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Published on: May 6, 2014
HMGB1 in vascular diseases: Its role in vascular inflammation and atherosclerosis
A W S de Souza1, J Westra, P C Limburg
1Department of Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, The Netherlands. a.w.silva.de.souza@umcg.nl
Insights
High mobility group box 1 (HMGB1) is implicated in vascular diseases like vasculitis and atherosclerosis. Elevated HMGB1 levels correlate with disease activity, severity, and mortality in patients with vascular conditions.
Area of Science:
- Vascular Biology
- Immunology
- Biochemistry
Background:
- High mobility group box 1 (HMGB1) is a nuclear protein implicated in vascular disease pathogenesis.
- Elevated HMGB1 levels are observed in active systemic vasculitis (e.g., ANCA-associated vasculitis, Kawasaki disease) and atherosclerotic lesions.
Purpose of the Study:
- To review clinical and experimental evidence on the role of HMGB1 in vascular diseases.
- To explore HMGB1's involvement in inflammation, recovery, and remodeling post-ischemia.
Main Methods:
- Review of clinical studies assessing HMGB1 levels in patients with vascular diseases.
- Analysis of experimental models investigating HMGB1's function in ischemic injury and repair.
Main Results:
- Increased serum HMGB1 levels in active vasculitis and post-ischemic events (acute coronary syndromes, stroke).
- HMGB1 expression is upregulated in macrophages and smooth muscle cells within atherosclerotic plaques.
- HMGB1 levels correlate with disease severity and mortality in acute coronary syndromes and stroke.
Conclusions:
- HMGB1 plays a significant role in the pathogenesis and progression of various vascular diseases.
- HMGB1 is a potential biomarker for disease activity and prognosis in vascular conditions.
- Further research into HMGB1's mechanisms may reveal therapeutic targets for vascular diseases.
Abstract:
The nuclear protein high mobility group box 1 (HMGB1) has been suggested to be involved in the pathogenesis of several vascular diseases such as systemic vasculitis and atherosclerosis. In systemic vasculitides including ANCA-associated vasculitis and Kawasaki disease, serum HMGB1 levels are higher in patients with active disease compared to healthy controls. In atherosclerotic disease, HMGB1 displays increased expression in nuclei and cytoplasm of macrophages and smooth muscle cells in the atherosclerotic lesions, and is implicated in the progression of the atherosclerotic plaque. Experimental models of acute coronary syndromes and cerebrovascular accidents show that HMGB1 is not only involved in the amplification of the inflammatory response during acute ischemic injury, but also in the recovery and remodeling process after ischemia. Patients with acute coronary syndromes or stroke present significantly higher serum levels of HMGB1 than healthy controls and levels are associated with disease severity and mortality. Here we review clinical and experimental studies dealing with the role of HMGB1 in vascular diseases.
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