Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis

Author:

Stojanović Stevan D12ORCID,Fiedler Jan1ORCID,Bauersachs Johann2,Thum Thomas1ORCID,Sedding Daniel G3ORCID

Affiliation:

1. Institute of Molecular and Translational Therapeutic Strategies (IMTTS), Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany

2. Department of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany

3. Department of Internal Medicine III, Cardiology, Angiology and Intensive Care Medicine, Martin-Luther-University Halle (Saale), Ernst-Grube-Strasse 40, 06120 Halle (Saale), Germany

Abstract

AbstractInflammation is a hallmark and potent driver of pathological vascular remodelling in atherosclerosis. However, current anti-inflammatory therapeutic strategies have shown mixed results. As an alternative perspective on the conundrum of chronic inflammation emerging evidence points towards a small subset of senescent cells as a critical player and central node driving atherosclerosis. Senescent cells belonging to various cell types are a dominant and chronic source of a large array of pro-inflammatory cytokines and various additional plaque destabilizing factors, being involved with various aspects of atherosclerosis pathogenesis. Antagonizing these key agitators of local chronic inflammation and plaque instability may provide a causative and multi-purpose therapeutic strategy to treat atherosclerosis. Anti-senescence treatment options with translational potential are currently in development. However, several questions and challenges remain to be addressed before these novel treatment approaches may enter the clinical setting.

Funder

Deutsche Forschungsgemeinschaft

Cluster of Excellence REBIRTH

Regenerative Biology to Reconstructive Therapy EXC 62

German Academic Exchange Service Graduate School Scholarship Programme

Foundation Leducq

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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