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- Milner, Caroline MRemove Milner, Caroline M filter
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Please choose a date range between 2015 and 2020.
Author
- Day, Anthony J3
- Birchenough, Holly L2
- Briggs, David C2
- Enghild, Jan J2
- Jowitt, Thomas A2
- Ali, Tariq1
- Baldock, Clair1
- Dyer, Douglas P1
- Fuster, Mark M1
- Handel, Tracy M1
- Ievoli, Elena1
- Johns, Scott C1
- Kielty, Cay M1
- Langford-Smith, Alexander WW1
- Richter, Ralf P1
- Rugg, Marilyn S1
- Salanga, Catherina L1
- Salustri, Antonietta1
- Valdambrini, Elena1
- Waltho, Jon P1
Keyword
- hyaluronan2
- reproduction2
- cell migration1
- chemokine1
- chemokine-binding protein1
- CUB module structure1
- cumulus-oocyte complex expansion1
- extracellular matrix1
- glycosaminoglycan1
- heavy chain-hyaluronan complex formation1
- heparan sulfate1
- heparin-binding protein1
- inflammation1
- innate immunity1
- inter-α-inhibitor1
- Inter-α-inhibitor Heavy Chain1
- protein stability1
- protein structure1
- protein-protein interaction1
- proteoglycan1
- site-directed mutagenesis1
- small-angle X-ray scattering (SAXS)1
- TNF-stimulated gene 6 (TSG-6)1
- TSG-61
- X-ray crystallography1
Glycobiology and Extracellular Matrices
3 Results
- Glycobiology and Extracellular MatricesOpen Access
Inter-α-inhibitor heavy chain-1 has an integrin-like 3D structure mediating immune regulatory activities and matrix stabilization during ovulation
Journal of Biological ChemistryVol. 295Issue 16p5278–5291Published online: March 6, 2020- David C. Briggs
- Alexander W.W. Langford-Smith
- Holly L. Birchenough
- Thomas A. Jowitt
- Cay M. Kielty
- Jan J. Enghild
- and others
Cited in Scopus: 12Inter-α-inhibitor is a proteoglycan essential for mammalian reproduction and also plays a less well-characterized role in inflammation. It comprises two homologous “heavy chains” (HC1 and HC2) covalently attached to chondroitin sulfate on the bikunin core protein. Before ovulation, HCs are transferred onto the polysaccharide hyaluronan (HA) to form covalent HC·HA complexes, thereby stabilizing an extracellular matrix around the oocyte required for fertilization. Additionally, such complexes form during inflammatory processes and mediate leukocyte adhesion in the synovial fluids of arthritis patients and protect against sepsis. - 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: 70TNF-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. - Glycobiology and Extracellular MatricesOpen Access
Metal Ion-dependent Heavy Chain Transfer Activity of TSG-6 Mediates Assembly of the Cumulus-Oocyte Matrix
Journal of Biological ChemistryVol. 290Issue 48p28708–28723Published online: October 14, 2015- David C. Briggs
- Holly L. Birchenough
- Tariq Ali
- Marilyn S. Rugg
- Jon P. Waltho
- Elena Ievoli
- and others
Cited in Scopus: 38Background: TSG-6 (TNF-stimulated gene-6)-dependent transfer of heavy chains from inter-α-inhibitor onto hyaluronan is critical for ovulation.Results: A calcium ion and chelating glutamate within TSG-6 mediate formation of the covalent heavy chain-TSG-6 intermediate.Conclusion: TSG-6 transferase activity rather than hyaluronan binding drives cumulus expansion.Significance: The role of metal ions in hyaluronan-heavy chain formation has been determined.