A02-Danger signaling pathways in aortic disease

Chronic inflammation is responsible for the development and progression of aortic disease. In the first funding period, we demonstrated that specific activation of the innate immune system is critical for this pro-inflammatory state. Project A02 will expand on these findings by deciphering what cell types mediate the observed effects using conditional mice and specific in vitro models. For translation, we will test therapeutic interventions targeting innate immune receptor activation. Finally, we will study the role of danger signalling mechanisms of monocytes with specific pro-inflammatory genetic predispositions, termed clonal haematopoiesis of indeterminate potential (CHIP), in the development of aortic disease.

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© Sebastian Zimmer

Contacts

Avatar Zimmer

Prof. Dr. Sebastian Zimmer

Project leader A02

Heart Center, Building 26

Department Medical Clinic and Polyclinic II

University Hospital Bonn

Venusberg-Campus 1

53127 Bonn

Avatar Latz

Prof. Dr. Eicke Latz

Project leader A02

Biomedical Center II, Building 12, 1OG

Institute of Innate Immunity

University Hospital Bonn

Venusberg-Campus 1

53127 Bonn

Avatar Niepmann

Dr. Sven Thomas Niepmann

Postdoc

Heart Center, Building 26

Clinic for Internal Medicine II

University Hospital Bonn

Venusberg-Campus 1

53127 Bonn

Avatar Claeys

Saskia Claeys

PhD-Student

Biomedical Center I, Building 13, Floor 3, Room 14

Clinic for Internal Medicine II

Department of Molecular Cardiology

University Hospital Bonn

Venusberg-Campus 1

53127 Bonn

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