DFG-funded CCRC Graduate Program (GRK 2407)

Research Training Group

Inflammatory and cellular stress signaling: Switches to vascular dysfunction

Cologne Cardiovascular Research Center; University of Cologne

Spokesperson of RTG: Stephan Baldus, MD
Deputy Spokesperson and scientific coordinator of RTG: Stephan Rosenkranz, MD

Details about the program

About the program:

  • Main Scientific Topic of the Program
  • Scientific Projects
  • Principal Investigators / Project Leaders
  • Core Facilities
  • CCRC and Framework of Graduate Programs at the UoC
  • Curriculum
  • Interdisciplinary Program Health Science (IPHS)
  • Selection process

Request for Reference Letter

Short description

Arterial vascular disease has long been considered as a state of adverse structural remodeling within arteries upon accumulation of circulating and vessel wall-derived cells, matrix, and cholesterol – histological hallmarks of atherosclerosis. However, more subtle alterations of vascular homogeneity and in particular vascular stressors have emerged as critical pre-requisites and drivers for a large spectrum of diseases. The major aim of our collaborative research training group (RTG) is to identify common vascular stressors and overlapping or redundant cellular signaling responses across a broad range of vascular disease entities. Our RTG welcomes highly motivated PhD and MD students to actively pursue cutting-edge research on individual, yet coordinated research projects, that are directly related to answering pertaining key questions for specific diseases in this research field. This RTG, embedded into the Cologne Cardiovascular Research Center (CCRC) aims to educate the next generation of cardiovascular researchers and to foster better understanding of the translational needs in this important medical area.

Core research idea and main research focus

Figure 3.1 Abberant cellular signaling and stress activators / responses in VASCULAR DYSFUNCTION, and their role in distinct clinical phenotypes. Illustration of the main focus of research projects on mechanistic insights (projects D, H, I) and/or disease-oriented models (projects A, B, C, E, F, G), creating multiple opportunities for collaborations within the CCRC-RTG, and enabling the identification of redundant mechanisms as well as multi-facetted basic research training for PhD/MD students.

The overarching aim of this interdisciplinary and collaborative research initiative is to unravel common underlying mechanisms linking inflammatory stressors and cell signaling responses in arterial vascular disease. The identification of critical and redundant stressors as well as pertaining cellular signaling pathways that propagate dysintegrity of the arterial bed should be a prelude to revealing potential therapeutic targets for a wide range of different vascular diseases (Figure 3.1). 

In this context, we will also consider mechanisms of inflammatory resolution. Since vascular dysfunction leads to a broad range of diseases and conditions, the expected gain of newly found knowledge and increased understanding should ultimately translate into the development of novel interventions, such as preventive paradigms, as well as new therapeutic options to treat vascular dysfunction in various organ systems and heart, lung and kidney in particular.

Available Core facilities

  1. Histopathology; Institute of Pathology (Büttner / Quaas)
  2. Proteomics; CMMC/CECAD Central Facility (Freese / Krüger)
  3. Molecular Imaging; Institute of Radiochemistry and Experimental Molecular Imaging, University of Cologne, and Forschungszentrum Jülich (Neumaier)
  4. Functional Genomics; Cologne Center for Genomics (CCG) (Nürnberg)
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