Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2002 May-Jun;19(4-5):295-304.
doi: 10.1023/A:1025352501148.

Unlocking the secrets of syndecans: transgenic organisms as a potential key

Affiliations
Review

Unlocking the secrets of syndecans: transgenic organisms as a potential key

Robert Bellin et al. Glycoconj J. 2002 May-Jun.

Abstract

Heparan sulfate proteoglycans are known to modulate the activity of a large number of extracellular ligands thereby having the potential to regulate a great diversity of biological processes. The long-term studies in our laboratory have focused on the syndecans, one of the major cell surface heparan sulfate proteoglycan families. Most early work on syndecans involved biochemical studies that provided initial information on their structure and putative biological roles. In recent years, the development of transgenic organisms has allowed a more complete understanding of syndecan function. Studies with transgenic syndecan-1 and syndecan-3 mice have demonstrated an unforeseen role for syndecans in the regulation of feeding behavior. Syndecan-1 knockout mice display a reduced susceptibility to both Wnt-induced tumorigenesis and microbial pathogenesis. Experiments with Drosophila show that syndecan is first expressed upon cellularization in the early embryo, and may play a role in the early developmental stages of the fly. This review focuses on these diverse functions of the syndecans that have been elucidated by the use of transgenic mice and Drosophila as model systems.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Int J Dev Biol. 2002 May;46(3):267-78 - PubMed
    1. Nature. 1999 Jul 15;400(6741):281-4 - PubMed
    1. Nature. 2001 May 17;411(6835):349-54 - PubMed
    1. Nat Genet. 2000 Jul;25(3):329-32 - PubMed
    1. Cell. 1997 Nov 28;91(5):605-15 - PubMed

MeSH terms

LinkOut - more resources