molecules. These terminal domains are also important in the defining the function of the cytokeratin chain characteristic of a particular epithelial cell type.
Two dimers of cytokeratin groups into a keratin tetramer by anti-parallel binding. This cytokeratin tetramer is considered to be the main building block of the cytokeratin chain. By head-to-tail linking of the cytokeratin tetramers, the protofilaments are originated, which in turn intertwine in pairs to form protofibrils. Four protofibrils give place to one cytokeratin filament.
Cell biology
In the cytoplasm, the keratin filaments conform a complex network which extends from the surface of the nucleus to the cell membrane. Numerous accessory proteins are involved in the genesis and maintenance of such structure.
This association between the plasma membrane and the nuclear surface provides important implications for the organization of the cytoplasm and cellular communication mechanisms. Apart from the relatively static functions provided in terms of supporting the nucleus and providing tensile strength to the cell, the cytokeratin networks undergo rapid phosphate exchanges mediated depolymerization, with important implications in the more dynamic cellular processes such as mitosis and post-mitotic period, cell movement and differentiation.
Cytokeratins interact with desmosomes and hemidesmosomes, thus collaborating to cell-cell adhesion and basal cell-underlying connective tissue connection.
The intermediate filaments of the eukaryotic cytoskeleton, which the cytokeratins are one of its three components, have been probed to associate also with the ankyrin and spectrin complex protein network that underlies the cell membrane.
References
- ↑ Herrmann H, Bär H, Kreplak L, Strelkov SV, Aebi U (July 2007). "Intermediate filaments: from cell architecture to nanomechanics". Nat. Rev. Mol. Cell Biol. 8 (7): 562–73. PMID 17551517. doi:10.1038/nrm2197.
- ↑ Franke WW, Schmid E, Osborn M, Weber K (June 1979). "Intermediate-sized filaments of human endothelial cells". The Journal of Cell Biology. 81 (3): 570–80. PMC 2110384
. PMID 379021. doi:10.1083/jcb.81.3.570. - ↑ Schweizer J, Bowden PE, Coulombe PA, et al. (July 2006). "New consensus nomenclature for mammalian keratins". The Journal of Cell Biology. 174 (2): 169–74. PMC 2064177 . PMID 16831889. doi:10.1083/jcb.200603161.
- ↑ Rekhtman, Natasha; Bishop, Justin A. (2011). Quick Reference Handbook for Surgical Pathologists. Heidelberg: Springer. pp. 4–8. ISBN 978-3-642-20085-4.
- ↑ Dabbs, DJ (2010). Diagnostic Immunohistochemistry: Theranostic and Genomic Applications (3rd ed.). New York: Saunders.
- 1 2 3 4 5 6 7 8 9 10 11 12 13 MUbio > MONOCLONAL ANTIBODIES TO CYTOKERATINS Retrieved October 2010
External links
- Cytokeratin at the US National Library of Medicine Medical Subject Headings (MeSH)