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PMID: 15503855 Published · ppublish English Journal Article Review

Hyaluronan catabolism: a new metabolic pathway.

European journal of cell biology ·Vol. 83 ·No. 7 ·2004-08-00 ·Pages 317-25

Stern R

Abstract

A new pathway of intermediary metabolism is described involving the catabolism of hyaluronan. The cell surface hyaluronan receptor, CD44, two hyaluronidases, Hyal-1 and Hyal-2, and two lysosomal enzymes, beta-glucuronidase and beta-N-acetylglucosaminidase, are involved. This metabolic cascade begins in lipid raft invaginations at the cell membrane surface. Degradation of the high-molecular-weight extracellular hyaluronan occurs in a series of discreet steps generating hyaluronan chains of decreasing sizes. The biological functions of the oligomers at each quantum step differ widely, from the space-filling, hydrating, anti-angiogenic, immunosuppressive 10(4)-kDa extracellular polymer, to 20-kDa intermediate polymers that are highly angiogenic, immuno-stimulatory, and inflammatory. This is followed by degradation to small oligomers that can induce heat shock proteins and that are anti-apoptotic. The single sugar products, glucuronic acid and a glucosamine derivative are released from lysosomes to the cytoplasm, where they become available for other metabolic cycles. There are 15 g of hyaluronan in the 70-kg individual, of which 5 g are cycled daily through this pathway. Some of the steps in this catabolic cascade can be commandeered by cancer cells in the process of growth, invasion, and metastatic spread.

MeSH Terms
Animals Apoptosis/immunology,physiology Glucosamine/immunology,metabolism Glucuronic Acid/immunology,metabolism Glycoside Hydrolases/immunology,metabolism Humans Hyaluronan Receptors/immunology,metabolism Hyaluronic Acid/immunology,metabolism Lysosomes/metabolism Membrane Microdomains/immunology,metabolism Mice Mucolipidoses/metabolism Neoplasms/immunology,metabolism Neovascularization, Physiologic/immunology,physiology
Chemicals
Hyaluronan Receptors Glucuronic Acid Hyaluronic Acid Glycoside Hydrolases Glucosamine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Stern Robert
Department of Pathology, School of Medicine, University of California, San Francisco, 513 Parnassus Avenue, S-564, San Francisco, CA 94143-0511, USA. [email protected]
Article Info
Journal
European journal of cell biology
Abbr.
Eur J Cell Biol
ISSN
0171-9335
Published
2004-08-00
Pages
317-25
Language
English
Region
Germany
NLM ID
7906240
Subset
IM
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