Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour. Issue 1 (26th December 2014)
- Record Type:
- Journal Article
- Title:
- Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour. Issue 1 (26th December 2014)
- Main Title:
- Syndecans: from peripheral coreceptors to mainstream regulators of cell behaviour
- Authors:
- Couchman, John R.
Gopal, Sandeep
Lim, Hooi Ching
Nørgaard, Steffen
Multhaupt, Hinke A.B. - Abstract:
- <abstract abstract-type="main" id="iep12112-abs-0001"> <title>Summary</title> <p>In the 25 years, as the first of the syndecan family was cloned, interest in these transmembrane proteoglycans has steadily increased. While four distinct members are present in mammals, one is present in invertebrates, including <italic>C. elegans</italic> that is such a powerful genetic model. The syndecans, therefore, have a long evolutionary history, indicative of important roles. However, these roles have been elusive. The knockout in the worm has a developmental neuronal phenotype, while knockouts of the syndecans in the mouse are mild and mostly limited to post‐natal rather than developmental effects. Moreover, their association with high‐affinity receptors, such as integrins, growth factor receptors, frizzled and slit/robo, have led to the notion that syndecans are coreceptors, with minor roles. Given that their heparan sulphate chains can gather many different protein ligands, this gave credence to views that the importance of syndecans lay with their ability to concentrate ligands and that only the extracellular polysaccharide was of significance. Syndecans are increasingly identified with roles in the pathogenesis of many diseases, including tumour progression, vascular disease, arthritis and inflammation. This has provided impetus to understanding syndecan roles in more detail. It emerges that while the cytoplasmic domains of syndecans are small, they have clear interactive<abstract abstract-type="main" id="iep12112-abs-0001"> <title>Summary</title> <p>In the 25 years, as the first of the syndecan family was cloned, interest in these transmembrane proteoglycans has steadily increased. While four distinct members are present in mammals, one is present in invertebrates, including <italic>C. elegans</italic> that is such a powerful genetic model. The syndecans, therefore, have a long evolutionary history, indicative of important roles. However, these roles have been elusive. The knockout in the worm has a developmental neuronal phenotype, while knockouts of the syndecans in the mouse are mild and mostly limited to post‐natal rather than developmental effects. Moreover, their association with high‐affinity receptors, such as integrins, growth factor receptors, frizzled and slit/robo, have led to the notion that syndecans are coreceptors, with minor roles. Given that their heparan sulphate chains can gather many different protein ligands, this gave credence to views that the importance of syndecans lay with their ability to concentrate ligands and that only the extracellular polysaccharide was of significance. Syndecans are increasingly identified with roles in the pathogenesis of many diseases, including tumour progression, vascular disease, arthritis and inflammation. This has provided impetus to understanding syndecan roles in more detail. It emerges that while the cytoplasmic domains of syndecans are small, they have clear interactive capabilities, most notably with the actin cytoskeleton. Moreover, through the binding and activation of signalling molecules, it is likely that syndecans are important receptors in their own right. Here, an overview of syndecan structure and function is provided, with some prospects for the future.</p> </abstract> … (more)
- Is Part Of:
- International journal of experimental pathology. Volume 96:Issue 1(2015:Feb.)
- Journal:
- International journal of experimental pathology
- Issue:
- Volume 96:Issue 1(2015:Feb.)
- Issue Display:
- Volume 96, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 96
- Issue:
- 1
- Issue Sort Value:
- 2015-0096-0001-0000
- Page Start:
- 1
- Page End:
- 10
- Publication Date:
- 2014-12-26
- Subjects:
- Pathology, Experimental -- Periodicals
616.07 - Journal URLs:
- http://www.blackwell-synergy.com/issuelist.asp?journal=iep ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2613 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/iep.12112 ↗
- Languages:
- English
- ISSNs:
- 0959-9673
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.244820
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4156.xml