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Published on: March 2, 2016
HS and Inflammation: A Potential Playground for the Sulfs?
Rana El Masri1, Yoann Crétinon1, Evelyne Gout1
1Université Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale (IBS), Grenoble, France.
Extracellular sulfatases (Sulfs) regulate heparan sulfate (HS) structure and function by removing specific sulfate groups. This review explores the emerging role of Sulfs in inflammation and other physiological processes.
Area of Science:
- Biochemistry
- Cell Biology
- Glycobiology
Background:
- Heparan sulfate (HS) is a crucial polysaccharide involved in cellular signaling and processes.
- HS structure, particularly its sulfation pattern, dictates its interactions with signaling proteins.
- Extracellular sulfatases (Sulfs) are key enzymes that modify HS by removing 6-O-sulfate groups.
Purpose of the Study:
- To review recent literature on the role of Sulfs in inflammation.
- To expand the understanding of Sulfs beyond development and cancer.
- To highlight the potential of Sulfs in regulating new physiopathological processes.
Main Methods:
- Literature review of recent studies on Sulf family enzymes.
- Analysis of HS/ligand interactions and their modulation by sulfatases.
- Exploration of Sulf function in inflammatory contexts.
Main Results:
- Sulfs play a significant role in regulating HS biological properties.
- Previous research on Sulfs was limited to development and tumor progression.
- Emerging evidence suggests Sulfs are involved in inflammatory processes.
Conclusions:
- The role of Sulfs in inflammation is an under-documented but important area of research.
- Understanding Sulf-mediated HS modification opens new avenues for studying various diseases.
- Further investigation into Sulfs could reveal novel therapeutic targets.
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