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Stem-Cell-Derived Circulating Progenitors Dysfunction in Behçet's Syndrome Patients Correlates With Oxidative Stress
Giacomo Emmi1, Amanda Mannucci2, Flavia Rita Argento2
1Department of Experimental and Clinical Medicine, University of Firenze, Firenze, Italy.
Frontiers in Immunology
|January 11, 2020
Summary
Behçet's syndrome patients have fewer circulating hematopoietic progenitor cells (CPC), which show increased oxidative stress and apoptosis. This dysfunction may impair vascular repair, contributing to disease progression.
Area of Science:
- Hematology
- Immunology
- Vascular Biology
Background:
- Behçet's syndrome (BS) is a systemic vasculitis linked to thrombotic events.
- Circulating hematopoietic progenitor cells (CPC) are crucial for vascular repair but are reduced in cardiovascular diseases.
- The mechanisms behind reduced CPC in BS and the role of oxidative stress are unclear.
Purpose of the Study:
- To investigate the relationship between circulating CPC dysfunction and oxidative stress in BS patients.
- To assess CPC number, oxidative stress markers, and apoptosis in BS patients compared to controls.
Main Methods:
- Quantification of CD34+/CD45-/dim and CD34+/CD45-/dim/CD133+ CPC subsets.
- Measurement of reactive oxygen species (ROS) and glutathione (GSH) levels in CPC.
- Assessment of caspase-3 activity as a marker of apoptosis.
Main Results:
- BS patients exhibited significantly lower CPC numbers compared to controls.
- CPC from BS patients showed elevated ROS levels and reduced GSH content.
- Increased caspase-3 activity was observed in BS patient CPC, indicating apoptosis.
- CPC number correlated inversely with ROS and positively with GSH content.
Conclusions:
- CPC in BS patients display oxidative stress and apoptosis, leading to reduced numbers.
- Oxidative stress-induced CPC dysfunction may impair vascular repair mechanisms.
- This dysfunction could contribute to the pathogenesis and progression of vascular disease in Behçet's syndrome.
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