TSG-6: A multifunctional protein with anti-inflammatory and tissue-protective properties
Open accessAbstract
Tumor necrosis factor- (TNF) stimulated gene-6 (TSG-6) is an inflammation-associated secreted protein that has been implicated as having important and diverse tissue protective and anti-inflammatory properties, e.g. mediating many of the immunomodulatory and beneficial activities of mesenchymal stem/stromal cells. TSG-6 is constitutively expressed in some tissues, which are either highly metabolically active or subject to challenges from the environment, perhaps providing protection in these contexts. The diversity of its functions are dependent on the binding of TSG-6 to numerous ligands, including matrix molecules such as glycosaminoglycans, as well as immune regulators and growth factors that themselves interact with these linear polysaccharides. It is becoming apparent that TSG-6 can directly affect matrix structure and modulate the way extracellular signalling molecules interact with matrix. In this review, we focus mainly on the literature for TSG-6 over the last 10 years, summarizing its expression, structure, ligand-binding properties, biological functions and highlighting TSG-6's potential as a therapeutic for a broad range of disease indications.
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TSG-6 inhibits neutrophil migration to the injured site possibly by binding IL-8 and inhibiting neutrophil recruitment by this chemokine.
“TSG-6, an anti-inflammatory protein considered a key factor in immunomodulatory activity of MSCs [66], was shown to inhibit neutrophils migration to the injured site possibly by binding to IL-8 and, as such, to inhibit the neutrophils recruitment by this chemokine [67].”
From Mesenchymal stem cell secretome for regenerative medicine: Where do we stand? (2025) · cites this paper as [67]
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Mesenchymal stem cell secretome for regenerative medicine: Where do we stand?
Trigo, C. M., Rodrigues, J. S., Camões, S. P., Solá, S., & Miranda, J. P. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2024.05.004 · Cited by 205 · see citing works
- Authors
- Day, A. J., & Milner, C. M.
- Affiliations
- Manchester Academic Health Science Centre (GB)
- Corresponding author
- Day, Anthony J.
- Venue
- Matrix Biology
- Publisher
- Elsevier BV
- Published
- 2019-05
- Volume
- 78-79
- Pages
- 60-83
- ISSN
- 0945-053X (ISSN-L)
- OpenAlex
- W2783235617
- Cited by
- 306
- References
- 0
- Citations by year
- 2026: 17 · 2025: 37 · 2024: 51 · 2023: 42 · 2022: 42 · 2021: 50 · 2020: 36 · 2019: 21 · 2018: 9
- FWCI
- 3.26
- Type
- journal article
- Language
- en
- Open access
- Licence
- Locations
- Matrix Biology (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (acceptedVersion, other-oa)
- Funders
- Arthritis Research UK (20895, 21946)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
- Keywords
- TSG-6, anti-inflammatory proteins, tissue protection, mesenchymal stem cells, immunomodulation, glycosaminoglycans, extracellular matrix, ligand binding, therapeutic potential
- MeSH terms
- Animals, Extracellular Matrix, Glycosaminoglycans, Humans, Models, Molecular, Protein Binding, Protein Conformation, Signal Transduction, Cell Adhesion Molecules, Intercellular Signaling Peptides and Proteins, Mesenchymal Stem Cells
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