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Biology of the Heparanase-Heparan Sulfate Axis and Its Role in Disease Pathogenesis

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Publisher Thieme
Date 2021 Apr 1
PMID 33794549
Citations 17
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Abstract

Cell surface proteoglycans are important constituents of the glycocalyx and participate in cell-cell and cell-extracellular matrix (ECM) interactions, enzyme activation and inhibition, and multiple signaling routes, thereby regulating cell proliferation, survival, adhesion, migration, and differentiation. Heparanase, the sole mammalian heparan sulfate degrading endoglycosidase, acts as an "activator" of HS proteoglycans, thus regulating tissue hemostasis. Heparanase is a multifaceted enzyme that together with heparan sulfate, primarily syndecan-1, drives signal transduction, immune cell activation, exosome formation, autophagy, and gene transcription via enzymatic and nonenzymatic activities. An important feature is the ability of heparanase to stimulate syndecan-1 shedding, thereby impacting cell behavior both locally and distally from its cell of origin. Heparanase releases a myriad of HS-bound growth factors, cytokines, and chemokines that are sequestered by heparan sulfate in the glycocalyx and ECM. Collectively, the heparan sulfate-heparanase axis plays pivotal roles in creating a permissive environment for cell proliferation, differentiation, and function, often resulting in the pathogenesis of diseases such as cancer, inflammation, endotheliitis, kidney dysfunction, tissue fibrosis, and viral infection.

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References
1.
Gotte M . Syndecans in inflammation. FASEB J. 2003; 17(6):575-91. DOI: 10.1096/fj.02-0739rev. View

2.
Simizu S, Suzuki T, Muroi M, Lai N, Takagi S, Dohmae N . Involvement of disulfide bond formation in the activation of heparanase. Cancer Res. 2007; 67(16):7841-9. DOI: 10.1158/0008-5472.CAN-07-1053. View

3.
Gallagher J . Fell-Muir Lecture: Heparan sulphate and the art of cell regulation: a polymer chain conducts the protein orchestra. Int J Exp Pathol. 2015; 96(4):203-31. PMC: 4561558. DOI: 10.1111/iep.12135. View

4.
Sulka B, Lortat-Jacob H, Terreux R, Letourneur F, Rousselle P . Tyrosine dephosphorylation of the syndecan-1 PDZ binding domain regulates syntenin-1 recruitment. J Biol Chem. 2009; 284(16):10659-71. PMC: 2667753. DOI: 10.1074/jbc.M807643200. View

5.
Grootjans J, Zimmermann P, Reekmans G, Smets A, Degeest G, Durr J . Syntenin, a PDZ protein that binds syndecan cytoplasmic domains. Proc Natl Acad Sci U S A. 1998; 94(25):13683-8. PMC: 28366. DOI: 10.1073/pnas.94.25.13683. View