User:Immcarle60/sandbox

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Note: Copied from Cell adhesion molecule

Cell adhesion molecules (CAMs) are proteins located on the cell surface[1] involved in binding with other cells or with the extracellular matrix (ECM) in the process called cell adhesion. In essence, cell adhesion molecules help cells stick to each other and to their surroundings. Cell adhesion molecules primarily help cells stick to each other and to their surroundings. Cell adhesion is a crucial component in maintaining tissue structure and function. In fully developed animals, these molecules play an integral role in creating force and movement and consequently ensure that organs are able to execute their functions. In addition to serving as "molecular glue", cell adhesion is important in affecting cellular mechanisms of growth, contact inhibition, and apoptosis. Often times aberrant expression of CAMs will result in diseases and conditions ranging from frostbite to cancer [2].

Structure[edit]

CAMs are typically transmembrane receptors and are composed of three conserved domains: an intracellular domain that interacts with the cytoskeleton, a transmembrane domain, and an extracellular domain. These proteins can interact in several different ways.[3] The first method is through homophilic binding, where CAMs bind with the same CAMs. They are also capable of heterophilic binding, meaning a CAM on one cell will bind with different CAMs on another cell. The final type of binding occurs between cells and substrate, where a mutual extracellular ligand that binds two different CAMs.

Families of CAMs[edit]

There are four major superfamilies or groups of CAMs: the immunoglobulin super family of cell adhesion molecules (IgCAMs), Cadherins, Integrins, and the Superfamily of C-type of lectin-like domains proteins (CTLDs). Proteoglycans are also considered to be a class of CAMs.

One classification system involves the distinction between calcium-independent CAMs and calcium-dependent CAMs.[4]Integrins and the Ig-superfamily CAMs do not depend on Ca2+ while cadherins and selectins depend on Ca2+. In addition, integrins participate in cell-matrix interactions, while other CAM families participate in cell-cell interactions.[5]

Calcium-independent[edit]

Integrins[edit]

Main article: Integrin

Integrins, one of the major classes of receptors within the ECM,[6] mediates cell-ECM interactions with collagen, fibrinogen, fibronectin, and vitronectin.[7] Integrins provide essential links between the extracellular environment and the intracellular signalling pathways, which can play roles in cell behaviours such as apoptosis, differentiation, survival, and transcription.[8]

Integrins are heterodimeric, as they consist of an alpha and beta subunit.[9] There are currently 18 alpha subunits and 8 beta subunits, which combine to make up 24 different integrin combinations.[7] Within each of the alpha and beta subunits there is a large extracellular domain, a transmembrane domain and a short cytoplasmic domain.[10] The extracellular domain is where the ligand binds through the use of divalent cations. In general, Mn2+
 increases affinity, Mg2+
 promotes adhesion to cells, and Ca2+
 decreases cell adhesion.[8] Integrins regulate their activity within the body by changing conformation. Most exist at rest in a low affinity state, which can be altered to high affinity through an external agonist which causes a conformational change within the integrin, increasing their affinity.[8]

An example of this is the aggregation of platelets;[8] Agonists such as thrombin or collagen trigger the integrin into its high affinity state, which causes increased fibrinogen binding, causing platelet aggregation.

IgSF CAMs[edit]

Main article: IgSF CAM

Immunoglobulin superfamily CAMs (IgSF CAMs) is regarded as the most diverse superfamily of CAMs. This family is characterized by their extracellular domains containing Ig-like domains. The Ig domains are then followed by Fibronectin type III domain repeats and IgSFs are anchored to the membrane by a GPI moiety. This family is involved in both homophilic or heterophilic binding and has the ability to bind integrins or different IgSF CAMs.

Calcium-dependent[edit]

Cadherins[edit]

Main article: Cadherin

The cadherins are homophilic Ca2+
-dependent glycoproteins.[11] The classic cadherins (E-, N- and P-) are concentrated at the intermediate cell junctions, which link to the actin filament network through specific linking proteins called catenins.[11]

Cadherins are notable in embryonic development. For example, it cadherins are crucial in gastrulation for the formation of the mesoderm, endoderm, and ectoderm. Each cadherin exhibits a unique pattern of tissue distribution that is carefully controlled by calcium. The diverse family of cadherins include epithelial (E-cadherins), placental (P-cadherins), neural (N-cadherins), retinal (R-cadherins), brain (B-cadherins and T-cadherins), and muscle (M-cadherins).[11] Many cell types express combinations of cadherin types.

The extracellular domain has major repeats called extracellular cadherin domains (ECD). Sequences involved in Ca2+
 binding between the ECDs are necessary for cell adhesion. The cytoplasmic domain has specific regions where catenin proteins bind.[12]

Selectins[edit]

Main article: Selectin

The selectins are a family of heterophilic CAMs that are dependent on fucosylated carbohydrates, e.g., mucins for binding. The three family members are E-selectin (endothelial), L-selectin (leukocyte), and P-selectin (platelet). The best-characterized ligand for the three selectins is P-selectin glycoprotein ligand-1 (PSGL-1), which is a mucin-type glycoprotein expressed on all white blood cells. Selectins have been implicated in several roles but they are especially important in the immune system by helping white blood cell homing and trafficking.[13]

Biological function of CAMs[edit]

The variety in CAMs leads to diverse functionality of these proteins in the biological setting. One of the CAMS that are particularly important in the lymphocyte homing are known as Addressins[14]. Lymphocyte homing is a key process occurring in a strong immune system. It controls the process of circulating lymphocytes adhering to particular regions and organs of the body[15]. The process is highly regulated by cell adhesion molecules, particularly, the addressin also known as MADCAM1. This antigen is known for its role in tissue-specific adhesion of lymphocytes to high endothelium venules[16]. Through these interactions they play a crucial role in orchestrating circulating lymphocytes.

CAM function in cancer metastasis, inflammation, and thrombosis makes it a viable therapeutic target that is currently being considered. For example, they block the metastatic cancer cells' ability to extravasate and home to secondary sites. This has been successfully demonstrated in in metastatic melanoma that hones to the lungs. In mice, when antibodies directed against CAMs in the lung endothelium were used as treatment there was a significant reduction in the number of metastatic sites [17].

See also[edit]

Wikimedia Commons has media related to Cell adhesion molecules.

References[edit]

  1. ^ Cell+Adhesion+Molecules at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ Korthuis, R. J.; Anderson, D. C.; Granger, D. N. (NaN). "Role of neutrophil-endothelial cell adhesion in inflammatory disorders". Journal of Critical Care. 9 (1): 47–71. ISSN 0883-9441. {{cite journal}}: Check date values in: |date= (help)
  3. ^ Chothia, Cyrus; Jones, E. Yvonne. "THE MOLECULAR STRUCTURE OF CELL ADHESION MOLECULES". Annual Review of Biochemistry. 66 (1): 823–862. doi:10.1146/annurev.biochem.66.1.823.
  4. ^ Brackenbury R, Rutishauser U, Edelman GM (January 1981). "Distinct calcium-independent and calcium-dependent adhesion systems of chicken embryo cells". Proc. Natl. Acad. Sci. U.S.A. 78 (1): 387–91. doi:10.1073/pnas.78.1.387. PMC 319058. PMID 6165990.
  5. ^ Lodish, Harvey; Berk, Arnold; Zipursky, S. Lawrence; Matsudaira, Paul; Baltimore, David; Darnell, James (2000-01-01). "Cell-Cell Adhesion and Communication". {{cite journal}}: Cite journal requires |journal= (help)
  6. ^ Brown, K; Yamada, K (1995), "The Role of Integrins during Vertebrae Development", Developmental Biology, 6: 69–77, doi:10.1016/s1044-5781(06)80016-2
  7. ^ a b Humphries JD, Byron A, Humphries MJ (October 2006). "Integrin ligands at a glance". J. Cell Sci. 119 (Pt 19): 3901–3. doi:10.1242/jcs.03098. PMC 3380273. PMID 16988024.
  8. ^ a b c d Schnapp, L (2006). Integrin, Adhesion/cell-matrix. Seattle: Elsevier.
  9. ^ García AJ (December 2005). "Get a grip: integrins in cell-biomaterial interactions". Biomaterials. 26 (36): 7525–9. doi:10.1016/j.biomaterials.2005.05.029. PMID 16002137.
  10. ^ Vinatier D (March 1995). "Integrins and reproduction". Eur J Obstet Gynecol Reprod Biol. 59 (1): 71–81. doi:10.1016/0028-2243(94)01987-I.
  11. ^ a b c Buxton RS, Magee AI (June 1992). "Structure and interactions of desmosomal and other cadherins". Semin. Cell Biol. 3 (3): 157–67. doi:10.1016/s1043-4682(10)80012-1. PMID 1623205.
  12. ^ Soncin, F.; Ward, M.C. (2011). "The Function of E-Cadherin in Stem Cell Pluripotency and Self-Renewal". Genes. 2 (1): 229–259. doi:10.3390/genes2010229.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  13. ^ Cavallaro, Ugo; Christofori, Gerhard (NaN). "Cell adhesion and signalling by cadherins and Ig-CAMs in cancer". Nature Reviews Cancer. 4 (2): 118–132. doi:10.1038/nrc1276. ISSN 1474-1768. {{cite journal}}: Check date values in: |date= (help)
  14. ^ Berg, Ellen Lakey; Goldstein, Leslie A.; Jimla, Mark A.; Nakache, Maurice; Picker, Louis J.; Streeter, Philip R.; Wu, Nora W.; Zhou, David; Butcher, Eugene C. (1 April 1989). "Homing Receptors and Vascular Addressins: Cell Adhesion Molecules that Direct Lymphocyte Traffic". Immunological Reviews. 108 (1): 5–18. doi:10.1111/j.1600-065X.1989.tb00010.x. ISSN 1600-065X.
  15. ^ Picker, Louis (1 June 1994). "Control of lymphocyte homing". Current Opinion in Immunology. 6 (3): 394–406. doi:10.1016/0952-7915(94)90118-X. ISSN 0952-7915.
  16. ^ Gorfu, Gezahegn; Rivera-Nieves, Jesús; Ley, Klaus (NaN). "Role of β7 integrins in intestinal lymphocyte homing and retention". Current molecular medicine. 9 (7): 836–850. ISSN 1566-5240. {{cite journal}}: Check date values in: |date= (help)
  17. ^ Andreoli, Thomas E.; Brown, A. M.; Fambrough, D. M.; Hoffman, Joseph F.; Schultz, Stanley G.; Welsh, Michael J. (2013). Molecular Biology of Membrane Transport Disorders. Springer Science & Business Media. ISBN 9781461311430.



Article evaluation

Is everything in the article relevant to the article topic? Is there anything that distracted you? The article isn't very robust and covers a few of the families of CAMs. Information that is currently provided seems appropriate and not biased towards any one view. Might be interesting to look at basic common functionality.

Check a few citations. Do the links work? Does the source support the claims in the article? Links work and they are primarily to peer-reviewed journal articles.

Is any information out of date? Is anything missing that could be added? Maybe we haven't gotten to this topic yet. What do you need to read to be able to understand this article? The talk page indicates that the most recent activity on this page occurred in 2013, so it hasn't been updated in a while. We have not talked in depth about CAMs so a recent literature search might help to figure out if there has been some interesting findings in the last 5 years.

Check out the Talk page of the article. What kinds of conversations, if any, are going on behind the scenes about how to represent this topic? 

Mainly just re-cateogrizing this page and a few content changes.

How is the article rated? Is it a part of any WikiProjects? 

It's part of the Biophysics and Molecular and cell Bio.

How does the way Wikipedia discusses this topic differ from the way we've talked about it in class? Maybe we haven't gotten to this topic yet. What do you need to read to be able to understand this article? Haven't gotten to CAMs yet so need to review literature/recent findings.


BIBLIOGRAPHY (Updated 1/27)

Albedlda, Steven M. and Buck, Clayton A. Integrins and other cell adhesion molecules. (1990) http://www.fasebj.org/doi/abs/10.1096/fasebj.4.11.2199285

Takeichi, Masatochi. Cadherins: A molecular family important in selective cell-cell adhesion. (1990) http://www.annualreviews.org/doi/pdf/10.1146/annurev.bi.59.070190.001321

Wong, Chee Wai, Dye, Danielle E., Coombe, Deidre. The Role of Immunoglobulin Superfamily Cell Adhesion Molecules in Cancer Metastasis. (2012) https://www.hindawi.com/journals/ijcb/2012/340296/

Roy, F. van, Berx, G. The cell-cell adhesion molecule E-cadherin. (2008) https://link.springer.com/article/10.1007/s00018-008-8281-1

Gallatin, Michael, St. John, Thomas P., Siegelman, Mark et al., Lymphocyte homing receptors.(2004) https://www.sciencedirect.com/science/article/pii/0092867486908329

Things to Do: (Updated 2/5)

  1. More inclusive Intro (waiting on a book chapter that I requested from the libe)
  2. I'd like to find citations for some of the quotations they make about lymphocyte homing molecules (Addressins) as well as the igSCF ICAM molecules/ I'm not really sure if Lymphocyte homing receptors need to be included... might think about taking out this line....
  3. Additionally, I'd like to use the first couple articles to talk about the functionality of the CAMs
  4. Maybe also creating a figure of the structure of these membrane associated receptors
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