Sialyl-Lewis X

Sialyl-Lewis X
Identifiers
CAS number 98603-84-0 Y
PubChem 643990
ChemSpider 559072 Y
MeSH sialyl+Lewis+X
ChEMBL CHEMBL375586 Y
Jmol-3D images Image 1
Properties
Molecular formula C31H52N2O23
Molar mass 820.744 g/mol
 Y (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Sialyl LewisX, also known as sialyl LeX and SLeX, is a tetrasaccharide carbohydrate that is usually attached to O-glycans on the surface of cells. It is known to play a vital role in cell-to-cell recognition processes. It is also the means in which an egg attracts sperm - first to stick to it, then bond with it and eventually form a fetus. The discovery of the essential role that this tetrasaccharide plays in the fertilization process was reported in August 2011.[1]

Sialyl Lewis X is also one of the most important blood group antigens and is displayed on the terminus of glycolipids that are present on the cell surface. The Sialyl Lewis X determinant, E-selectin ligand carbohydrate structure, is constitutively expressed on granulocytes and monocytes and mediates inflammatory extravasation of these cells. Resting T and B lymphocytes lack its expression and are induced to strongly express sialyl Lewis X upon activation. The Sialyl Lewis X determinant is expressed preferentially on activated Th1 cells but not on Th2 cells.

Contents

History

The term Lewis in its name comes from the name of a family of people who suffered from a red blood cell incompatibility. The studies done on these individuals’ red blood cells led to the discovery of sialyl lewis x. Sialyl lewis x is a very important red blood cell antigen present on the glycolipids on the plasma membrane of the cell.

Clinical significance

Defective synthesis of the sialyl Lewis X antigen results in immunodeficiency (leukocyte adhesion deficiency type 2). Defective synthesis can be caused by the loss of fucosyltransferase, impairing the glycosylation of the glycosphingolipid.

Sialyl lewis x is being used in studies to fight tumors and cancer cell growth. It has been shown that there is frequent over expression of sialyl lewis x on cancer cells and is found on both N-glycan and O-glycans. Sialyl lewis x is being researched with CD markers to find new ways to create biosensors for cancer cells. Also, it is being used in new ways to target cancer cells specifically for cancer treatment.

It is also being used to achieve greater rates of fertilization of eggs in women by coating the eggs with sialyl lewis x. It plays a key role in the inflammatory response and may be used to increase the leukocyte response to infections.

Sialyl lewis x is an inflammation-associated antigen on liver cells. It becomes over expressed on diseased liver cells and can be used as a way to detect liver disease in a patient.

Sialyl lewis x is also being researched for detection and treatment of immune disorders because of its presence on leukocytes. There is congenital disorder where there is an inclination to recurring severe infections. This stems from an absence of sialyl lewis x attached to e-selectin on their neutrophils.

Function

Sialyl lewis x is important in leukocyte tethering and rolling. Leukocytes move through the blood stream and then tether themselves to the endothelial wall and roll along the endothelial tissue to determine if they want to leave the bloodstream to get to necessary tissue.

Sialyl lewis x is a necessary partner for the three selectins that bind the leukocyte and endothelial cells. When sialyl lewis x is part of an O-glycan and attached to CD34 it can then bind to L-selectin. For the binding to L-selectin to occur sialyl lewis x must undergo sulfation. For sialyl lewis x to attach to P-selectin it must bind to P-Selectin Glycoprotein Ligand-1 first which is then sulfated allowing sialyl lewis x to attach to P-selectin. For sialyl lewis x to bind to E-selectin it needs to be part of an N-glycan and then bind to CD44 or possibly glycolipids which have also been implicated to assist in binding. This binding allows the leukocytes to stick to and be released from the endothelial cells as needed to reach their destination.

Sialyl lewis x is also what allows the sperm cell to recognize the egg cell and form a fetus. It is a key part to the biochemical process of fertilization. Sialyl lewis x is also critical in the movement of cancer metastasis or the movement of cancer cells through the blood.

See also

References

  1. ^ Pang, Poh-Choo; Chiu, Lee, Chang, et al. (18). "Human Sperm Binding Is Mediated by the Sialyl-Lewisx Oligosaccharide on the Zona Pellucida". Science 333 (6050): 1761–1764. doi:10.1126/science.1207438. http://www.sciencemag.org/content/333/6050/1761.abstract. Retrieved 23 October 2011. 

Etzioni, Amos; Frydman, Moshe; Pollack, Shimon; Avidor, Israeli; Phillips, M. Laurie; Paulson, James C.; Gershoni-Baruch, Ruth; Recurrent Severe Infections Caused by a Novel Leukocyte Adhesion Deficiency. Journal Article (1992) New England Journal of Medicine 1789-1792; 327. http://www.nejm.org/doi/full/10.1056/NEJM199212173272505

Krishna K. Sarangapani, Jin Qian, Wei Chen, Veronika I. Zarnitsyna, Padmaja Mehta, Tadayuki Yago, Rodger P. McEver, and Cheng Zhu. Regulation of Catch Bonds by Rate of Force ApplicationJ. Biol. Chem. 2011 286: 32749-32761. First Published on July 20, 2011,doi:10.1074/jbc.M111.240044 Li-Hua Pan, Kohei Yamauchi, Takashi Sawai, Toshihide Nakadate, Yuki Kojima, Naofumi Takahashi, Keisuke Adachi, Akihiko Kameyama, and Hiroshi Inoue. Inhibition of Binding of E- and P-selectin to Sialyl-Lewis X Molecule Suppresses the Inflammatory Response in Hypersensitivity Pneumonitis in Mice Am. J. Respir. Crit. Care Med. 161: 1689-1697.

Human Sperm Binding Is Mediated by the Sialyl-Lewisx Oligosaccharide on the Zona Pellucida. Poh-Choo Pang, Philip C. N. Chiu, Cheuk-Lun Lee, Lan-Yi Chang, Maria Panico, Howard R. Morris,Stuart M. Haslam, Kay-Hooi Khoo, Gary F. Clark, William S. B. Yeung, and Anne Dell. Science 23 September 2011: 333 (6050), 1761-1764.Published online 18 August 2011[DOI:10.1126/science.1207438]

Sources