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Glycobiology and Extracellular Matrices
2 Results
- Glycobiology and Extracellular MatricesOpen Access
Tumor Necrosis Factor-stimulated Gene-6 (TSG-6) Is Constitutively Expressed in Adult Central Nervous System (CNS) and Associated with Astrocyte-mediated Glial Scar Formation following Spinal Cord Injury
Journal of Biological ChemistryVol. 291Issue 38p19939–19952Published online: July 19, 2016- Vivien J. Coulson-Thomas
- Mark E. Lauer
- Sara Soleman
- Chao Zhao
- Vincent C. Hascall
- Anthony J. Day
- and others
Cited in Scopus: 45Tumor necrosis factor (TNF)-stimulated gene-6 (TSG-6) binds to hyaluronan and can reorganize/stabilize its structure, also enhancing the binding of this glycosaminoglycan to its cell surface receptor, CD44. TSG-6 is rapidly up-regulated in response to inflammatory cytokines protecting tissues from the damaging effects of inflammation. Despite TSG-6 treatment having been shown to improve outcomes in an experimental model of traumatic brain injury, TSG-6 expression has not been extensively studied in the central nervous system (CNS). - Glycobiology and Extracellular MatricesOpen Access
The Anti-inflammatory Protein TSG-6 Regulates Chemokine Function by Inhibiting Chemokine/Glycosaminoglycan Interactions
Journal of Biological ChemistryVol. 291Issue 24p12627–12640Published online: April 4, 2016- Douglas P. Dyer
- Catherina L. Salanga
- Scott C. Johns
- Elena Valdambrini
- Mark M. Fuster
- Caroline M. Milner
- and others
Cited in Scopus: 64TNF-stimulated gene-6 (TSG-6) is a multifunctional protein secreted in response to pro-inflammatory stimuli by a wide range of cells, including neutrophils, monocytes, and endothelial cells. It has been shown to mediate anti-inflammatory and protective effects when administered in disease models, in part, by reducing neutrophil infiltration. Human TSG-6 inhibits neutrophil migration by binding CXCL8 through its Link module (Link_TSG6) and interfering with the presentation of CXCL8 on cell-surface glycosaminoglycans (GAGs), an interaction that is vital for the function of many chemokines.